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- A: what are the big questions in bioinformatics field nowadays
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- C: what are the big questions in bioinformatics field nowadays
- A: How To Remove The Same Sequences In The Fasta Files?
- How To Remove The Same Sequences In The Fasta Files?
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Recent Replies
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C: From Impute2 to PLINK: when to merge chromosome files? by
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Hi, I have used this option to merge two chromosomes as an example. I'm getting a difference in n...
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zhuobaowen • 0
you are right, thank you so much!
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If you know the gene id you can use [seqkit grep][1]. [1]: https://bioinf.shenwei.me/seqkit/u...
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If you mean to round floating numbers, you can use round() in R.
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You mean you want to make sure all chunks' reads are not overlapped (which means one alignment oc...
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You can use featurecounts directly on the BAM file which is what the tutorial is doing. Then you ...
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How would you alter the command if there are two digits after the decimal point, say ENSG00000000...
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It might be better to ask this on https://support.bioconductor.org/ - the developer is more activ...
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The arrows point to the predicted future state of their respective cells. > Second thing, can...
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I used a software called kallisto , it generate a count and TPM matrix, then i used DESeq2 to fin...
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I used TissueFAXS Plus system to scan whole testis section , this technic can count all cell(by s...
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Please ask Maria for the exact command that she used, and the version of VEP.
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