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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?
The text was updated successfully, but these errors were encountered:
Probably the input fastq are not paired.
Sorry, something went wrong.
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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?
The text was updated successfully, but these errors were encountered: