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Recent Replies
Comment: Sequence quality drops in the 3' end of the left sequence in paired end. What co
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Asaf
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What machine? (Nextseq? Novaseq?) what library prep method?
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If you want the average expression, you should look at `AverageExpression` from seurat which returns the average instead of the sum. `Avera…
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You can also use **[Grabseqs][1]**.
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What you can do is use **SnapGene**
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Your log seems fine.
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Hi William,
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This isn't really the right place for this question.
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thank you very much for your response I'm really grateful !!
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But shouldn't quality drop at both 3'ends and not just on the left one?
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https://www.biostars.org/p/91624/
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is this what you are looking for?
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" you're forced to use it" this is sort of since I have use docker image and then pass the GSM id as list of input first to check if the th…
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I don't think this log is helpful. Can't you just get fastq download links via sra-explorer.info or the tool mentioned by @rob in his answe…
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Great! It looks like USER enzyme is used to cleave before the first read sequencing and formamidopyrimidine DNA N-glycosylase is used to cl…
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