Evidence map›Paper›PMID 38089113›Full record

ArticleBioinformatics advances2023

XHap: haplotype assembly using long-distance read correlations learned by transformers.

Shorya Consul, Ziqi Ke, Haris Vikalo

Abstract read
In one paragraph

Article in Bioinformatics advances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Shorya ConsulDepartment of Electrical and Computer Engineering, The University of Texas at Austin, Austin, TX 78712, United States.ORCID https://orcid.org/0000-0001-9137-8989
Ziqi KeDepartment of Electrical and Computer Engineering, The University of Texas at Austin, Austin, TX 78712, United States.
Haris VikaloDepartment of Electrical and Computer Engineering, The University of Texas at Austin, Austin, TX 78712, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Summary: Reconstructing haplotypes of an organism from a set of sequencing reads is a computationally challenging (NP-hard) problem. In reference-guided settings, at the core of haplotype assembly is the task of clustering reads according to their origin, i.e. grouping together reads that sample the same haplotype. Read length limitations and sequencing errors render this problem difficult even for diploids; the complexity of the problem grows with the ploidy of the organism. We present XHap, a novel method for haplotype assembly that aims to learn correlations between pairs of sequencing reads, including those that do not overlap but may be separated by large genomic distances, and utilize the learned correlations to assemble the haplotypes. This is accomplished by leveraging transformers, a powerful deep-learning technique that relies on the attention mechanism to discover dependencies between non-overlapping reads. Experiments on semi-experimental and real data demonstrate that the proposed method significantly outperforms state-of-the-art techniques in diploid and polyploid haplotype assembly tasks on both short and long sequencing reads. Availability and implementation: The code for XHap and the included experiments is available at https://github.com/shoryaconsul/XHap.

Identifiers

PMID38089113
PMCPMC10713121

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Registered trials

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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.