RIN was measured by the sequencing company. I have submitted my sample for NGS to the company and they provided me RIN Value.
The thing is, While i was working with the same sample for RT-PCR, with my own designed primers, we were able to amplify almost half of the genome from the same sample.
So my concern is, if the viral RNA is degraded , how come we were able to amplify! Will it not be possible to perform NGS on same sample?