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Returning gene functional annotations with gene symbols as input (using mygene Bioconductor package)
written 2.4 years ago by
Bohdan Khomtchouk • 320
• updated
2.4 years ago by
EagleEye ♦ 6.5k
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written 4.6 years ago by
pankajnarula84 • 10
• updated
3.3 years ago by
EagleEye ♦ 6.5k
4
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Recent Votes
- A: There is some way to split a FastQ file by chromosome?
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- C: There is some way to split a FastQ file by chromosome?
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Recent Replies
-
C: There is some way to split a FastQ file by chromosome? by
calebe_campos26 • 0
At the first moment, I was right that the file type from SRA was FastQ, but I read in some tutori...
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C: There is some way to split a FastQ file by chromosome? by
calebe_campos26 • 0
I'm using a software (a site, to be more specific) called RepeatExplorer and the input file requi...
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C: Volcano plot for multiple clusters by
michelle.piquet • 10
How do I go about merging the results table since all the p values and log fold change values are...
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A: There is some way to split a FastQ file by chromosome? by
swbarnes2 ♦ 7.0k
> Convert the FastA to FastQ, A fastq contains more information than a fasta. You can't "con...
-
A: Criteria for merging multiple VCF files by
Brice Sarver • 3.2k
If you're combining non-filtered VCFs, it would make sense to expect a lot of false positive vari...
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C: Map gene presence/absence (i.e. gain, loss, duplication) on phylogenetic tree by
djamalova.d • 10
Thank you for your response. I have a species tree and output file from ProteinOrtho5. I convert...
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C: There is some way to split a FastQ file by chromosome? by
genomax ♦ 75k
> I need the FastQ file of each bovine (Bos taurus taurus) chromosome. Can you tell us why? A...
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C: Trimmomatic Error (Exception in thread "main" java) by
genomax ♦ 75k
You need to have `-phred33` and not bare word like you have in your command line.
-
C: There is some way to split a FastQ file by chromosome? by
Joe ♦ 15k
1 - You can't convert FASTA to FASTQ. They don't contain the same information. 2 - If you downlo...
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C: Which counts to use for RNA-seq heatmap and PCA? by
Lucy • 40
`heatmap.2(tmm_log, trace = "none", col = bluered(20), scale = "row")`
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julien.fouret.fr • 20
I have always used QUAST but without bam Nothing is wrong about your bam and if you're using ana...
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C: Analysing BAM files by
julien.fouret.fr • 20
Yes. In my point of view, If this 5 varieties are very similar, the simpliest would be to avoid...
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