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2.1 years ago by
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2.1 years ago by
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updated 2.1 years ago by
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written 2.1 years ago by
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sorry, I have mistaken samtools with spades... running `samtools view -h...` did the trick. Thank you.
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Thank you for the response! Unfortunately this is completely independent and not part of a course. I was asking for some innovative ways to…
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The XX and XY counts are present on any given variants page.
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There are many ways to do normalization and one of the correct ways is simply to plug raw counts into deseq2 (the math that deseq2 uses to …
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Is it the version number in your data?
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Thanks a lot for your answer. I will check the paper.
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If those logFCs are different, then that's a normalization issue.
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Thanks both for your input. It got me to look at the published methodologies more closely, and you guys were right. One paper that I was re…
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Yes it does not match at all, and those genes that are common in both analysis results have very different logFC and p values
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