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Questions related to Google
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The desktop in which this software was installed got crashed and we are left with no options.
I have googled it, but was not able to find the compatible software.
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Did you get any response for this question? We have the same issue with an AlphaImager 2200.
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In order to conduct a pre-post experiment to see the effectiveness of problem-solving therapy on university students, their quality of life was assessed using the WHOQOL-BREF google survey questionnaire. Data was exported from google spreadsheet to excel and then spss. Should four different spss files be made out of which two will be for the control group before and after and the other two for the experimental group before and after? I have totaled the domain scores before entering data on spss, but I think that wasn't necessary.
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It is not necessary to create four different SPSS files for this study. Instead, you can use a single SPSS file to store all the data and use different variables to differentiate between the experimental and control groups, as well as the pre and post measurements.
It is also not necessary to total the domain scores before entering the data in SPSS. You can enter the individual item responses for each participant and then use SPSS to calculate the domain scores by adding up the item scores and dividing by the number of items in that domain. This will allow you to have more detailed data to analyze if needed.
Here are some general steps you can follow to analyze the data in SPSS:
  1. Enter the data for all participants, including their group (experimental or control) and the time of measurement (pre or post).
  2. Use descriptive statistics to examine the distribution of the data, including means, standard deviations, and frequencies.
  3. Use inferential statistics (e.g., t-tests or ANOVA) to compare the mean scores between the experimental and control groups and between the pre and post measurements.
  4. Use regression analysis to examine the relationship between the independent variables (group and time) and the dependent variable (quality of life scores).
  5. Finally, interpret the results and draw conclusions about the effectiveness of problem-solving therapy on university students' quality of life.
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Dear managers,
Today I found out that I have one real profile and the second is fake. What should I do?
It almost does not have my articles. Somebody created it recently. What should I do?
With respect, Oleg Kharchenko
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https://www.researchgate.net/profile/Oleg-Kharchenko may be an older profile than https://www.researchgate.net/profile/Oleg-Kharchenko-2. See this instruction how to merge duplicate profiles: https://explore.researchgate.net/display/support/Duplicate+profiles. If this will no work, you may try to contact RG's support team at https://www.researchgate.net/contact. (Please note that you did not write to the managers, but to ResearchGate's community.)
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I wondered whether or not the selection of articles and documents proposed by ResearchGate was based on Boolean logic and with, more or less, the same logical operators as Google
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To me it seems that at the moment not even an AND-search works (no matter whether "AND" is actually used, or not). Some weeks ago, I searched for <conceptual AND skills AND psychotherapy> and got 79 results. When I do it again now, I get 100 results pages, i.e. 1,000 results, but 90% of the results do not contain all three search words. Does anyone know, whether ResearchGate has changed its search function and how one can actually perform and AND-search?
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According to PRISMA, you need to remove duplicate items before screening. However, google scholar will give you about 10 times of results than the databases (Scopus, Web of Science, etc).
It is literally not possible to add all items to Zotero either via connector or scraper, as Google will ban your IP after about 400 results.
However, doing screening first seems to violate the PRISMA guideline.
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Unless things have changed very recently, downloading from Google Scholar is very tedious, so it is rare to see it included in published accounts of systematic searches. I suggest you rely on Web of Science and Scopus, because the main things that you will miss by not including Google Scholar are book chapters, plus "gray literature" such as theses and conference presentations,
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I received an email this morning from an address ending in "@sciencepostnetwork.com". They ask me to provide links to my publications so they can create news stories that can be published in many digital media. Here is an excerpt from the email:
"As Google news receives millions of hits each day from a broader audience including professionals and students, only a few exceptional researchers are selected and invited to submit their work, and you are invited! We are a specialist agency "Scientific Media" working within the research community to produce high-value, impactful communications content for researchers. This content is made available to a broad global audience and distributed to over 500+ premium news sites including Google News, Google News, WND, Bing News, Ask, CBS, CNN, Bloomberg & More, which also include key research community actors, research peers, government figures, funding agencies, policy makers, NGOs, charities, schools and libraries, investors and commercial entities, and many more"
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They look like a scam. That's why I didn't do anything with them.
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I have seen both terms being used in manuscripts and googled the question but did not get a clear answer
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In studies of drugs/interventions, a "vehicle" and a "placebo" are not interchangeable terms.
A vehicle is a substance used as a carrier or solvent for a drug or intervention that is being tested. It is intended to be inert and not have any therapeutic effect of its own. A vehicle is often used as a control in studies to ensure that any effects observed are due to the drug/intervention being tested and not the carrier substance.
On the other hand, a placebo is a substance that is designed to look and feel like the drug/intervention being tested, but is actually an inactive or inert substance. The use of a placebo is intended to control for the placebo effect, which is a psychological effect where patients experience an improvement in symptoms simply because they believe they are receiving an effective treatment.
So while both a vehicle and a placebo may be used as controls in studies of drugs/interventions, they are not interchangeable terms. A vehicle is a carrier substance that is inert and intended to have no therapeutic effect, while a placebo is an inactive substance designed to look and feel like the drug/intervention being tested in order to control for the placebo effect.
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Is it useful to manually profile a conference paper that is not recognized and indexed by Google?
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According to my personal experience: posting papers on Academia.edu platform shortening the period for recognition of your paper by Google Scholar crawl... Good luck!
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I was approached via email (marketing flavour), and after some googling could not find out if they are a legitimate organization/enterprise(??).
Any information based on personal experience is appreciated.
Thank you!
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SciPinion is a network of experts, see https://scipinion.com/about/. I am generally sceptical when receiving such invitations and ignore them.
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We recently published a book. We have an ISBN for it. However, I am not sure how to track citations of the book digitally (e.g. Google Scholar). I saw an entry where it suggest uploading the file to Google Books as "Documents that exceed 5MB in size will not be indexed by Google Scholar’s search robots". But we do not want to upload the whole book there.
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Thank you Madeleine!
