Closed ruy-jauregui closed 1 year ago
Hello! I run these commands: seqtk sample -s100 cJ288_1.fq 90000 > ./subsample/cJ288_1.fq seqtk sample -s100 cJ288_2.fq 90000 > ./subsample/cJ288_2.fq
When I count the reads in the output I get: cJ288_1.fq:89995 cJ288_2.fq:89998
What's going on?
Probably the input fastq are not paired.
Hello! I run these commands: seqtk sample -s100 cJ288_1.fq 90000 > ./subsample/cJ288_1.fq seqtk sample -s100 cJ288_2.fq 90000 > ./subsample/cJ288_2.fq
When I count the reads in the output I get: cJ288_1.fq:89995 cJ288_2.fq:89998
What's going on?