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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.
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Description of feature
Algorithm/tool short description
Original paper
https://pubmed.ncbi.nlm.nih.gov/25708870/
Source code/binary
http://nagasakilab.csml.org/hla/
Licence
The text was updated successfully, but these errors were encountered: