Hi,
do you use a some rule for trimming/removing or saving reads with the worst quality for DNA and RNA assembly/alignment. How do you decide to trimm/remove/save? According the type of analysis, coverage, base quality.... ???? Thanks a lot.
do you use a some rule for trimming/removing or saving reads with the worst quality for DNA and RNA assembly/alignment. How do you decide to trimm/remove/save? According the type of analysis, coverage, base quality.... ???? Thanks a lot.
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