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tarek.mohamed • 250
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WouterDeCoster ♦ 39k
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Kevin Blighe ♦ 44k
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written 2.5 years ago by
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Pierre Lindenbaum ♦ 120k
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newDNASeqer • 630
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Malachi Griffith ♦ 17k
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newDNASeqer • 630
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written 6.1 years ago by
Matt Miossec • 320
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vdauwera • 920
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C: DESeq2 - Warning message by
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Hi Michael, I am running DESeq2 v1.22.2 for a dataset with 30 samples. I have been getting simil...
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So next step is apply plink --a1-allele to change the reference allele?
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Thanks, but I didn't quite get it. Do you mean I need to change v1 <- X[ , i] to v1 <...
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Please edit your post and add the job location (city, state/province, country) to the title.
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Ehm yes it should change those. That is exactly what I asked for.
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Please see https://www.biostars.org/p/309884/ to add your images properly. You need **the direct ...
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OP says > I want to do DeSeq2 Your advice is to > use featurecounts I don't see how t...
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Whatever works for you, my friend. Programming languages give you the freedom to implement proble...
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This script is nice to identify the variants whose REF allele is not correct and should be revise...
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I don't recall initiating a conversation on GATK Forums, unfortunately. We were collaborating wit...
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You can use featurecounts (http://bioinf.wehi.edu.au/featureCounts/) to generate read count.
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> https://science.sciencemag.org/content/335/6070/823 > > A Systematic Survey of Loss-o...
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