Hi,
When check the unique.coverage.csv file of the genes, the average coverage is around 5000, how to link this to the actual X coverage that we usual say about NGS, for NGS it only ranges to ~ 100X , is that right ?
Does this have to take the length of the reference sequence into consideration?
Thanks,
When check the unique.coverage.csv file of the genes, the average coverage is around 5000, how to link this to the actual X coverage that we usual say about NGS, for NGS it only ranges to ~ 100X , is that right ?
Does this have to take the length of the reference sequence into consideration?
Thanks,
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