Evidence map›Paper›PMID 42079165›Full record

ArticlebioRxiv : the preprint server for biology2026

A Benchmark of Modern Statistical Phasing Methods.

Andrew T Beck, Hyun Min Kang, Sebastian Zöllner

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Andrew T BeckDepartment of Biostatistics, University of Michigan, Ann Arbor, 48108, MI, United States of America.ORCID 0000-0002-2516-2423
Hyun Min KangDepartment of Biostatistics, University of Michigan, Ann Arbor, 48108, MI, United States of America.ORCID 0000-0002-3631-3979
Sebastian ZöllnerDepartment of Biostatistics, University of Michigan, Ann Arbor, 48108, MI, United States of America.

Funding

Leveraging long-range haplotypes in sequencing data to advance large scale genetic studiesR01HG011031 · NHGRI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ZOELLNER, SEBASTIAN · 2020 to 2023
$1.4M
NHGRI NIH HHS R01 HG011031
6 · The paper itself

Abstract

Modern statistical phasing methods efficiently and accurately infer haplotype phase in large genomic samples, and their performance is critical for downstream analyses. However, rigorously evaluating phasing accuracy remains challenging. Here we demonstrate the use of synthetic diploids generated from male X chromosome sequences to benchmark and compare three commonly-used phasing methods: Beagle 5.4, SHAPEIT 4, and Eagle v2.4.1. Our evaluation reveals highly correlated error rates across all methods, although we observe distinct variation among methods within error types. Specifically, Eagle v2.4.1 is characterized by a higher frequency of switch errors, whereas SHAPEIT 4 displays a higher rate of flip (double-switch) errors. These patterns are consistent across diverse populations. Additionally, we observe an enrichment of errors at both CpG sites and rare variant sites, particularly for flip errors. Validating these results in autosomal trio data, we observe similar trends between the methods and error patterns, though with an increased flip error rate, a discrepancy that may be biased by genotype error.

Identifiers

PMID42079165
PMCPMC13131814

What OpenQuestion holds

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LicenceCC BY
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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.