Evidence map›Paper›PMID 42128011›Full record

ArticleBioinformatics (Oxford, England)2026

A novel method for across-chromosome phasing without relative data.

Emmanuel Sapin, Kristen M Kelly, Matthew C Keller

Abstract read
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Article in Bioinformatics (Oxford, England), 2026. 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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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Emmanuel SapinInstitute for Behavioral Genetics, University of Colorado Boulder, Boulder, CO 80309, United States.ORCID 0000-0002-7188-3715
Kristen M KellyInstitute for Behavioral Genetics, University of Colorado Boulder, Boulder, CO 80309, United States.
Matthew C KellerInstitute for Behavioral Genetics, University of Colorado Boulder, Boulder, CO 80309, United States.

Funding

Estimating the genetic and environmental architecture of psychiatric disordersR01MH100141 · NIMH · UNIVERSITY OF COLORADO · PI KELLER, MATTHEW CHARLES · 2013 to 2022
$5.3M
Causes and consequences of mental disorders: The environmental and genetic influences of parents on offspring.R01MH130448 · NIMH · UNIVERSITY OF COLORADO · PI Matthew Charles Keller · 2022 to 2026
$3.7M
NIMH NIH HHS 2R01 MH100141NIMH NIH HHS R01 MH100141NIMH NIH HHS R01 MH130448
6 · The paper itself

Abstract

motivationAcross-chromosome phasing identifies which haplotypes of different chromosomes come from the same parent. This differs from within-chromosome phasing, which uses linkage disequilibrium patterns to determine which alleles were co-inherited within each chromosome but does not match haplotypes across different chromosomes. While across-chromosome phasing can be conducted using genotypes from parents or close relatives, current methods perform poorly for samples of unrelated individuals. Here, we introduce a novel approach for across-chromosome phasing that employs a window-based SNP-similarity metric, eliminating the need for data from close relatives or detection of identical-by-descent haplotypes.

resultsUsing UK Biobank offspring with both parents genotyped as a gold standard, we evaluated the performance of our method by phasing the offspring without using parental data. In genomic data with no within-chromosome phase errors, our algorithm achieved a mean across-chromosome phasing accuracy of 95%, with 53% of individuals phased perfectly. When data was pre-phased computationally using a standard within-chromosome phasing algorithm, mean accuracy for across-chromosome phasing dropped to 83.1%. Thus, our method is limited primarily by the accuracy of within-chromosome phasing accuracy and can approach near-perfect across-chromosome phasing accuracy as within-chromosome phasing accuracy improves. AVAILABILITY AND IMPLEMENTATION: The implementation was executed within a multi-node computational environment of University of Colorado Boulder Research Computing (Blanca Cluster: https://www.colorado.edu/rc/resources/blanca), employing parallelization techniques in the C programming language. The source code has been made publicly accessible online at https://github.com/emmanuelsapin/AcrossChromosomesPhasing, thereby facilitating reproducibility of the results for researchers with authorized access to the UK Biobank dataset.

Indexed as

ChromosomesGenomicsAlgorithmsChromosome MappingHaplotypesHumansLinkage DisequilibriumPolymorphism, Single Nucleotide

Identifiers

PMID42128011
PMCPMC13198864

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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.