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Hi genomepy team,
First, I want to say thanks for this software. Second, I have a question related to the `genome install` command - is there a way to install several genomes at a time instead of i…
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Add support for stitching multi-contig input files:
- [x] Genome selection in UI
- [x] Integrate Mauve Contig Mover into Galaxy
- [x] Create stitcher tool
- [ ] Collapse multiple source annotati…
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Features:
- [ ] Hox gene validation
- [ ] Cluster validation
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Given a circular reference genome for a prokaryote like E.coli, I don't think we should ever have dummy nodes, but given the way we generate the kmers, we might. This is more of a practical considera…
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Hi!!
I'm curated a genome with PretextView. I organized the map and tagged some unlocs with the M option and finally tagged the chromosomes with S mode. When I export the map to agp, a map.pretext.…
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Thanks for the good material. I have a question about the alignment using bowtie2, here according to [`mutation_sequencing_analysis_script.sh`](https://github.com/aldob/iMUT-seq/blob/4476db76f2058d0af…
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this might be of use to people looking to grok genome overlaps etc.
[notebook permalink](https://github.com/dib-lab/genome-grist/blob/051a96210958afcf7f1d61ce11537796339dc64e/hash-upsetr-example.ip…
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### Research
- [X] I have searched the documentation and previously asked questions.
### Question about nf-flu
I've been successful in using NF-flu on flu A nd B sequencing data, but just got …
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I want to use the reference genome hg19 version for analysis,
The following error message is displayed
![image](https://github.com/DiltheyLab/HLA-LA/assets/160692531/c944ff5a-4a3a-4dbe-94fb-84d62d70…
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Can you provide a detailed explanation on how to run this process? I am a beginner and don't quite understand. Thank you very much
tttxd updated
3 weeks ago