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Questions related from Francesco Antonio Tucci
Library preparation for single cells RNA sequencing ends being the most expensive part of the of the process, so it's way cheaper doubling the reads depth than the number of samples. I have seed...
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Hi, I'm doing variant calling from my RNAseq data on a cell line (Paired End 2X100b, Illumina) I'm following GATK workflows and everything is working almost fine since I can find all the expected...
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Whenever I try to add a reference fasta file for computing the GC content in the GetBamCounts function: my.countsV6
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I hope you can give me some insights on the right direction to pursue and on some bioinformatic tools I'm ignoring to solve the following bioinformatic problem: I got involved in a cancer research...
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