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cristina.dellabeffa • 0
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4.3 years ago by
GenoMax ♦ 96k
Recent Votes
- Why may BOLT-LMM and SAIGE (quantitative, linear-mixed model) yield different results when ran on the absolutely the same dataset?
- Why may BOLT-LMM and SAIGE (quantitative, linear-mixed model) yield different results when ran on the absolutely the same dataset?
- Help with Mr Bayes parameters for 16S phylogeny
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Recent Replies
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C: FastQC per base to total base calculator by
GenoMax ♦ 96k
FastQC produces a companion zip archive that should contain all the data used for generating Fast...
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A: bcftools command not working by
GenoMax ♦ 96k
Most likely. Power9 CPU's are not compatible with x86 binary that you likely downloaded. You will...
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GenoMax ♦ 96k
Did you verify that `esearch` is bringing back valid results for all queries? For many accessions...
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A: How do I use FindAllMarkers after making additional cluster assignments? by
Pancreas Pratik • 110
So this was solved with the help of @nbpeterson3 on the Seurat github Discussion page. So when F...
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A: finding bacterial genes in dataset by
john.chandler2011 • 0
Thanks, I will check it out.
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You can just copy ENA fastq ftp links and downloaded them with `curl` or `wget` directly to the s...
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mfshiller • 10
That's actually one of the solutions I thought about. Either: 1. increasing sample size 2. corre...
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Mensur Dlakic • 9.0k
It would be very difficulty to see individual proteins and their interactions when the number is ...
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Ram ♦ 32k
Please see https://www.biostars.org/p/309884/ to add your images properly. You need **the direct ...
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C: Very small quantity of adapter contamination, real or not? by
GenoMax ♦ 96k
If you are going to use `stacks` then that should work.
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Hi, I have two similar DEG lists, one worked very well with pathfindR, but the 2nd one failed ...
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gamamiguelangel • 0
Maybe this paper will help you :) >Terminating contamination: large-scale search identifies mo...
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