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Precision HLA typing from next-generation sequencing data

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### Description of the bug Just noticed that when the pipeline is run with data from multiple libraries/runs, the pipeline produces results for each library/line separately which is a bit...

enhancement

### Description of the bug This test samplesheet seems to fail `check_samplesheet.py`. I removed the data and just provided the headers - see attached files below, but... ``` cat test.csv...

bug

### Description of feature ### Algorithm/tool short description > estimate the most probable HLA alleles at full (8-digit) resolution from whole-genome sequence data. HLA-VBSeq simultaneously optimizes read alignments to HLA...

enhancement

### Description of feature Hello, As described in #145, adding more typing tools could allow us (among other things) to set up a result combination algorithm. If you compare it...

enhancement

### Description of feature Hello. Because all typing tools have their limitations & advantages (datatype, reads length, read depth, resolution, type of genes typable, etc.), it could be interesting to...

enhancement

Only for required genome fasta / subset for HLA to make mapping much faster and less memory intensive.

enhancement

Hi! I have a problem with running this pipeline. It seems that it incorrectly chooses memory requirements for files. This is especially problematic with very big files. My biggest file...

enhancement

I've tried to use a custom reference file. I have a file in the fasta format. I used Yara tool (http://packages.seqan.de/yara) to repack the fasta file into a supported format....

enhancement

Version `2.14.1` of [nf-core/tools](https://github.com/nf-core/tools) has just been released with updates to the nf-core template. This automated pull-request attempts to apply the relevant updates to this pipeline. Please make sure to...