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So, I'm looking to evaluate the mRNA expression of an enzyme produced by bacteria in human feces. In this case, the idea was to isolate the bacterial RNA and perform an RT-qPCR of the enzyme. However, we are not supported designing a primer that aligns with the genome correctly and we also did not find any paper that did this
📷
Abrir no Google Tradutor•
Feedback
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Unfortunately, I am not able to design the primer. I end up making the entire genome of the bacteria and not just the protein
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How do I cite a Google Street View (GSV) Image in a journal ?
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As far as I know, Google has the copyrights of its GSV images, and you cannot use such an image without permission. If they will give permission upon request, they may also indicate how to cite it. In case of images of other owners, I got such instructions.
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Hello dear RG community.
I'm doing PIV in water with red fluorescent 8 micron polystyrene PIV particles (Fischer catalog number 36-3B https://www.thermofisher.com/order/catalog/product/36-3B).
I have a problem adding them to water. The moment they touch the water surface, they, first, lump together, second, stay on the surface.
It's very tedious to break the lumps and submerge the particles mechanically (i.e. manually with a stick).
I'm wondering if there is a way to get the particles in water without those issues.
Thank you in advance.
Ivan
P.S. I have noticed an uptick of spam in the threads recently. For instance, people would post "following" as a reply, or just copy-paste google search. I'm sorry, but if such replies occur in this thread, I will delete them.
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Perhaps a little detergent would help, such as Triton X-100 or Tween-20, which are commonly found in bio labs. The surface of the beads is presumably very hydrophobic, so detergent should help them interact favorably with water.
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Hello everyone,I am trying to find out embeddings of drug dataset which i had downloaded on moleculenet.org using graph autoencoder.But everytime i got errors.I have tried many ways to do it.But everytime i got errors.So,can anyone help me to do this task.My dataset contains some invalid smiles also but that's not the issue.So, please help if anyone can.I attach the csv file and the google colab link where my codes are written with this question.It's my humble request to please help me if anyone can.
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Souvik Panda I'm delighted to hear you're attempting to identify embeddings of a drug dataset from MoleculeNet using graph autoencoders. However, it appears that you've been experiencing some difficulty with mistakes.
The first thing I would suggest is double-checking the input data to ensure it is in the right format. SMILES strings, which are a standard technique of describing chemical structures as strings, should be present in the CSV file you mentioned. The smile strings must be proper, and invalid smiles must be handled individually.
It's also critical to ensure that any pre-processing tasks, such as converting SMILES strings to graphs, are carried out appropriately. RDKit, a prominent open-source toolkit for cheminformatics, is one library you may utilize for this.
Regarding the Colab link you provided, it's impossible for me to assist without seeing the precise code and issues you're having. If you're still having problems, I recommend asking a query on a site like Stack Overflow and including the exact error message and traceback. You should also consider posting in the Moleculenet community or forums connected to cheminformatics or graph neural networks, where other academics working on comparable problems may be able to assist you.
It's also worth noting that there are multiple pre-trained models available on the MoleculeNet repository, so instead of training your own, you might try utilizing one of them as a starting point.
Finally, I recommend double-checking your code to ensure that you are using the right version of the packages and that your dataset is properly loaded. Small errors in the code can sometimes cause huge problems, and fixing them may solve the situation.
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Suppose I faced a series of very rare cases of pediatric patients, and I decided to conduct a study on the their parents to try to know the risk factors and psychological negative consequences on them because of their children got this rare infection. If i send them through WhatsApp a google form survey.
My question is what is the name of the method i used ?
is it “A case series design targeting the parents“ or is it “ retrospective study“
below what I already have written
“ A case series design was employed in the study. The design is often employed in the description of characteristics and outcomes among individuals who have a disease or exposure [8]. In this case, the focus was on parents whose children had been exposed to this rare infection “
8. Torres-Duque, C. A., Patino, C. M., & Ferreira, J. C. (2020). Case series: an essential study design to build knowledge and pose hypotheses for rare and new diseases. Jornal Brasileiro de Pneumologia, 46(4), e20200389. https://doi.org/10.36416/1806-3756/e20200389
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Does anyone know what the pore size of Corning® Matrigel® hESC-qualified Matrix is? I have tried searching for the information sheets of this product but to no avail and other google searches (unless I have missed it). Anyone that could help me with this?
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I think Matrigel is sterile filtered during isolation (0.2 um).
Biggest molecule inside is laminin-111 sized 800 kDa in native condition.
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I have tried to implement smote on a drug dataset's embedding on 7 different classifiers but can't find improvement of the result of the 6 classifiers.Is this my system's fault or any other issue may be happen.Please help
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Souvik Panda SMOTE (Synthetic Minority Oversampling Strategy) is an oversampling technique for improving machine learning model performance on unbalanced classification problems. Here are a few things you may attempt to improve SMOTE's performance on Google Colab:
1. Use a larger dataset: Using a larger dataset is one technique to boost SMOTE performance. This can assist SMOTE to create more varied synthetic samples, which can increase your model's generalization ability.
2. SMOTE's hyperparameters can be adjusted: SMOTE features numerous hyperparameters that can be adjusted to regulate the oversampling process. You can, for example, vary the percentage of synthetic samples created or the number of nearest neighbors utilized to generate the synthetic samples. You may experiment with various combinations of these hyperparameters to find which one provides the greatest performance.
3. Ensemble approaches, such as boosting and bagging, can increase SMOTE performance by training numerous models and aggregating their predictions. You may use ensemble approaches with SMOTE to determine whether they help your model perform better.
4. Use other oversampling techniques: You can use additional oversampling techniques in addition to or instead of SMOTE. Try the ADASYN (Adaptive Synthetic Sampling) or the Borderline SMOTE algorithms, for example. You may compare their performance to find which one works best for your dataset.
I hope these recommendations are useful! Please let me know if you have any more inquiries.
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What should I do to make the Researchgate full-text work appear on google academic as well?
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Thank you for your answer
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First of all, I have narrow knowledge about antidiabetic assay as this is my first enzymatic test and I have no one to refer. I have a method but when I tried to google every each of the method detailed, the result showed that most of the method used a-glucosidase in solid form (mostly brand Sigma Aldrich) but mine was in liquid form from this brand (https://www.megazyme.com/alpha-glucosidase-yeast-maltase). The things is, I tried to study about unit of enzyme. But turn out to be quite complicated since it include activity, time, mass and so on.
