Describe the bug
I successfully generated the reference according to "xpresspipe curateReference -o /path/to/reference -f /path/to/reference/genome_fastas -g /path/to/reference/transcripts.gtf"
Then I process the dataset according to "xpresspipe riboseq -i /path/to/input -o /path/to/output -r /path/to/reference/ --gtf /path/to/reference//transcripts_CT.gtf -e ribo"
The "triming", "QC" can be completed, but the alignment can not.
Error as shown as: "ValueError: file has no sequences defined (mode='r') - is it SAM/BAM format? Consider opening with check_sq=False"
Desktop (please complete the following information):
Hi,
Sorry for the delay. Could you provide me a sample FASTQ file, along with any log files you receive? You can email them to me at jordanberg.contact@gmail.com
Describe the bug I successfully generated the reference according to "xpresspipe curateReference -o /path/to/reference -f /path/to/reference/genome_fastas -g /path/to/reference/transcripts.gtf"
Then I process the dataset according to "xpresspipe riboseq -i /path/to/input -o /path/to/output -r /path/to/reference/ --gtf /path/to/reference//transcripts_CT.gtf -e ribo"
The "triming", "QC" can be completed, but the alignment can not.
Error as shown as: "ValueError: file has no sequences defined (mode='r') - is it SAM/BAM format? Consider opening with check_sq=False"
Desktop (please complete the following information):