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pacbio • reset2
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lieven.sterck ♦ 6.0k
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h.mon ♦ 27k
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written 13 months ago by
from the mountains • 80
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written 4 months ago by
tbeignier • 0
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stolarek.ir • 600
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written 7 months ago by
shelkmike • 130
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7 months ago by
Devon Ryan ♦ 92k
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C: Multiple Sequence Alignment viewers or How to Build a Conservation Plot by
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It worked with conda afterall.
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That's fine, it can still merge them and will even help you determine which caller called which v...
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Thanks for your reply, So for [this][1] dataset the authors have provided a file "GSE28521_RAW.ta...
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They should be from the same sample. Does this make a difference? To provide some clarification...
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jared.andrews07 • 3.3k
[bcftools `merge`](https://samtools.github.io/bcftools/bcftools.html) is likely what you want. It...
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You can trust the results, but you have to be careful about the contrasts to get what you want. I...
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Please use `ADD REPLY/ADD COMMENT` to keep threads logically organized. This comment belongs unde...
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In addition to the documentation and papers describing the tool, the ultimate description of the ...
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[@Kristoffer][1] Many thanks for this information. I have processed around 700 A. thaliana access...
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I will never understand why authors do not simply upload the raw count matrix. These RPKM-whateve...
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Since they did not deposit RAW counts, you better reanalyze the FASTQ deposited files if you want...
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