Hi Heng,
I have one sample with PE100 sequence data, and it's multi-lane PE data like "sample.L01.read_1.fq.gz, sample.L01.read_2.fq.gz, sample.L02.read_1.fq.gz sample.L02.read_1.fq.gz". I want to call small variants and structural variations by using all clean data.
how should do?
Hi Heng,
I have one sample with PE100 sequence data, and it's multi-lane PE data like "sample.L01.read_1.fq.gz, sample.L01.read_2.fq.gz, sample.L02.read_1.fq.gz sample.L02.read_1.fq.gz". I want to call small variants and structural variations by using all clean data.
how should do?