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written 2.1 years ago by
Whetting • 1.5k
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uzmaabdulsalam • 0
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written 10 months ago by
ricfoz • 20
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10 months ago by
Kevin Blighe ♦ 39k
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written 10 months ago by
victoria_aleks • 30
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10 months ago by
h.mon ♦ 24k
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written 12 months ago by
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written 4.0 years ago by
confusedious • 420
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2.3 years ago by
Biostar ♦♦ 20
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written 4.9 years ago by
pld ♦ 4.8k
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3.1 years ago by
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written 3.2 years ago by
cryomics • 0
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3.2 years ago by
Michael Dondrup ♦ 45k
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written 3.9 years ago by
Adrian Pelin • 2.2k
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3.9 years ago by
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The difference between posterior probability value and Clade credibility values generated by MrBayes
written 4.0 years ago by
YMTIO • 0
7
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2
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6.6k
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6 follow
2
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written 5.6 years ago by
kanwalashraf07 • 30
• updated
4.3 years ago by
Michael Dondrup ♦ 45k
10
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written 4.9 years ago by
Adrian Pelin • 2.2k
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4.3 years ago by
Michael Dondrup ♦ 45k
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1.1k
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written 4.3 years ago by
Ginsea Chen • 120
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4.3 years ago by
5heikki ♦ 8.2k
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1
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written 4.4 years ago by
Ginsea Chen • 120
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4.4 years ago by
Brice Sarver • 2.5k
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written 4.5 years ago by
Ginsea Chen • 120
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4.4 years ago by
Biostar ♦♦ 20
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written 4.5 years ago by
Ginsea Chen • 120
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4.5 years ago by
Devon Ryan ♦ 88k
3
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Tool:
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written 4.5 years ago by
bagdevi.mishra • 50
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4.5 years ago by
Istvan Albert ♦♦ 79k
1
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3.5k
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1
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written 4.9 years ago by
Adrian Pelin • 2.2k
• updated
4.9 years ago by
David W ♦ 4.7k
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Recent Replies
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C: An error message while installing gromacs on windows 10 (Linux bash shell, ubunt by
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Thank you for your answer. I successfully installed but I couldn't execute it. Could you hel...
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Cool. The model may then simply be `~ PatientID + treatment`. This model is then effectively a pa...
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I noticed that before, but not with RNAseq. It was a kind of artificial set up, where the sequen...
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Thanks for your answer, I will try anaconda.
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This gene has [multiple transcripts][1] and Uniprot seems to assign them with unique ID's. @Emi...
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Check this link if you want to merge multiple vcf files https://reneshbedre.github.io/blog/mergev...
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Check this link to merge vcf files https://reneshbedre.github.io/blog/mergevcf.html
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If you do a google image search with `fastqc per base sequence content` you will see examples of ...
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Here's one approach. It's a little hacky, and going back to the original sequence to find the ind...
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C: How to analyze RNAseq data with two/multiple treatment groups and each subject h by
wwu222 • 0
Hi Kevin, really appreciate your suggestion! I will try it out. Thank you very much!
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C: Converting a VCF with SNPs and indels to BED format by
jeb247 • 10
Please try removing the leading "$" from: $ cut -f1-5 foo_snvs.bed | awk -v FS="\t" -v OFS=...
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Yes - I believe the rlog is mostly similar to log2(FPKM+0.1) values. So, it is more like the log...
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