Here is the method I referred:
Can someone assist me on this? Any suggestion on method modification are welcomed.
Notes:
1. Sample: polyherbal extract
3. Acarbose will be used as a positive control at varying concentrations(12.5 to 400 μg/mL)
4. Will used Biotek multi-well plate reader
Thank you.
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The product is supplied as a suspension at 1000 U/mL. You will have to dilute it a thousand-fold (final concentration in the assay) with the assay buffer since the paper you cited used it a 1 U/mL, assuming the specific activities and unit definitions are similar for the product you purchased and the one cited in the paper. Performing some preliminary experiments to test a range of enzyme concentrations would be a good idea.
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I have added a new entry "Analyse und Optimierung der Schaumschlackenfahrweise eines Gleichstrom-Elektrolichtbogenofens mittels Machine Learning Verfahren". It is a printed book. Unfortunately I did not find how to make this entry visible on google or google scholar. I would be grateful for your feedback and efforts.
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Thank you a lot Dr. @Wolfgang R. Dick for your feedback. I think you are right because when I Google my Name in combination with ResearchGate only my old academic degree is displayed in the search results.
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Does anyone know what happened to CETI, a journal of petroleum engineering and geoscience, published out of Calgary, Alberta? Can no longer find the title or any of the papers published therein with a Google search.
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Indeed, using CETI and journal renders virtually nothing in Google. It appears that the magazine no longer exists (what I found is some papers between 2012-2016) and the website www.ceti-mag.ca no longer is active.
However, if you search for one of the following search items:
Canadian Energy Technology and Innovation journal
ISSN 1929-7408
It renders some hits in Google (also look at Images) and Google scholar. As far as I can see it use to be a magazine with nicely edited papers (see enclosed file for an example). However, I doubt the originality of the content, it looks to me that most of the papers are re-edited papers published earlier in for example conference papers, just have a look at:
Experimental Investigation of Wet Gas Dew Point Pressure Change With Carbon Dioxide Concentration
Best regards.
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Dear Researchers,
Has anyone noticed after the launch of ResearchGate new design & look that Google Scholar is not indexing papers only uploaded on Research Gate? Hence, most of your new citations on Google Scholar are from Journals published online and articles uploaded on repositories (including Open Archives and Institution Repositories) only.
New citations traced on ResearchGate for the conference papers and preprints uploaded on ResearchGate are not being traced or indexed on Google Scholar. Fulltext uploaded on ResearchGate cannot search over Google Scholar. Still, at the same time, these publications are searchable on the Google search engine.
Do you have any solution to this issue, or do we need to wait until ResearchGate resolves it?
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Wolfgang R. Dick Thank you Sir for your response.
I have gone through previous discussions, and it seems RG changed its design recently in November, then onwards, RG contents are not indexed on Google Scholar. It seems to be a "crawlers" issue with the new design, misconfiguration, or maybe a metadata issue within the new RG.
Yes, technically RG can resolve this issue by allowing Google Robots exclusion protocol.
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I am working with an International Academic publisher named UniversePG have nine (9) journals.
When we search articles on Google sometimes a few articles' contents are not found in Google/Google Scholar !
We want to solve this error/problem as early as possible.
So, waiting for your instructions and guidelines with a reply !
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Dear, maybe your article's DOI number is not valid or your published journal is not indexed in the database.
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1) whenever I run md in google colab ( free) ,I have to always run the md installation command again and again.And in between as session is interrupted the gromacs automatically gets deleted , so here also i have to run the whole gromacs installation nd commands again.any solutions to this?
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Hello every one
Any one know how to use Google Cloud AutoML Vision based on Johnsen scores.
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Dear Waseem Ali Vistro,
You may want to review the data presented below:
AutoML Vision API Tutorial
This tutorial demonstrates how to create a new model with your own set of training images, evaluate the results and predict the classification of test image using AutoML Vision.
The tutorial uses a dataset with images of five different kinds of flowers: sunflowers, tulips, daisy, roses and dandelions. It covers training a custom model, evaluating model performance, and classifying new images using the custom model.
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Google Cloud AutoML Vision for Medical Image Classification
Pneumonia Detection using Chest X-Ray Images
The normal chest X-ray (left panel) shows clear lungs without any areas of abnormal opacification in the image. Bacterial pneumonia (middle) typically exhibits a focal lobar consolidation, in this case in the right upper lobe (white arrows), whereas viral pneumonia (right) manifests with a more diffuse “interstitial” pattern in both lungs. (Source: Kermany, D. S., Goldbaum M., et al. 2018. Identifying Medical Diagnoses and Treatable Diseases by Image-Based Deep Learning. Cell. https://www.cell.com/cell/fulltext/S0092-8674(18)30154-5)
Google Cloud AutoML Vision simplifies the creation of custom vision models for image recognition use-cases. The concepts of neural architecture search and transfer learning are used under the hood to find the best network architecture and the optimal hyperparameter configuration that minimizes the loss function of the model. This article uses Google Cloud AutoML Vision to develop an end-to-end medical image classification model for Pneumonia Detection using Chest X-Ray Images.
Table of Contents
  • Pneumonia Detection using Chest X-Ray Images
  • About the Dataset
  • Part 1: Enable AutoML Cloud Vision on GCP
  • Part 2: Download the Dataset to Google Cloud Storage
  • Part 3: Preparing the Dataset for Modeling
  • Part 4: Modeling with Cloud AutoML Vision
  • Part 5: Testing the Model
  • Part 6: Conclusion
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Has anyone considered computationally (e.g., Google site mining) identifying repeat patterns in publishing sites, building a site-similarity rank index, then letting millions of scholars judge for themselves? Most of these sites are clones of bulk predatory publishers (i.e., they self-plagiarize their sites, because doing otherwise is not as profitable as slumlording). Legitimate ones are far more unique.
I just Google-searched "Submission of a manuscript implies that authors have met the requirements of the editorial policy" (a string I selected from twasp.info/journal). Dozens (hundreds? thousands?) of sites popped up. There's no Jeff Beale to attack in such a model, because scholars are only confirming or rejecting given sites.
