Evidence map›Paper›PMID 39975036›Full record

ArticlebioRxiv : the preprint server for biology2025

Haplotype Matching with GBWT for Pangenome Graphs.

Ahsan Sanaullah, Seba Villalobos, Degui Zhi, Shaojie Zhang

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In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Ahsan SanaullahDepartment of Computer Science, University of Central Florida, Orlando, FL, USA.
Seba VillalobosDepartment of Computer Science, University of Central Florida, Orlando, FL, USA.
Degui ZhiMcWilliams School of Biomedical Informatics, University of Texas Health Science Center at Houston, Houston, TX, USA.ORCID 0000-0001-7754-1890
Shaojie ZhangDepartment of Computer Science, University of Central Florida, Orlando, FL, USA.ORCID 0000-0002-4051-5549

Funding

Scalable methods for identity by descentR01HG010086 · NHGRI · YALE UNIVERSITY · PI Shaojie Zhang, Degui Zhi · 2018 to 2026
$4.9M
NHGRI NIH HHS R01 HG010086
6 · The paper itself

Abstract

Traditionally, variations from a linear reference genome were used to represent large sets of haplotypes compactly. In the linear reference genome based paradigm, the positional Burrows-Wheeler transform (PBWT) has traditionally been used to perform efficient haplotype matching. Pangenome graphs have recently been proposed as an alternative to linear reference genomes for representing the full spectrum of variations in the human genome. However, haplotype matches in pangenome graph based haplotype sets are not trivially generalizable from haplotype matches in the linear reference genome based haplotype sets. Work has been done to represent large sets of haplotypes as paths through a pangenome graph. The graph Burrows-Wheeler transform (GBWT) is one such work. The GBWT essentially stores the haplotype paths in a run length compressed BWT with compressed local alphabets. Although efficient in practice count and locate queries on the GBWT were provided by the original authors, the efficient haplotype matching capabilities of the PBWT have never been shown on the GBWT. In this paper, we formally define the notion of haplotype matches in pangenome graph-based haplotype sets by generalizing from haplotype matches in linear reference genome-based haplotype sets. We also describe the relationship between set maximal matches, long matches, locally maximal matches, and text maximal matches on the GBWT, PBWT, and the BWT. We provide algorithms for outputting some of these matches by applying the data structures of the r-index (introduced by Gagie et al.) to the GBWT. We show that these structures enable set maximal match and long match queries on the GBWT in almost linear time and in space close to linear in the number of runs in the GBWT. We also provide multiple versions of the query algorithms for different combinations of the available data structures. The long match query algorithms presented here even run on the BWT in the same time complexity as the GBWT due to their similarity.

Indexed as

BWTGBWTHaplotype MatchingIdentity by DescentLong MatchMEMPangenome GraphPBWTSet Maximal Match

Identifiers

PMID39975036
PMCPMC11838520

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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.