Questions related to Program
For those who wish to learn!!!! After the first successful Symposium Square Bamboos and the Geometree, we now announce the Second Symposium on 4 and 5 December 2023. It is fully online. The contributions span a wide range of subjects, but the common themes are: 1) Cutting edge research on Form and Shape in Geometry and in the Natural Sciences, and 2) Transcending Boundaries This year we have another exciting program with lots of geometry, with close connection to biology and physics.
I'm currently trying to find an rRNA promoter in Kingella kingae. While looking for a good analysis program, I found out that the most widely used ones (Genomatix, BacPP, MEME etc.) either don't seem to be functional or the site can't be reached. I also tried SAPPHIRE, which kept finding -10 positions with sequences not even present and the only site which gave somewhat credible results was Bprom. Even though, it suggests that the -35 box is longer than the -10 one, is that a possible outcome?
Can anyone please suggest a good program with a functional url, preferably a free one? And if you have experience with promoter analysis, would you be so kind to give me some tips on what to look out for? As a student with no experience with promoter work, it seems pretty confusing to me, moreso in a bacteria with a relatively unannotated genome with almost no papers on conserved promoter sequences.
Thanks in advance!
I've been using Photoquad software to analyze photoquadrats but suddenly the program doesn't run anymore and I am not able to solve the problem. I uninstalled both the MATLAB Compiler Runtime (MCR) and Photoquad.exe, reinstalled everything being careful to follow all the installation instructions and suggestions by the manual and the web (https://www.mar.aegean.gr/sonarlab/photoquad/), I freed up space on the hard disk, among other actions, for possible problems not related with the software itself, I respected all the times the program takes to run, etcetc.... but it's impossible to make Photoquad runs neither to open the main window.
I don't find the solution and I really need to continue my analysis. Anybody had the same problem or may provide any suggestion in order to fix it?
Thanks in advance for your help!
Dear professor, I would like to know how the overturning curve is drawn in the study of rigid block swing overturning, and can you send some programs to help me understand more deeply, thank you！
I will begin my dissertation research in January 2023. I would like to determine if ResearchGate is a suitable platform for recruiting participants for my survey.
I would like to inquire if there are current or former principal investigators, co-investigators, and program directors/managers who have, either currently or in the past, been recipients of federal awards for biomedical research who would you take a 15-minute survey to support my research. If not, could you kindly share your reasons?
health education program covering stress, depression, anxiety, and positive coping strategies, that can use intervention to improve mental health among adolescent ?
In the ongoing project focusing on the design of a Prosthetic Heart and Venous Valve, our objective is to enhance the optimization of the materials used. Our focus is to prioritize materials with the highest level of durability. Following the acquisition of secondary values from the samples tested in the controlled environment, we will process this data digitally and conduct comprehensive fatigue analyses of the entire structure. In this fatigue analysis, our intention is to introduce the load as a cycle with variable amplitudes. While the ANSYS Mechanical program allows for variable amplitude definition, it restricts the load to a single surface, which is not in line with our preferred approach. Moreover, the ABAQUS Fe-safe program does not permit variable amplitude definition. We are thus inquiring whether any prior research has been conducted on a similar scale, yielding accurate results. Is such an analysis possible?
"For a mixed-integer linear programming model M with feasible solutions, by taking the non-zero valued variables from the linear relaxation solution of model M to construct the solution space of model M, is the integer programming model M guaranteed to have feasible solutions?"
What is the appropriate academic department for the occupational health and safety program and what are the justifications for that?
Is establishing this program under the Department of Clinical Nutrition acceptable and appropriate, and how does this affect the career and professional and competition between those who graduated from the same program but under the Department Public Health or under the Department of Environmental Health?
I have converted the raster to points in the GIS software and transferred table attributes to the Origin Pro program through an Excel file to draw a diagram. But there is a problem with it that I don't know which part it is from. Also, I encounter many errors in the Origin program, and only one graph is drawn from it. Can you please guide me regarding this problem by classifying the points? I have attached some Documents for a better understanding of the information.
Dear Research Community,
As a newcomer to the field of research, I am seeking guidance on a specific matter related to affiliations in research papers. Consider a scenario where a student is currently enrolled in an online Master's degree program at a reputable institution, such as the University of Berkeley. This student is preparing to publish a research paper in a peer-reviewed journal.
My question pertains to the formatting of the "affiliation" section. Should it be presented as follows:
Emma Smith Department of Engineering Management University of Berkeley, Berkeley Masters Of Engineering in Engineering Management Email: firstname.lastname@example.org
Or would it be more appropriate to include the term "Online," like this:
Emma Smith Department of Engineering Management University of Berkeley, Berkeley Masters Of Engineering in Engineering Management, Online
Should I make it more specific to write it in affiliation section as a online program
I appreciate your valuable insights and expertise on this matter
I have used the antiSMASH program to derive the biosynthetic gene cluster (BGC) from bacterial genome. At present, I want to use BiG-SLiCE program to cluster the homologous BGCs into Gene Cluster Families (GCFs). I would like to know the format of the input file required to analyze the BGCS in BiG-SLiCE program?
