Suggestions for citation plugin/add-on for Linux Office Suites?

Hello,

are you able to advise me as to the necessary steps to publish my dissertation, which covers CTCA utility in older adults.

Many thanks

Janet

When installing Gromacs 5.1.5 in Ubuntu v22.04, I receive several errors. I have attached the error files.

I am currently creating a species distribution model with Maxent in R. The problem I am facing is that the habitat suitability prediction is always different. When I run the model twice, with the same configuration, two different maps will result. That is because I use random background points (there is no sample bias in my data, so no need for that) and these are of course always randomly sampled.

So how should I treat that. Should I create ten maps and average the habitat suitability value? Or should I evaluate the model each time and choose the one with the highest evaluation metric score?

If someone has literature on that would be good as well.

Hi, I am not able to install the GROMACS 2021 version on my Linux machine based on ubuntu distribution. If someone guides me then its would be help full. Here is the screenshot of my machine, installed Cuda cores on NVIDIA GPU.

Thanks in Advance.

What is taxonomy? what is not? what does it do? what doesn't it do? What would happen to humanity without taxonomy? what changes? How can taxonomy, as a basic science, gain the importance it deserves, especially in scientific and daily media sources, and how can it be brought into the focus of attention again? Why are auxiliary sciences receiving more attention? etc...

Hello Researchers,

I mostly use WPS and Libreoffice but the problem which is face several times is addinf references and citations. Because even when we change one of the reference it doesn't get updated in the text of research article.

I just checked ENDNote but thats not comaptible with LINUX. So someone who is using such tools or tricks in WPS or Libreoffice , kindly please update me.

Thanks,

Abhinav Nag

Which is the difference between both buffer? I used to use buffer with SO4, but suddenly my PCR started give me problems, any sign. So I changed the buffer for a buffer with KCl, and my PCR worked well. Someone can explain me please?

Hello everyone,

Lately I am having trouble with PCR of my DNA samples. I keep on getting a band in my negative control. My targeting region is very small (190 bp) on the 18S mtDNA. This band is slightly smaller or the same length. Primer clouds are also visible at the very end. I first thought of contamination, that is why I changed everything, pipetting tips, reagents, tubes, cleaning with bleach, but still a band. Two strange things rising up, it worked in the very beginning, also the blocking primer which does not seem to work properly the last PCR times. Plus if I add water as DNA template or the buffer used for the DNA extraction, the band shows up, but if I only use the mastermix for the PCR, there is no product at all visible in the gel.

PCR is running at 35 cycles, which is a high amount, but it used to work before and anneling temperature was set higher already. I am kind of desperate, maybe anyone does have a good suggestion what I might can try to solve this problem.

In any case I would be happy about some help!

Thanks in advance.

Hello, I have complete and ready research papers in communications engineering, computers or information technologies, and I need authors to enter with me to pay the publishing fees in Scopus or Clarivate Journals . Anyone interested writes to me