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Dear Peter Zelchenko , I was informed today that my contribution to your research question was deleted by Researchgate officials. They claim that I have broked RG terms of services. My contribution was about ResearchLeap publisher!!!
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My Google Scholar profile is public but it does not appear in google's search result. How can I fix this problem? When i write my name Sajid Ur Rahman in google search it shows research gate and frontiers loop profile but not google scholar profile. Here is the link to my google scholar profile (https://scholar.google.com/citations?hl=en&user=UmHOSlMAAAAJ)
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Lockdowns due to the COVID pandemic in last three years (2020-22) has played a significant role in the widespread of online based classrooms using applications like Zoom, MS teams, Webex and Google Meet. While substantial amount of the students were happy to complete their semester classes in due time without getting hampered by the lockdowns, thanks to the online based classrooms, there are also notable amount of students and parents who were complained regarding the online based classrooms that they have drastically distracted the academic performance of students.
Overall, I would like to leave it as an open-ended question. Dear researchers, what you think regarding the online based classroom? Is it an advantage for students or a disadvantage?
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Online-based classrooms are necessary for circumstances where the learners and teachers feel that the knowledge can be catered to without meeting in person. It is an opportunity for learners to learn at their doorsteps. Nonetheless, online classes are not as effective as offline classes for many learners who take education as a social process where peer learning, group dynamics, and interpersonal relationship are of high importance. Online class doesn't provide the experience of personal interaction while learning.
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Hello my research group developed a website that utilizes google sheets to automatically calculate, sort and produce a graph of the bmi classification of the students. Is there any testing method we can reference from to compare our research to the usual calculation of bmi which utilizes pen and paper?
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I am in doubt what it is you are looking for. Are you looking for OTHER ways than BMI, or are you looking for a tool which can carry out parts of the data collection + transfer to Google Sheets? It is a bit unclear which part you want to optimize on the process. I understand that you are searching for a faster method - but - for what? Please elaborate on this and I may be able to assist you. It will not cost you anything.
Sincerely
David Svarrer
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Dear All greetings! I was studying a paper describing combining ability. I found the word per se value, per se performance. I searched on google but did not get a satisfactory answer. Can anyone cooperate?
Thank you.
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The mean performance of the parents
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Hi. I am looking for the Hansen solubility parameters of aminated polysulfone (aPSU). I looked for these data in Google, unfortunately I couldn’t find it. I would be very grateful if you can help me to define these parameters value. I also was wondering which green solvent you propose for dissolving aPSU?
Thank you
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Dear Majda,
You can use HSPiP to measure the solubility parameters of aminated polysulfone. Just wanted to know, is it a regular and linear polymer?
Another way to measure the solubility parameters are performing solubility experiments.
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This may sound like a chicken and egg problem as new questions are usually based on previous answers. In my understanding, nowadays that many answers could be found via simple googling, asking (novel and good) questions are more important as they could hardly be generated by artificial intelligence. On the other hand, providing useful answers to such questions is challenging as well. What is your opinion?
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Aryan Shahabian: Agree with the above answers to the question! A question leads to one answer but an answer leads to at least 10 questions. Mustafa.
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...could not find it when googling :(
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📢 IEA EBC Annex#81 calls for datasets of B2G services: The Annex#81 subtask C3 team is coordinating a survey to collect open datasets for building-to-grid services (B2G) and would like to kindly ask you to contribute by providing a description and link to your data using this Google Form (https://docs.google.com/forms/d/e/1FAIpQLSdqV6MxY0DiJUar9kdkXypXq7EhuhxLP9OzHaN7WjZ9xlFaOg/viewform). 🔖 This survey aims to collect data (time series and metadata) from buildings performing demand-response, demand-side management or energy flexibility. The dataset may be from existing, simulated, or semi-simulated hardware-in-the-loop buildings. The collected datasets will be used for: ➡️ Gathering use cases and assessing typical DR strategies, buildings types, energy systems and data requirements, ➡️ Testing energy flexibility KPIs for the review activity of C3 on existing KPIs for B2G services, ➡️ And, possibly, comparing the existing solutions against “grid challenges” from the proposed C3 web-based showcase platform. ⌛️This survey should take approximately 20-30 minutes to complete. Thank you in advance for your valuable contributions! Don't hesitate to share that post. Feel free to reach us (Hicham Johra: hj@build.aau.dk; Flávia de Andrade Pereira: flavia.deandradepereira@ucdconnect.ie) if you have any questions. #Annex81 #survey #dataset #B2G #KPIs #DR #DSM #datadriven #smartbuildings #flexibility #metadata #datarequirements
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Thanks for your answer. Please, send me an email hj@build.aau.dk and I will forward you the questions directly by email.
Thanks for your help
/Hicham
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I am creating FEA model by abaqus. But I can not find epoxy property . When I get this property in google ,youtube ,researchgate then I can not understanding it.
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Dear Ibrahim,
A brief explanation is given in this paper:
DOI: 10.1016/j.compscitech.2021.109117
You can study Chapter 4 of Christian Breite's PhD thesis on "characterisation & mechanical modelling of epoxy resins" for a comprehensive explanation.
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Hi,
I am wondering-is it possible to buy a ready made mix of acids for the SCFA supplement (acetic, propionic, butyric and isovaleric acid)? I need to prepare a bacterial culture medium and this supplement is a pain. Tried googling, but could not find a vendor.
Thanks!
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Well the recipe is several pages long, so I am not sure if it makes sense to go over that:). My only concern is whether the SCFA supplement needs to be made or can be bought. If you make it out of salts, can you please suggest the protocol that you use for that?
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Hallo everyone,
Does anyone know some other type of mechanisms(except the mostly known ESCRT machinery or the recently studied SM dependent membrane repair of lysosom from Niekamp et al. 2021)used to recovery the minor disruption of lysomal membrane? I did honestly much Google research but I couldn't find more other different as those two system.
Thanks in advance!
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Recycling the lysosomal membrane protein.
