Entering edit mode
5 months ago
bioinfo1994
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20
Hello. I have paired-end mRNA sequencing data with an average read length of 75 bp. My end goal is to analyze gene expression and perform variant calling to identify SNVs. I would appreciate your guidance on when to use a genome reference and when to use a transcriptome reference (with a splice-aware aligner) for these two tasks and in general, along with the reasoning behind each choice. Thank you so much!