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Recent Replies
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biofalconch
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Hey, if you arelady have the barcodes, you could use samtools
`samtools view -h -b -f CB:Z:TAAGAGATCCTATGTT > TAAGAGATCCTATGTT.bam`
Hope…
Answer: How to split a scRNA reads BAM or FASTQ file to a separate file for each cell by
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biofalconch
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Here is a code that should work, but just like everyone else in the comments I'm a little confused why would you need to separate them:
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check you have a complete environment for GATK , including the python module "keras". https://gatk.broadinstitute.org/hc/en-us/articles/360…
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Did you have any luck in splitting the BAM file based on the 10x cell barcode? I would like to split a BAM file based to only include 5 spe…
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genomation is based on GenomicRanges which uses 1-based coordinates. https://www.biostars.org/p/84686/
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I cannot speak for this package but I recommend clusterProfiler where the universe argument isindeed all tested genes so your background.
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You cannot derive enhancers from methylation profiles. Enhancers are regulatory elements, and they either are methylated or not. There is l…
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Cross-posted and answered there : https://stackoverflow.com/questions/76388032/convert-data-frame-with-character-column-to-data-frame-with-…
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Your question lacks precision, we do not know what you are talking about
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If you want to find enrichment of your selected genes versus the superset of all genes detected, then yes you mean the background. And to d…
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hi ,you can look at this fig in software **mosdepth** . By traversing a sorted BAM file from the beginning, one can obtain depth informat…
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You should probably not advertise your personal email. It is not needed to understand the code.
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[seqkit common](https://bioinf.shenwei.me/seqkit/usage/#common) finds common sequences of multiple files by id/name/sequence
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