Dear all,
I would like to know the recommendation of number of reads (coverage) for the splice QTL detection (from RNA seq data).
Here (https://genohub.com/recommended-sequ...y-application/) they reccomend about 50-100M reads for alternative splicing.
What do you think?
thanks
Clarissa
I would like to know the recommendation of number of reads (coverage) for the splice QTL detection (from RNA seq data).
Here (https://genohub.com/recommended-sequ...y-application/) they reccomend about 50-100M reads for alternative splicing.
What do you think?
thanks
Clarissa