henhaobio
Sign in

Frontiers in ImmunologyGenomicsPeer-reviewed journal article

AIRR-C Human IG Reference Sets: curated sets of immunoglobulin heavy and light chain germline genes

Andrew M. CollinsiD, Mats OhliniD, Martin CorcoraniD, James HeatheriD, Duncan RalphiD, Mansun LawiD, Jesús Martínez-BarnetcheiD, Jian YeiD, Eve RichardsoniD, William S. GibsoniD, Oscar L. RodrigueziD, Ayelet PeresiD, Gur YaariiD, Corey T. WatsoniD, William LeesiD

PDFDOIPreprint

Abstract

Analysis of an individuals immunoglobulin (IG) gene repertoire requires the use of high-quality germline gene Reference Sets. The Adaptive Immune Receptor Repertoire-Community (AIRR-C) Reference Sets have been developed to include only human IG heavy and light chain alleles that have been confirmed by evidence from multiple high-quality sources. By including only those alleles with a high level of support, including some new sequences that currently lack official names, AIRR-seq analysis will have greater accuracy and studies of the evolution of immunoglobulin genes, their allelic variants and the expressed immune repertoire will be facilitated. Although containing less than half the previously recognised IG alleles (e.g. just 198 IGHV sequences), the Reference Sets eliminated erroneous calls and provided excellent coverage when tested on a set of repertoires from 99 individuals comprising over 4 million V(D)J rearrangements. To improve AIRR-seq analysis, some alleles have been extended to deal with short 3 or 5 truncations that can lead them to be overlooked by alignment utilities. To avoid other challenges for analysis programs, exact paralogs (e.g. IGHV1-69*01 and IGHV1-69D*01) are only represented once in each set, though alternative sequence names are noted in accompanying metadata. The Reference Sets also include novel alleles: 8 IGHV alleles, 2 IGKV alleles and 5 IGLV alleles. The version-tracked AIRR-C Reference Sets are freely available at the OGRDB website (https://ogrdb.airr-community.org/germline_sets/Human) and will be regularly updated to include newly-observed and previously-reported sequences that can be confirmed by new high-quality data.

Citations
28
FWCI
4.66
Field percentile
top 4%

Reproducibility ledger

Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.

Sign in to file a reproducibility report.

Similarity Map
SelectedSame fieldCross-field
THISYang '26Gadala-Mari '19Peres '26Lin '20Ford '22Peres '22
73% semantic matchGenomics
Yu-Hsuan Yang, Chi‐Yuan Yao, Mao-Jan Lin+11 more·Journal of Advanced Research·Jan 30, 2026· 3 citations