Evidence map›Paper›PMID 42647746›Full record

ArticleMolecular biology and evolution2026

Variant calling in nonmodel organisms with snpArcher.

Cade Mirchandani, Abdelmajid Omarjee, Guillaume Achaz, Erik D Enbody, Gregg W C Thomas, Timothy B Sackton

Abstract read
In one paragraph

Article in Molecular biology and evolution, 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

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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

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

6 authors.

Cade MirchandaniDepartment of Biomolecular Engineering, University of California, Santa Cruz, Santa Cruz, CA 95064, USA.ORCID 0009-0002-1970-430X
Abdelmajid OmarjeeStochastic Models for the Inference of Life Evolution (SMILE), CIRB, Collège de France, Université PSL, CNRS, INSERM, Paris 75005, France.ORCID 0009-0002-6919-7297
Guillaume AchazStochastic Models for the Inference of Life Evolution (SMILE), CIRB, Collège de France, Université PSL, CNRS, INSERM, Paris 75005, France.ORCID 0000-0003-4514-5935
Erik D EnbodyDepartment of Computational Biology, Cornell University, Ithaca, NY 14853, USA.ORCID 0000-0003-1349-628X
Gregg W C ThomasInformatics Group, Harvard University, Cambridge, MA 02138, USA.ORCID 0000-0001-7621-2980
Timothy B SacktonInformatics Group, Harvard University, Cambridge, MA 02138, USA.ORCID 0000-0003-1673-9216

Funding

National Science Foundation DEB-1754397
6 · The paper itself

Abstract

Population genomic studies in nonmodel organisms increasingly depend on whole-genome resequencing, yet translating raw reads into reliable variant callsets remains a practical challenge due to the complexity of multistep bioinformatics pipelines and the absence of species-specific best practices. Here, we present a step-by-step protocol for snpArcher, a Snakemake-based workflow that takes raw sequencing reads and a reference genome as input and produces a filtered, joint-called Variant Call Format (VCF) file suitable for downstream population genomic analysis. We guide users through six phases: installation and environment setup, sample sheet creation, run configuration, execution on local or high-performance computing systems, quality control review using an interactive HTML dashboard, and downstream analysis, focusing on postprocessing and filtering. The quality control (QC) dashboard aggregates individual-level metrics including principal component analysis, relatedness estimation, depth-missingness diagnostics, and admixture analysis to help identify batch effects, contamination, cryptic relatedness, and outlier samples before downstream analysis. We demonstrate the impact of sequential filtering steps on the site frequency spectrum and demographic inference using a dataset of 137 burrowing owl (Athene cunicularia) genomes, showing how removal of low-coverage individuals, sex-linked scaffolds, and regions of excess heterozygosity eliminates artifacts that would otherwise bias inference of population size history. This protocol is intended as a practical companion to the original snpArcher publication, enabling researchers working with nonmodel organisms to produce and evaluate analysis-ready variant callsets in a reproducible manner.

Indexed as

SoftwareStrigiformesAnimalsComputational BiologyGenetics, PopulationPolymorphism, Single Nucleotidebioinformaticsnonmodel speciespopulation genetics

Identifiers

PMID42647746
PMCPMC13590228

What OpenQuestion holds

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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.