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I'm working on the modal analysis of a cracked rectangular plate and come across an error. A sketch of the model is shown in the attached graph. I use KSCON command to model the stress concentration at the crack tip. When the crack length is small, everything is fine and I can get results. However, when the crack length is medium, say 0.2 times the crack width, I get this error:
*** ERROR *** CP = 3.125 TIME= 11:12:56
The stress concentration element generation will interfere with the
area's boundary.
I tried making the mesh even finer and the error was still there. I googled it and didn't find any information regarding this error. Does anyone have this error before? Is there a way to avoid it?
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Just a follow-up. The error can be avoided by making the crack like a V shape. Essentially the idea is to separate the two sides of the crack. For natural frequency calculation, a tiny V shape has little influence over the final results.
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Do you think google forms can replace the traditional structured questionnaire?
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Undoubtedly, Google Forms is a better and easier medium for primary data collection in this technological age.
But, sometimes relying solely on Google Forms is harmful because with the help of Google Forms, we can reach only those people who have communication tools while the other part has nothing to do with it.
Hence there is a need of some pilot survey for some quality checks and take a realistic picture.
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Hi! Trust this message meets you well. I am currently doing a research on the effect of tax amnesty on the tax compliance behavior of Nigerian taxpayers. As a result, I would require your help as you take some minutes to fill this online questionnaire. It is purely for research purpose and all information provided will be treated with utmost confidentiality. Please use the link below to proceed to the google form (use chrome preferably) Thank you for your time. https://forms.gle/J2kCRPXfsuzS4oReA
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If the state works to exempt taxpayers by reducing red tape, it will reduce tax evasion and increase compliance
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Hi. Currently, I have two problems when using Google Scholar (GS). I hope someone can give me some advice:
  1. I still can't find my GS profile, although I made it public before
  2. GS doesn't count my citations correctly. I can see missing at least some citations from a paper published 10 months ago (not sure for others)
Do you have ideas on how to fix that issues? It seems no realizable contact information for Google.
Thank you so much!
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Dear Thong Minh Trinh That is a slightly different question. Have a look at: https://www.researchgate.net/post/Google_scholar_profile
Conclusion: Patience (the GS profile of the person asking the question is now perfectly visible in Google itself).
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Millions of peoples round the world using internet and media for communication and google for search ,the virtual world is dominating the real world .How can we determine the real and true information s and facts not false knoledge?
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Dear Head of Dep. Prof. Alasadi!
You raised a very important topic to discuss. Cross-checking information available on multiple online platforms could be a starting point. Background research on the topic as a whole could add certainty.
I found some materials on this issue:
1) J. Jeyasudha  · Prashnim Seth  · G. Usha  · Pranesh Tanna. Fake Information Analysis and Detection on Pandemic in Twitter, SN Computer Science (2022) 3:456 https://doi.org/10.1007/s42979-022-01363-y Free access:
2) Li, J., Chang, X. Combating Misinformation by Sharing the Truth: a Study on the Spread of Fact-Checks on Social Media. Inf Syst Front (2022). https://doi.org/10.1007/s10796-022-10296-z, Free access:
3) Vraga, E. K., & Bode, L. (2022). Correcting What’s True: Testing Competing Claims About Health Misinformation on Social Media. American Behavioral Scientist, 0(0). https://doi.org/10.1177/00027642221118252, Available at: https://journals.sagepub.com/doi/abs/10.1177/00027642221118252?ai=1gvoi&mi=3ricys&af=R
Yours sincerely, Bulcsu Szekely
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I have a published paper under Common Ground Scholar Network (CGS) in 2021. The DOI is https://doi.org/10.18848/2470-9247/CGP/v06i03/1-14.
However, my paper is still not reflecting in the google scholar. I asked the CGS team and I was told that they had no power on when articles appear in Google Scholar. Though the CGS provided access to Google bots, to transfer the data , they cant be of much help when it comes to publishing. Could I get any assistance on how to make my publication appear specifically in Google scholar?
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No problem, add your published article to your Google Scholar profile manually.
In other words, via your profile go the (+) sign and then select add article manually.
Good luck.
Regards,
Emad
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When I upload new PDF files they are usually found within a couple of days by Microsoft Bing but might be by Google after a few months - WHY?
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Does we consider "upload" as an action within RG platform?
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I wish to find the doi of the article from journal's name, volume, and page. I believe that these information can uniquely determine the article ID (DOI). But as far as I searched with Google, no useful information is available. Google Scholar is not so convenient from this viewpoint. For me, it is tedious to repeat going to the journals' homepage and enter the vol. and pg. Thanks in advance for your kind suggestion,
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Takayuki Makino : This is indeed a problem, especially when the reference is not given correctly. Several years ago I read a study how many references in publications contain errors. I do not remember the percentage, but the number was rather high. Titles give redundancy and make the search easier, but in many journals these are omitted.
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I was gathering data about Arsi University Bekoji campus, and I observed something about the city planning. On the right side of the google image (in 2019), you can see the new urban development, and on the left side, what is most probably agricultural villages and Greenfield. The new urban development follows one of the typical city plannings I have seen all over Ethiopia, which follows a grid pattern to arrange the urban blocks and in contrast, the Greenfield has its own block pattern, which I think is the result of the social, cultural, and historical way of arranging plot of lands. It shows the trails of what is left of the ‘traditional planning.’ My whole point here is, why don’t the city planners appreciate and try to incorporate the traditional/ unexplored knowledge into the planning. That way, each city can have a unique experience and preserve the inhabitants’ lifestyle. Of course, my assumptions might be wrong, so if you are from, visited, or lived in Arisi, I would like to know what you think? Or let me know what you think about the planning ? About Arsi: Location: Bekoji, Arsi zone, Oromia region, Ethiopia Population as of 2015: 181, 906 Built-up area: 0.76 sq. km google map: https://lnkd.in/g74-VAm5 #arsi #bekoji #arsiuniversity #agriculturalvillages #savetraditionalplannings
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Some 40 years ago I worked with multi-disciplinary teams from various European consultants on town and area development plans. My impression now is that we were exporting skills which perhaps did not include any awareness of local / traditional development concepts. I would be interested to know if anyone has a set up a library of examples from different countries and cultures.