There is syntax error in the math section of "sdevice" in TCAD, and as a result, the program cannot be executed.
It seems like an error has started occurring suddenly, starting from the "Extrapolate" section. While you made some structural changes to the component, it didn't affect other modifications. You've considered adding the "Quasis" section to the solved section based on your research, but there seems to be inconsistency compared to the previous behavior.
Where could the issue be coming from?
I am working with Gaussian 16 program package. For one of my geometry optimization calculations more than 100 geometry cycles runs are required. But even when I am including the tag "opt=(maxcycles=150)" in the input, it runs only up to 100 geometry cycles. So, please suggest the ways to increase the number of geometry cycle runs.
Your suggestions would be appreciated.
I have to use a magnifying glass to read the display on a lot of the parts of the program, how can I change the fonts into something readable? I already tried changing Windows Settings->All in One Fonts & Icon Size to the large setting, it only changes some of the fonts.
Makes the program really hard to work with if I cant see any of the commands because they are too miniscule
I want to make a path model on Lisrel 8.80 but when I run the model it said my model does not converge and there is a warning that says W_A_R_N_I_N_G: PHI is not positive definite and W_A_R_N_I_N_G: The solution was found non-admissible after 50 iterations.
My model as following:
Raw Data from file 'C:\TA\hgkghk.psf'
Sample Size = 151
Latent Variables T RL RP A E SAT LOY
X11 X12 X13 X14=T
X21 X22 X23 X24 X25 X26 X27=RL
X31 X32 X33 X34 X35 X36 X37=RP
X41 X42 X43 X44 X45 X46=A
X51 X52 X53 X54 X55 X56 X57 X58 X59=E
Y11 Y12 Y13 Y14 Y15=SAT
Y21 Y22 Y23=LOY
End of Problem
I tried the preliminary solution by writing ADMISSIBILITY OFF before end program but it didn't fix the problem. How do I fix my problem?
Thank you so much for your help.
Hello, everyone. I am Xing Ning.
I find in my Matlab program, when the location (x,y) is near the boundaries between two different regions, the analytical waveforms of Bx and By exist fluctuations. If y value of Path 1 of Region1 is 0.0995m, the analytical waveforms of Bx and By is calculated as shown in Attached file.
I can ensure that the parameters of matrixes are defined and calculated correctly. I can't figure the errors out.
Thank you for your time and effort.
Ning Xing, China
any body can share the most suitable question need to ask about the impact of certain program (eg. Islamic medication)on daily life?
I'm in the final year of my MPhil program in Education and I'm on the lookout for potential Ph.D. positions at universities in Canada. Specifically, I'm interested in the realm of "Educational Leadership and Management." I'm wondering if there's an efficient way to identify suitable supervisors at institutions like the Ontario Institute for Studies in Education, or other Canadian universities, who share this specific research focus. Going through each supervisor's research individually is proving to be quite time-intensive. Your insights would be greatly appreciated.
Thank you in advance.
I have my XPS data quantification, I gonna make a graphene oxide model using the quantification data, do you know which program I can use?
I am capturing fluorescent microscopy images of a developmental process with a high degree of variability. I need to compile these images into a "gallery" so that I can see many/all images at once to look for possible phenotypic differences between conditions, which then I can measure through FIJI. The most basic way I can do this is by arranging the images in a Powerpoint, but this method feels manual and has some limitations (explained below). I am hoping someone may know of a better way to compile image data for investigation/curation, maybe through FIJI, R, or a different dedicated program.
Limitations of Powerpoint:
1. Cannot track sample group or ID: When you upload an image into Powerpoint, there is no way to check its filename. So I am forced to upload one image at a time (and make a text box noting condition and ID), which is slow and unideal for batch processing images.
2. Re-formatting and arranging is manual: Re-sizing, cropping, and positioning images on Powerpoint is very manual and there is no record of changes (so making scale bars is hard). The effort compounded when the need arises to re-size or re-position the images later in the process (see #3).
3. Cannot re-order images dynamically based on values: Because the process I am studying is highly variable, it is necessary to compare images at the same percentile between conditions. Thus, I would like to re-order the images by measured values (so that I can compare min to min, mid to mid, max to max, etc.). This is also useful for selecting representative images for presentations/papers.
4. Interactive/Shiny Graph: To further aid in comparing images based on values, it would be nice to have an interactive/shiny scatterplot of the measured values such that when you hover over/select an image the corresponding datapoint in marked in the graph.
A. Keynote: Solves #1 because uploaded images retain the filename information. However, the file format is limited to Macs which limits data sharing.
