Evidence map›Paper›PMID 37548401›Full record

ArticleNucleic acids research2023

IGHV allele similarity clustering improves genotype inference from adaptive immune receptor repertoire sequencing data.

Ayelet Peres, William D Lees, Oscar L Rodriguez, Noah Y Lee, Pazit Polak, Ronen Hope, Meirav Kedmi, Andrew M Collins, Mats Ohlin, Steven H Kleinstein and 2 more

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.3field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 19 citations in OpenAlex.

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  4. Is the vaccination-induced B cell receptor repertoire predictable?Immunoinformatics (Amsterdam, Netherlands) · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 7 institutions in 5 countries.

Ayelet PeresFaculty of Engineering, Bar Ilan University, 5290002 Ramat Gan, Israel.ORCID 0000-0002-0188-7315
William D LeesInstitute of Structural and Molecular Biology, Birkbeck College, University of London, London, WC1E 7JE, UK.ORCID 0000-0001-9834-6840
Oscar L RodriguezDepartment of Biochemistry and Molecular Genetics, University of Louisville School of Medicine, Louisville, KY, 40202, USA.ORCID 0000-0002-4587-6124
Noah Y LeeProgram in Computational Biology & Bioinformatics, Yale University, New Haven, CT, 06511, USA.
Pazit PolakFaculty of Engineering, Bar Ilan University, 5290002 Ramat Gan, Israel.ORCID 0000-0001-8363-0734
Ronen HopeFaculty of Engineering, Bar Ilan University, 5290002 Ramat Gan, Israel.
Meirav KedmiDepartment of Pathology, Yale School of Medicine, New Haven, CT, 06520, USA.
Andrew M CollinsSchool of Biotechnology and Biomedical Sciences, University of New South Wales, Sydney, NSW 2052, Australia.
Mats OhlinDepartment of Immunotechnology Lund University, Lund, 221 00, Sweden.ORCID 0000-0002-5105-1938
Steven H KleinsteinProgram in Computational Biology & Bioinformatics, Yale University, New Haven, CT, 06511, USA.ORCID 0000-0003-4957-1544
Corey T WatsonDepartment of Biochemistry and Molecular Genetics, University of Louisville School of Medicine, Louisville, KY, 40202, USA.ORCID 0000-0001-7248-8787
Gur YaariFaculty of Engineering, Bar Ilan University, 5290002 Ramat Gan, Israel.ORCID 0000-0001-9311-9884
Bar-Ilan University · ILUniversity of Louisville · USYale University · USInstitute of Structural and Molecular Biology · GBLund University · SETel Aviv University · ILUNSW Sydney · AU

Funding

COMPUTATIONAL TOOLS FOR THE ANALYSIS OF HIGH-THROUGHPUT IMMUNOGLOBULIN SEQUENCING EXPERIMENTSR01AI104739 · NIAID · YALE UNIVERSITY · PI KLEINSTEIN, STEVEN H. · 2014 to 2022
$3.6M
NIAID NIH HHS R01 AI104739
6 · The paper itself

Abstract

In adaptive immune receptor repertoire analysis, determining the germline variable (V) allele associated with each T- and B-cell receptor sequence is a crucial step. This process is highly impacted by allele annotations. Aligning sequences, assigning them to specific germline alleles, and inferring individual genotypes are challenging when the repertoire is highly mutated, or sequence reads do not cover the whole V region. Here, we propose an alternative naming scheme for the V alleles, as well as a novel method to infer individual genotypes. We demonstrate the strengths of the two by comparing their outcomes to other genotype inference methods. We validate the genotype approach with independent genomic long-read data. The naming scheme is compatible with current annotation tools and pipelines. Analysis results can be converted from the proposed naming scheme to the nomenclature determined by the International Union of Immunological Societies (IUIS). Both the naming scheme and the genotype procedure are implemented in a freely available R package (PIgLET https://bitbucket.org/yaarilab/piglet). To allow researchers to further explore the approach on real data and to adapt it for their uses, we also created an interactive website (https://yaarilab.github.io/IGHV_reference_book).

Indexed as

GenomicsImmunoglobulin Heavy ChainsReceptors, Antigen, B-CellAllelesGenotypeImmunoglobulin Heavy ChainsReceptors, Antigen, B-Cell

Identifiers

PMID37548401
PMCPMC10484671
OpenAlexW4385620513

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.