Entering edit mode
wang peter
★
2.0k
@wang-peter-4647
Last seen 10.3 years ago
dear all:
i have non-strand specific RNA-seq samples for
edgeR analysis.
first, i used bowtie to map my reads to the
assembled contigs to count the sample. then for each
contig, i got two number. one is forward count, the
other is reverse count.
if i sum these two number together to get one
count number for edgeR input. is it right?
should i sum them or average them
--
shan gao
Room 231(Dr.Fei lab)
Boyce Thompson Institute
Cornell University
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