B. QuickFigures: This FIJI plugin solves #1 and #2, but it is still clunky to use and cannot re-order images.
C. Image Data Explorer: This R package or browser program solves #4 but can only view one image at a time. It also has the advantage of easy annotation of the images by entering values into the corresponding data spreadsheet/dataframe.
Does anyone know of a way/program that solves any of these limitations? Or does anyone have a different way of compiling image data?
I need guidance on the different steps taken when starting up a mentorship program in the organisation and what are the necessary documents that I need?
I cannot introduce the name of this Journal Revista Democracia digital e Governo eletrônico where I have published my article. The program does not function correctly. The Revista has the ISSN: 2175-9391. Why?
How can I calculate the SOMO value to be able to perform SOMO-HOMO calculations? When I do the HOMO LUMO calculations of the structure I'm working on (spin doublet), I see two values due to the spin state. What is required for me to do this work?
Dear colleagues - i am working with temporal bone histology prepared in celloidin. The slices are about 20 microns thick and were stained with H&E. The material was digitized and saved both in JPG and Raw formats. I am looking for a program that can do 3D reconstructions, preferably straight from the histology images (meaning no need to pre-delineate the areas of interest). Does anyone have any program recommendation or experience with this type of work? Appreciate your comments! Thanks! Miriam
Hello everyone. Could someone please tell me how or where I can get the following Excel spreadsheet programs:
1) (FC–AFC–FCA and mixing modeler: A Microsofts Excel & spreadsheet program for geochemical modeling, of Yalcın Ersoy, Cahit Helvacı).
2) (AFC-Modeler: a Microsoft® Excel© workbook program for modelling, of Mehmet KESKİN).
3) (PETROMODELER (Petrological Modeler): a Microsoft® Excel© spreadsheet program for modeling melting, of Emrah Yalçın ERSOY).
I will really appreciate any help, thanks.
In the MATLAB language, when using the FCM algorithm, we find that it deals with some default options, for example, it uses the Euclidean distance, and when we want to use another type of distance, the program refuses to execute. Is it possible to modify these options?
What makes an effective teacher education program is a question commonly asked by educators. In your opinion, what are the indicators of an effective teacher education program?
I have been using dedoose which is a monthly online subscription.
I'm satisfied but find it very costly and now sort of 'golden wshackledled' since my data and coding are there. I'd like to consider purchasinga one-timeime program, that still would enable more than one person to work simultaneously on the same data set. - a good feature of dedoose.
I'd be grateful to learn others experience with varied program.
for an analysis, I would like to create a pretty Forest Plot. However, it would be important that one can play with the scale of the x-axis, e.g. the first 2cm are in 0.1% steps, the next 2cm in 1% steps and the last 2cm in 10% steps. Does anyone here have a recommendation for a program for me that would be capable of this?
Thank you so much for any suggestions!
I am seeking assistance on ResearchGate for debugging a Fortran program using gdb. The program consists of multiple subroutines written in different modules. Whenever I attempt to step into one of the subroutines to examine the underlying calculations, gdb encounters the following error: "Thread 1 hit Breakpoint 1, hardening::hardmodel10 (iphase=1, nslip=12, temp=298, dtime=0.0099999997764825821, g12=79800, burgerv=..., totgammasum=8.3999999999999995e-05, gammadot=..., pdot=0, gammadot_slip=..., gammadot_climb=..., absrss=..., signrss=..., rss=..., nidot_climb=..., didot_climb=..., climbmodel=1, climbparam=..., hardeningmodel=1, hardeningparam=..., hintmat1=..., hintmat2=..., tauc_t=..., loop_t=..., rhomobile_t=..., rhoimmobile_t=..., rhototal_t=..., ni_t=..., di_t=..., drhomobile=..., drhoimmobile=..., dni=..., ddi=..., dloop=...) at ../UMAT/hardening.f:795" The following error message is displayed: "../../gdb-10.2/gdb/gdbtypes.h:527: internal-error: LONGEST dynamic_prop::const_val() const: Assertion `m_kind == PROP_CONST' failed. A problem internal to GDB has been detected, further debugging may prove unreliable. Quit this debugging session? (y or n) [answered Y; input not from terminal] ../../gdb-10.2/gdb/gdbtypes.h:527: internal-error: LONGEST dynamic_prop::const_val() const: Assertion `m_kind == PROP_CONST' failed. A problem internal to GDB has been detected, further debugging may prove unreliable. Create a core file of GDB? (y or n) [answered Y; input not from terminal]." I would greatly appreciate any assistance in resolving this issue.
We need a new program for statistical analysis that provides results different from what is provided by the usual programs in the analysis
- I want to make a unit cell of NiO. We know that NiO is an antiferromagnetic material meaning the magnetic moments of the neighbouring Ni ions align in an alternating manner (one spin up and then down). So what should be the coordinates of the Ni and O ions, so that if I want to make a unit cell/supercell, the program can understand the location of spin up and down of Ni and the non-magnetic ion O?