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Hellow every body, we are making a research related to covid-19, put we are not able to reach Emirati people
Could any of you help us to reach them, to collect the data by a google form, and his name will be included as a collaborator in the research.
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Hello. I thought you were Lebanese. Why are you working on Covid-19?
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How to make google colab pro run faster with image dataset. I am already using with google-drive but it is too slow?
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Ajay Krishan Gairola Are you getting slower performance when you train the model or when you load the data? Perhaps you should use Tensorflow 2.0 data pipeline which is specifically optimized for such scenarios.
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Before this, a pink streak was seen on the media. But, after few days, the streak changed to small dots and the line diminished. I have tried googled some answers, but can't find any. I'm a newbie in microbiology field, so I hope to get a simplified, easy to understand answer. Tysm
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Contamination due to swarmming of Bacillus subtilus enter in your plate
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Hello everyone,
I googled the sequence of plasmid pFD340 and found no one had posted the sequence of the plasmid. I wonder who could kindly provide it and I really appreciate it. I know I could get it sequenced, however, it will take around two weeks to one month and now it is holiday season.
Thanks a lot.
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Hi, I have considered use this pfd340 plasmid in my research, but I could not find a company buying this. Would you mind telling me where you get this pfd340 plasmid? Your support is greatly appreciated.
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I want to use image dataset (that is stored in my personal computer) in google colab. Please help.
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Hi, you can use a dataset in Colab by using Google Drive.
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Hi everyone!
I am studying timeseries generated by Google Trends for a number of search queries. They have different trends in different parts. I'd like to understand the point when the first significant trend started. In order to achieve that, I employed MK test with moving window, i.e. if the window equals 50, I take the first 50 elements of the sequence, apply MK test to them and write results to the 50th point; then move to the next points and repeat the test until the end of the timeseries. As a result, I get MK tests for all timeseries points starting from the end of the window and can detect when trends started to emerge.
The problem is that the results are hardly depend on the size of the window in a way that small window gives many short trends and large one have a time lag of trends beginning. Is there any easy way to understand which size of the window would be correct for a certain timeseries? I'm thinking about the use of standard deviation, but not sure how to correctly employ it and what is more important how to argument the its utilization.
Any help is highly appreciated!
Example of the data and MK test results are attached.
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Hi Konstatntin! Not really. I decided to calculate all possible windows for each endpoint and take median value of trend prob. The method is more or less workable and I believe may have interesting applications but so far with many crutches. So, I've decided to skip it for the current research. Maybe return to it later. If you're interested, I can share some py code related to the method application.
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I got AUC ( Area Under Curve ) of 0.3 during finding the sensitivity and specificity of a disease.
and I found in a google search there might be an error? so any idea how to solve this problem
regards
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Anton Vrdoljak thank you so much for the help
appreciate it
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Dear researchers,
Recently i have conducted a online survey work through google form.I want to know what could be it's methodology?
Help me suggesting any good articles where authors used/mentioned this types of survey process.
Thanks in advance!
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I agree with the previous thoughtful responses. I want to stress that as an alternative questionnaire instrument you may prefer the "Qualtrics.com" over Google form (It requires a subscription though). I found it is easy to get a better response since this platform provides a wider possibility of presenting your survey questions. Non-response rate might affect this kind of survey very much.
About the methodology, in addition to other ideal procedures in any other research, please consider some points:
-Develop your research question wisely based on a review of existing literature in line with the question of your interest
-If there is a control group, the characteristics should be commonly shared between the treatment and control groups.
-Close-ended questions are very helpful to reduce data management efforts after completing the data collection part.
-The selection of the study population needs to be validated in a systematic way for example who you choose to participate in the research. Questionnaires should be randomly distributed over any network.
I hope it helps.
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We've all been in circumstances when we couldn't find the literature we were looking for. Other times, we found exactly what we wanted, but very late. Thus, beginners in research are pushed to formulate a clear and innovative title. Keywords rescue us, but, is it enough?
In these days of data mining, what tools can we utilize to structure our research paper titles such that they are search engine optimized (SEO)? How can we write technical titles that are both engaging and readable?
1. Google Trends
Track changes in word usage over time, within a region, etc.
2. Web-of-Science
Regular keyword literature search, to find jargon usage.
3. Semrush
Helps with Keyword Research, Competitive Research, PR, etc. It is a marketing tool, perhaps used by industrial researchers and product developers?
4. What am I missing? What are your tricks and tips?
Thank you!
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Just use a simple description of your study, including your question, who performed the process, effects, and location . For example, my paper: 'Size-based fruit selection by a keystone avian frugivore and effects on seed viability in New Zealand' :)
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Everywhere import tensorflow_federated as tff this is being used but when I am writing this in google colab, it's not working. It's showing type error. What could be the problem?
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Hi all, I am depositing thin films onto quartz glass substrates, but due to supply problems the only adhesion metal available to me is chromium. My 2nd layer is silver to provide good conduction. Does anyone have experience with chromium-silver films? Does silver adhere well to chromium?
Done the usual googling and came up with nothing - maybe I'm not googling correctly.
Thanks in advance,
Nick
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I presume that you using silver layers for electrical conduction. Normally it is difficult to protect thin silver layers, as they oxidize very easily after some time.
Nevertheless you can use them for a quick experiment.
1) sputter clean thoroughly your quartz substrates in oxygen plasma at low rf powers (30 W) for about 10 minutes inside the chamber.
2) You should select an adhesion layer which alloys/sticks to your quartz (SiO2).
3) The adhesion layer and he top silver layer should be deposit insitu one after the another, with some substrate temper.
4) The adhesion layer (Cr, Ti or even Cu) should be very thin 20 to 30 nm, and should be deposited after achieving a good base vacuum. You can try copper, get a copper sheet and make a target out of it. Some substrate temperature is necessary for any of the adhesion layer Ti/Cr/Cu so that they stick well.
5) The deposit you silver layer immediate without breaking the vacuum.
6) Remember all depositions to be done insitu one after another, if you break the vacuum, then it may not work for such multi layered metallization systems.
There are excellent paper in literature, published many decades ago.
