nf-core/hlatyping

adding HLA-VBseq as a new module

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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 allele sequences and abundance of reads on HLA alleles by variational Bayesian inference.

Original paper

https://pubmed.ncbi.nlm.nih.gov/25708870/

Source code/binary

http://nagasakilab.csml.org/hla/

Licence

The Licensee agrees to indemnify Tohoku University and hold Tohoku University harmless from and against any and all claims, damages and liabilities asserted by third parties (including claims for negligence) which arise directly or indirectly from the use of the Software or the sale of any products based on the Software.

That one sounds better in terms of licencing 👍🏻