Hi,
I'm just aligning a MiSeq fastq run to a custom index and am getting the following error:
FASTQ read name is too long; read names must be 1022 characters or fewer.
Beginning of bad read name:
terminate called after throwing an instance of 'int'
/local/scratch/1426970873.9330346: line 8: 25641 Aborted
I cant find anything online and am not sure how to fix this. Any thoughts?
I'm just aligning a MiSeq fastq run to a custom index and am getting the following error:
FASTQ read name is too long; read names must be 1022 characters or fewer.
Beginning of bad read name:
terminate called after throwing an instance of 'int'
/local/scratch/1426970873.9330346: line 8: 25641 Aborted
I cant find anything online and am not sure how to fix this. Any thoughts?
Comment