I hope to bring more robust HAES programing to the local community college in Washtenaw County and community. Is anyone aware of resources for health behavior and education programing on HAES? I am specifically looking for curriculum and programing for short term (anywhere 4-12 weeks) focused on behavioral health in informal group setting, with measurable outcomes. Programing could include for example marketing materials, guided session materials, reference books, recommended timeline of program and activities, book review questions, and references to pre-existing HAES programing (both online and inperson) for more indepth coaching/programing.
I have been unable to find anything of the sort, and would appreciate the insight. If this is not something that exists, I would endeavor to create such programming with like-minded and skilled public health or medical professionals. Please DM me if you are interested.
I prepared a 23-page article on parameterization. I submitted the article to a journal known as "good" in its field. After keeping my article for 4 months, the journal suggested a revision. Although the proposed revision appeared to be "major", it was actually a "minor" change due to the reviewers' lack of knowledge about the subject. The reviewers were asking for impossible changes about a subject they did not know (they asked why I didn't write my program in C++ which I wrote in Python, why I didn't use FTIR calculation in parameterization, etc.) and neither of them had any command of the subject of "parameterization". I made my explanations and 6 months later I got a rejection for a ridiculous reason that I "did not respond to the referee's questions" ( I responded with 17 pages and the email they sent after my responses had nothing to do with my responses; these two referees who wanted to present themselves as proficient in the subject ignored my responses like two fraudsters and played various word games: For example, they alleged that my program would not work without the Antechamber program used in the molecular dynamics procedure, and asked why I didn't publish it in the AMBER package, whereas that process was not related to my program, it was already part of the molecular dynamics procedure. They alleged that the VFFDT program would automatically number, I copied that part from the manual and wrote that it can't do it, if it can, show how it is done, they didn't respond to that either :) The other referee first said that the formula I took from the AMBER Manual was wrong, look, he said it was wrong, he didn't say the formula was incomplete or erroneous, he said it was wrong. In the reason for rejection, he found an excuse like "why did you write the formula in a way that will confuse the reader" since he understood that it was not wrong. You would appreciate that I had to hold myself not to swear.) ..and I got rejected. I was very surprised that a journal with such a good impact factor appointed two ignorant referees who really did not know the subject, did not understand the subject but insisted on pretending to understand the subject. The journal appears to be famous in its field and we corresponded occasionally with the editor-in-chief during the article process, actually the editor-in-chief is quite proficient in the subject and would never make the comments made by these two fake referees. Either due to bad luck or the incompetence of the field editor, I lost 6 months. Therefore, I want to learn the names of these two reviewers and write their names as "opposing referees" in my next articles. Do you think doing this would create an ethical problem? Since the incident happened to me, I could not make an unbiased decision. Therefore, I wanted it to be discussed here before sending the email: What would you do if you were I? Thank you.
My company is looking to design a L&D program for Employee Skills Identification. We are looking to use BCI technology for the same and it would be of great help if we can find an SME with whom we can collaborate to conduct this.
Hello, I'm trying to calibrate a material I tested in real life for Abaqus, but the program keeps displaying the error whatever I do. I even converted the stress-strsin curve from engineering to true stress/strain but it didn't solve the problem. Please help!
I try to do match with some compounds but I could not find the JCPDS No. 03-065-3419 and 0-065-0395, in Xpert program
can you help me plz
I'm currently in the analysis phase for a program evaluation/scale development project where most of the questions follow a standardized option response format:
Neither agree nor disagree
However, there is one item whose response options are:
My question is, for the type of analysis I'm doing (year over year differences, some validity/reliability using R), would this item for which the mid-point response option is "Neutral" as opposed to Neither agree nor disagree" make a significant difference in my analysis results? Could I interpret the results with confidence given the change in wording for the mid-point option, or could I move forward with analysis with the inclusion of this item? I would omit it entirely, but it belongs to a scale comprising 5 items.
Thank you in advance for any guidance!
Do you design software when you “write” a program? What makes software design different from coding?
If a software design is not a program (and it isn’t), then what is it?
Is software in different places programmed in different languages? What are some of the regional differences in computer systems and programs?
How are these related to different networks like .com, .net, .in?
For example, are people programming using Java in different langauges or in English, or are other programming approaches used?
Do people use different encryptions to isolate their systems, or do they use different networks, or different regional software altogether?
I'm a 2nd yr intern.
I have been tasked to reproduce a graph(Fig. 4) from a paper(linked below). I have tried for days still I have no idea how to program the TSC network model as i haven't had any course remotely related to ti and also there's nothing helpful i could find on the internet. I'm honestly lost.
Would be a real help if anyone can throw some light on it.