Closed sdwien closed 5 years ago
Dear Sophia,
The number of reads in the fastq files is between 15-20 millions. This is a good number for gene expression quantification. Check also https://support.illumina.com/bulletins/2017/04/considerations-for-rna-seq-read-length-and-coverage-.html
Best wishes,
Gianni
Dear Gianni, I would like to know how many read you used for the analysis in the paper, or how many reads you would consider the minimum number, a good number or more than enough for the analysis? Thanks and best, Sophia