Evidence map›Paper›PMID 42623377›Full record

ArticlePLoS computational biology2026

A portable recalibration workflow for reference-based variant calling in non-human genomes.

Hyeonjung Lee, Sunhee Kim, Michelle Audrelia Sunartha, Chang-Yong Lee, Young-Suk Lee

Abstract read
In one paragraph

Article in PLoS computational 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.

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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

5 authors.

Hyeonjung LeeDepartment of Bio and Brain Engineering, Korea Advanced Institute of Science and Technology, Daejeon, Republic of Korea.
Sunhee KimDepartment of Industrial and Systems Engineering, Kongju National University, Cheonan, Republic of Korea.
Michelle Audrelia SunarthaDepartment of Bio and Brain Engineering, Korea Advanced Institute of Science and Technology, Daejeon, Republic of Korea.
Chang-Yong LeeDepartment of Industrial and Systems Engineering, Kongju National University, Cheonan, Republic of Korea.ORCID 0000-0003-1778-6532
Young-Suk LeeDepartment of Bio and Brain Engineering, Korea Advanced Institute of Science and Technology, Daejeon, Republic of Korea.ORCID 0000-0003-0220-9951

Funding

Basic Science Research Program through the National Research Foundation (NRF) of KoreaBio&Medical Technology Development Program of the National Research Foundation (NRF)
6 · The paper itself

Abstract

A key computational step in reference-based variant calling is distinguishing true genetic variants from sequencing errors. Advanced tools and workflows have been developed to handle this by computational modelling of technical errors from the sequencing machines. However, these recalibration workflows have largely been evaluated for human data only and its exact applicability for non-human data remains unknown. Here, we conducted a systematic evaluation of variant calling on human, rice, sheep, and chickpea data, and found that existing workflows introduce unexpected statistical bias, thus leading to suboptimal variant calls for non-human data. To address this problem, we present simple guidelines for constructing a "pseudo-"database (pseudoDB) of genetic variants as a scalable and portable solution for recalibration and variant calling. With human data, our pseudoDB-based workflow performs comparably to existing dbSNP-based GATK3 workflows and those using DeepVariant, Strelka2, and FreeBayes. We extend this to other non-human genomes, namely cattle, brown bear, swan goose, African oil palm, Komodo dragon, and stevia, altogether resulting in the identification of up to 242.0% unique genetic variants. The majority of newly identified variants are within the non-coding regions, hinting at the rich diversity of genome regulation in the non-human population. Our pseudoDB-based workflow is agnostic to reference genomes and modular for easy integration with other computational workflows for human and non-human resequencing data.

Indexed as

Genetic VariationGenomeGenomicsAnimalsCalibrationCattleComputational BiologyDatabases, GeneticHumansPolymorphism, Single NucleotideSequence Analysis, DNASheepWorkflow

Identifiers

PMID42623377
PMCPMC13492802

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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.