Comments (4)
This issue was raised in issue #11 it is due to file read mode "rU" being removed in Python 3.11
I've fixed this on the main branch of this repo but haven't pushed updates to conda and pypi yet.
In the meantime, clone the repo and do a local pip install like this:
git clone https://github.com/Adamtaranto/teloclip.git && cd teloclip && pip install -e .
Or run in a conda env with an earlier version of Python.
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Thanks for your reply, now it works with test data.
i am using my own data now, I got another issue:
[$]~> teloclip --ref V5.male.fasta.fai male.minimap2.sam
@pg ID:minimap2 PN:minimap2 VN:2.17-r941 CL:minimap2 -ax map-ont /ebio/scratch/fhaas/Ec_nanopore/Ec32/basecall_Ec32_modbase_all_super_V3/pass/Ec32_all.fasta V5.male.fasta
Reference sequence not found in FAI file: 58e481aa-cb3d-418f-9194-fc89512d369e
saying i didn't build index for my genome, actually i build the index(samtools faidx V5.male.fasta), do you have any idea about this?
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Can you post the contents of your fai
index file, and also the headers and first couple of alignments from your sam
file.
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Thanks a lot. I found an issue with my script, and now I have solved it. Thank you so much for the promotion!!!
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Related Issues (20)
- Automatically extend contigs HOT 1
- error "invalid mode: 'rU' " in teloclip (v. bioconda)
- Refresh codebase
- Automate testing HOT 1
- Package Distribution HOT 1
- Feature: Align and Extend HOT 5
- Improve readability
- Confusing about input and output file HOT 17
- Feature: Fuzzy motif search
- Add metadata to extracted overhang reads HOT 1
- Missing isMotifInClip()
- Could you explain in detail how to extend reads? HOT 3
- Calculate alignment end position from CIGAR HOT 1
- Verify: Correct read slice coords for negative strand alignments HOT 2
- Summary report option
- Interactive Contig extension HOT 1
- functionality to extract reads at NNN gaps in scaffolds? HOT 2
- NNNNN reads HOT 8
- Find existing telo repeats in contigs HOT 1
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