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Recent Replies
Comment: Bwa sampe - BGI
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Honestly, use bwa mem like everyone else and call it a day.
bwa mem ref.fa X1.fq.gz X_2.fq.gz | samtools sort -o sorted.bam
See the b…
Comment: Bwa sampe - BGI
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lorena9132
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Hello, thank you very much for your response. I was referring more to using these options:
-a INT Maximum insert size for a read pair …
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Take a look at [this post][1] ... it might give a clue.
Alternatively, for my installation the qcmodule is located at:
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The [biostars handbook][1] is well worth the money
[1]: https://www.biostarhandbook.com/
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Thank you @atpoint for your reply, but I think I didn't explain myself clearly. Initially, I compared my two datasets to their control and …
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Most advise to avoid For Loops in R (don't ask me why, unexpected results and behaviours, poor efficiency I think). I would use tidyverse f…
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P-values are not corrected for the multiple comparisons inherent in differential gene expression analysis. FDR (aka qvalue) is used for sel…
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Hi, im traying to do something similar, could you share the code to do what you describe.
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Colin's answer is essentially the right one I believe, but the more immediate consideration is: *what are you actually trying to show?*
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https://www.biostars.org/p/9554614/ ; <br>
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https://www.biostars.org/p/9583727/ :<br>
https://www.b…
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bwa sampe produces unsorted SAM , not BAM.
converting SAM to BAM will reduce the size
sorting the BAM will reduce the size (you can …
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Hi! Should I delete the stack exchange post? I didn't know that cross posting is bad.
[https://meta.stackoverflow.com/a/425789/5140632][1]
…
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You need a genome browser and you can probably use GBK or gff3 format.
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cross-posted https://bioinformatics.stackexchange.com/questions/22401
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