Evidence map›Paper›PMID 42817961›Full record

ArticlebioRxiv : the preprint server for biology2026

Inversion characterization in

Diana Tataru, Kira Vasquez-Kapit, Patrik Nosil, Zachariah Gompert

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

4 authors.

Diana TataruDepartment of Biology, Utah State University, Logan, UT, USA.ORCID 0000-0003-2632-2262
Kira Vasquez-KapitDepartment of Biology, Colorado State University, Fort Collins, CO, USA.ORCID 0009-0005-6699-2510
Patrik NosilStation d'Écologie Théorique et Expérimentale (SETE), CNRS; Moulis, 09200, France.ORCID 0000-0002-8271-9005
Zachariah GompertDepartment of Biology, Utah State University, Logan, UT, USA.ORCID 0000-0003-2248-2488

Funding

Predoctoral Training in Quantitative Cell & Molecular BiologyT32GM132057 · NIGMS · COLORADO STATE UNIVERSITY · PI Karen Marie Dobos, Brian Munsky · 2019 to 2026
$2.9M
Phenotypic and adaptive consequences of chromosomal rearrangementsR35GM158189 · NIGMS · UTAH STATE UNIVERSITY · PI Zachariah Gompert · 2025 to 2026
$760k
NIGMS NIH HHS R35 GM158189NIGMS NIH HHS T32 GM132057
6 · The paper itself

Abstract

Structural variants (SVs) can strongly influence evolutionary processes by suppressing recombination to create jointly inherited regions and by altering gene expression and the 3D organization of DNA. Recent improvements in sequencing technologies have led to an influx of high-resolution genomic data, bolstering research on SVs. When detecting and characterizing SVs, researchers face trade-offs in data and methods concerning scale, resolution, and computational intensity. Here, we evaluate such trade-offs by quantifying how data type, analytical approach, and SV attributes affect the ability to detect and characterize SVs in

Indexed as

comparative alignmentinversionslocal population structurepangenomestructural genomic variation

Identifiers

PMID42817961
PMCPMC13622062

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.