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I am trying to write a subroutine in Abaqus, in order to change the density of material after a specific strain.
like : Considering a simple tensile test, the density of every elements after a specific strain ( for ex: 0.1) decrease to half. it means the volume of each element should increase.
I did try VUMAT and VUSDFLD subroutines, however I didn’t get any results.
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In order to achieve this you need to define a material with tabular values of density vs field 1. In the Edit material increase the field variables to 1 and fill in the density vs Field 1 table. Then in the vusdfld you have to update the field values and the formulation in abaqus will handle the variation in density. The vusdfld should be something like that:
(*I haven't compiled or tested the subroutine, it is only for demonstration)
subroutine vusdfld(
c Read only variables -
1 nblock,nstatev, nfieldv, nprops, ndir, nshr,
2 jElem, kIntPt, kLayer, kSecPt,
3 stepTime, totalTime, dt, cmname,
4 coordMp, direct, T, charLength, props,
5 stateOld,
c Write only variables -
6 stateNew, field)
c
include 'vaba_param.inc'
c
dimension jElem(nblock), coordMp(nblock,*),
1 direct(nblock,3,3), T(nblock,3,3),
2 charLength(nblock), props(nprops),
3 stateOld(nblock,nstatev),
4 stateNew(nblock,nstatev),
5 field(nblock,nfieldv)
character*80 cmname
c
c Local arrays from vgetvrm are dimensioned to
c maximum block size (maxblk)
c
parameter( nrData=6 )
character*3 cData(maxblk*nrData)
dimension rData(maxblk*nrData), jData(maxblk*nrData)
jstatus = 1
c Collect strain values
call vgetvrm("LE", rData, jData, cData, jstatus)
c Update the field value with the strain value you need
call setField(nblock, nfieldv, nrData, rData, field)
return
end
subroutine setField(nblock, nfieldv, nrData, strain, field)
include 'vaba_param.inc'
dimension field(nblock, nfieldv), strain(nblock, nrData)
do k = 1, nblock
c For demonstration first strain component is used
strain11 = abs(strain(k,1))
field(k,1) = strain11
end do
return
end
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Hello. I imagine an online version of this test exists. But when I've tried to Google it, I get a load of stuff about the film Hidden Figures. Thank you. Gary
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Hello Every one,
My Google scholar account is public and not showing by google search. If any possible solution?
Here is the link
and also the snapshot is attached below.
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If I search for Dr. Imran Shah (so without "" and typing Google Scholar) it is the third page in Google.
Best regards.
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Hi everyone, I'm trying to understand if it is possible to show Abaqus results using two different contours for different parts at the same time. I tried to google it by I didn't find anything about it. Did anyone ever hear about this possibility?
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In the one viewport, we can have only one contour at a given time.
However, you can keep everything the same and create two different images with one contour at a time. Finally, mix these two images (in PowerPoint or other software) to show both contours in a single image.
Hope it helps.
Gopi
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What responsibilities are performed by the admin in a journal? Does the profile of an admin of a journal hidden from the outer world? There are some journals whose admin profiles are not found in Google search. What are the eligibilities required to become an admin?
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To answer your questions in order:
1. Responsibilities - to ensure manuscripts are in good order (and fulfil all the journal's) requirements prior to it being sent out to reviewers
When the manuscript comes back from the reviewers, they may had to convey it to the editor.
When it comes back from the editor (with a decision), they may have to convey it - positive or negative - to the author(s).
2. Hidden from the outer world? Yes and some of those workers like it that way so they are not seen and heard; some take the opposite and like to have a greater role
3. Eligibilities - none specific or common to all journals (I have seen some journals and the administrative assistant is very highly qualified!) but I generally agree with Biplab Kumar Chandra that being good with the language is very important to be successful in performing this role.
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I am working on a object recognition model that is able to detect whether the person in the picture is wearing any type of headwear or not (hat/cap/helmet/scarf/raincoat etc etc) . I am unable to find any large publicly available datasets of this kind. As of now I am resorting to writing scripts that scrape images from the web of people wearing hats/caps etc using bing image downloader API and Google image downloader API . Please let me know of any publicly available datasets of this kind. Thank you.
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Check this Dataset, could be useful:
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Is Google search engine the right place to get vital, genuine and reliable link or info?
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I am looking for a lecturer job for engineering college in India. Since there are millions of websites available on Google, most of them look like false advertisements or outdated ones. Here is my question: can some one please suggest me which website is more genuine based on your experience for finding lecturer jobs in India?
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Times Ascent, you can get latest updates on the related jobs in your region.
Employment News
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I have been struggling to obtain selectivity for weeks and is desperate for your help. It would be great if you guys can help me out with this. Save me :(
1. I have fitted the single-site Langmuir model. First question, do I use the 'q' value to proceed on the selectivity? The equations is
q=(qsat*b*p)/(1+bp)
2. I am trying to earn the selectivity in a gas composition of CO2:N2=15:85. When I apply the values to IAST selectivity equation, do I have to use the q(CO2) value at 0.15 p/p0 and q(N2) value at 0.85p/p0? Or q(CO2) and q(N2) at a same pressure for the equation below.
S=(q1/q2)/(p1/p2)
Someone please help me out. I am searching everywhere(i.e. google, youtube, papers) and cant find the answer.
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Hi,
The rationale you presented is not correct for IAST selectivity calculation. Two possibilities:
A) You calculate the selectivy from the Langmuir Equation, which is a constant and does not vary with the component pressures: S = (q1*b1)/(q2*b2)
B) You want to calculate IAST selectivities, which are not explicit and require iterations. The rationale for IAST calculations is presented in the chapter 5.3 in Do, D.D. (1998) Adsorption Analysis: Equilibria and Kinetics. Imperial College Press, London.
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Due unavailability of hardware i am performing my MD stimulation in google Col lab, so to escape the ideal time auto shutdown i split my 50ns stimulation into 5*10ns, now i have all the .trp, .xtc, .cpt.
for analysis step is it necessary to combine .trp, .xtc, files. if so how can i combine these files to obtain a complete 50ns stimulation file.
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...building on Magnus Bertelsen answer...
