We have generated a set of RNA-seq samples. These are human PE samples with read length of 150bp. We would like to identify the total number of genes that could be detected by reducing the number of reads to 1/2, 1/3rd and 1/4th. After this, identify the differentially expressed genes between the two conditions i.e. before/after treatment.
Subsampling aligned SAM/BAM files for RNA-seq analysis
Hi,
I would like to know if there are any specific tools to sub-sample aligned SAM or BAM files. What type of files could be considered for the sub-sampling sorted or unsorted SAM or BAM files.
Thank you, Toufiq
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