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so which one should i prefer? i don't need the entire results i need the condition-Germline table only. (for eg:-from, https://www.ncbi.nlm…
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OK, not sure why your intention is to use RSEM p-values for, but at least tell us the commands you ran then otherwise how are we supposed t…
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> Don't forget to follow up on your threads. If an answer was helpful, you should upvote it; if the answer resolved your question, you shou…
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Sure, I'll inquire about the version of Rsubread. I'll keep you posted if it works :) Thanks
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Yeah, let me show you my featureCounts result, it looks like this. It's too low.
[1]: /media/images/eb8293fe-e6ae-4b02-92e2-0ba2075b
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samtools addreplacerg is for read groups. This is not what OP asked.
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When I try ``` samtools addreplacerg -r "@CB\tID:$cell" -o $cell.bam $LINE``` the CB tag gets add to the header, but the tag in every line …
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ah ! and your code doesn't work because clinvar ID is not a rs-ID.
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$ cat input.rs
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You can try <https://github.com/inab/trimal>
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yes i want what rsem does and i did try with prior-enhanced option/pRSEM, but i think pRSEM is for chipseq data
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Thank you so much. Should i proceed for annotation step?
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