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Questions related from Francesco Antonio Tucci
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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