Question: Bowtie
0
Sher, Falak • 80 wrote:
Hi Experts,
I have single end Illumina reads from ChIP-Seq experiment. The files
have encoding Illumina 1.5, and the sequence length is 76bp.
After basic FastQc I want to map the sequences using Bowtie. My
question is:
do I need to split my reads (farward and backward) before running
mapping tool?
In one of Galaxy screen shorts reads are spitted while not in the
other.
Thank you in advance,
F
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modified 7.6 years ago
by
Jennifer Hillman Jackson ♦ 25k
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written
7.6 years ago by
Sher, Falak • 80