I think your best choice is to go with gmx convert-tpr. Just prepare a .tpr file which is 10ns of simulation time. Once this is completed, extend the time of the simulation with
gmx convert-tpr -s your_old_tpr_0to10ns.tpr -o your_new_tpr_10to20ns.tpr -extend 10000
Then run the simulation by starting from the old checkpoint file of your 10ns sims, something like
gmx mdrun -..[various flags] -cpi old_sim_0to10ns_checkpoint.cpt
This will build on your previous generated files and the new data will be appended on the files that you have from the first 10 ns of sim. In this way you will end up with only one .xtc/.tpr/.edr/etc file at the end of the 50ns, that is, after you repeated this extending procedure 4 times.
Eventually, if this is not permitted by the service you are using, you could add the -noappend flag to mdrun to keep the files divided. Give it a try before relying on trjcat.
Best
Nicola
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For a research project, I want to replicate the analysis of Li et. al. (2015) for a different city
I can read that Google changed their Terms of Service (https://cloud.google.com/maps-platform/terms) since the publication of the article. Some of the elements related to this study are:
3.2.3 Restrictions Against Misusing the Services.
(a)  No Scraping. Customer will not export, extract, or otherwise scrape Google Maps Content for use outside the Services. For example, Customer will not: (i) pre-fetch, index, store, reshare, or rehost Google Maps Content outside the services; (ii) bulk download Google Maps tiles, Street View images, geocodes, directions, distance matrix results, roads information, places information, elevation values, and time zone details; (iii) copy and save business names, addresses, or user reviews; or (iv) use Google Maps Content with text-to-speech services.
c) No Creating Content From Google Maps Content. Customer will not create content based on Google Maps Content. For example, Customer will not: (i) trace or digitize roadways, building outlines, utility posts, or electrical lines from the Maps JavaScript API Satellite base map type; (ii) create 3D building models from 45° Imagery from Maps JavaScript API; (iii) build terrain models based on elevation values from the Elevation API; (iv) use latitude/longitude values from the Places API as an input for point-in-polygon analysis; (v) construct an index of tree locations within a city from Street View imagery; or (vi) convert text-based driving times into synthesized speech results.
My question is thus: Is it still allowed to perform this type of research? Or is there another way that this type of research can be performed without the use of Google Street View?
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I believe so, in some articles there is a concern to discuss vegetation not only by the horizontal notion, but also by the vertical vision, and in this aspect, Google Street View presents itself as a very useful tool. Always remembering that it must be in accordance with the objectives of the work.
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For my thesis I need to estimate BEKK GARCH models. For this I have tried several packages. I keep getting the same error: "H is singular" or "in sqrt(diag(Hessian))): NaN produces". I have found that this can be caused by highly correlated series, or series very close to zero.
To make sure it had nothing to do with my data (I am modeling cryptocurrencies and other asset classes), I tried to run the BEKK model on different series. I have tried to run in on Google, IBM, microsoft, GOLD index and other series, but I keep getting this error.
One example of code I have tried where I got this error is:
getSymbols("MSFT", from = startDate, to = endDate)
getSymbols("GOOG", from = startDate, to = endDate)
data <- data.frame(dailyReturn(MSFT), dailyReturn(IBM))
log_returns1 <- diff(log(MSFT$MSFT.Adjusted), lag=1)
log_returns2 <- diff(log(GOOG$GOOG.Adjusted), lag=1)
log_ret <- merge(log_returns1[-1,], log_returns2[-1,])
estimate <- BEKK(log_ret, order = c(1, 1), params = NULL, fixed = NULL, method = "BFGS", verbose = T)
I still obtain parameters but the results cannot be right. I get totally different parameter estimates with different packages. Also, when plotting the dynamic correlation obtained from the model it looks more like a return series that bounces between -1 and +1.
I did get "Valid" parameters for the BTC-VIX series using the MTS BEKK package, namely no significant volatility spillover. But even here the dynamic correlation obtained from the model was not correct.
Edit:
I have simulated BEKK GARCH data using rmgarchBEKK package and used the simulated data to estimate the BEKK GARCH model, but I still get the: "H is singular" and "negative inverted hessian matrix element" error. Even when using the same package that I used to simulate the data with.
Code:
simulated = simulateBEKK(2, 1000, c(1,1))
simulated <- do.call(cbind, simulated$eps)
testEst <- BEKK(simulated, order = c(1, 1), params = NULL, fixed = NULL, method = "BFGS", verbose = T)
I have used: MTS and mGARCH-BEKK package, with both packages I get this error.
Any help would be greatly appreciated.
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Had the same issues. Therefore, I would like to recommend the newly developed Package "BEKKs" to address them:
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I have a question. I wish to analyze the career interest of my students for Pharma Industry, Cosmetic industry, and Chemical Industry. I have created 10 multiple choice questions for area. I want to offer these on google forms where 30 questions are shuffled (not in order for each industry). But at the end I want the students to see the score for each of the domain i.e. pharma, cosmetics, and chemical. Is there a way to do that? Can I also add comment for eg. Based on your score you are most suited for pharma etc.
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On what basis did you assume questions would show suitability? How will you validate?
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Hey guys,
I am currently doing a research and I got confused with the statistical methods. I googled for some infos but wasn't clear exactly which method i should use.
So, my experiment is a within-subject design. There are two conditions and subjects participate in both of them. Plus each condition has two trials. (So there are two conditions and four trials in total.)
I wanted to see whether there is a difference in subjects response between the two conditions. At first, I was considering RM ANOVA but the dependent variable is dichotomous so it won't work. Then I found that General Linear Mixed Model or McNemar test might be the alternative options but I am not sure.
Plus I might later consider participant's age as a between subject factor.
Any advice or help will be really helpful.
Thanks!
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Hello Jisoo Oh . Here is a blog post you may find helpful. I've also given a link to the article the blogger recommends--To GEE or not to GEE! HTH.
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In my research work ,I need super computer to use gaussian 09 in simulation , I want to use google cloud for that .
So ,how can use google cloud in simulated by gaussian 09?
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UberCloud
TheUberCloud
If you're an IT leader supporting engineers, you have a challenging task keeping up with the latest advances in cloud technologies.
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