Family based HLA imputation and optimization of haplo-identical transplants
Abstract
Recently, haplo-identical transplantation with multiple HLA mismatches has become a viable option for system cell transplants. Haplotype sharing detection requires imputation of donor and recipient. We show that even in high-resolution typing when all alleles are known, there is a 15% error rate in haplotype phasing, and even more in low resolution typings. Similarly, in related donors, parents haplotypes should be imputed to determine what haplotype each child inherited. We propose GRAMM (GRaph bAsed FaMilly iMputation) to phase alleles in family pedigree HLA typing data, and in mother-cord blood unit pairs. We show that GRAMM has practically no phasing errors when pedigree data are available. We apply GRAMM to simulations with different typing resolutions as well as paired cord-mother typings, and show very high phasing accuracy, and improved alleles imputation accuracy. We use GRAMM to detect recombination events and show that the rate of falsely detected recombination events (False Positive Rate) in simulations is very low. We then apply recombination detection to typed families to estimate the recombination rate in Israeli and Australian population datasets. The estimated recombination rate has an upper bound of 10-20% per family (1-4% per individual). GRAMM is available at: https://gramm.math.biu.ac.il/.
Keywords
Cite
@article{arxiv.2208.05882,
title = {Family based HLA imputation and optimization of haplo-identical transplants},
author = {Zuriya Ansbacher-Feldman and Sapir Israeli and Martin Maiers and Loren Gragert and Dianne De Santis and Moshe Israeli and Yoram Louzoun},
journal= {arXiv preprint arXiv:2208.05882},
year = {2022}
}
Comments
23 pages (20 + 3 of Supp. Mat.), 9 figures (6 + 3 of Supp. Mat.) Submitted to NAR (Nucleic Acids Research)