In RNA-seq data analysis, after alignment, the most common step is to estimate gene or/and transcript expression abundance, the expression level is represented by read counts. There are three options in this step:
Quantify to annotation model (Partek E/M)
Quantify to transcriptome (Cufflinks)
Quantify to reference (Partek E/M)
Quantify regions
HTSeq
Count feature barcodes
Salmon
Last updated 1 year ago
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