Evidence map›Paper›PMID 42134987›Full record

ArticleGenome research2026

Structural variants are enriched in deleterious visible phenotypes in

Alejandra Samano, Matthew Musat, Mihir Junaghare, Asad Ahmad, Mehlum Ali, Sebastian Alves, Sreeram Pasupuleti, Jelisha Perera, Omar Saada, Brady Sabido and 3 more

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Genome research, 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

5 · Who and what money

Authors and funding

13 authors.

Alejandra SamanoDepartment of Biology, Texas A&M University, College Station, Texas 77843, USA.ORCID http://orcid.org/0009-0003-4460-0737
Matthew MusatDepartment of Biology, Texas A&M University, College Station, Texas 77843, USA.
Mihir JunaghareDepartment of Biology, Texas A&M University, College Station, Texas 77843, USA.
Asad AhmadDepartment of Biology, Texas A&M University, College Station, Texas 77843, USA.
Mehlum AliDepartment of Biology, Texas A&M University, College Station, Texas 77843, USA.
Sebastian AlvesDepartment of Biology, Texas A&M University, College Station, Texas 77843, USA.
Sreeram PasupuletiDepartment of Biology, Texas A&M University, College Station, Texas 77843, USA.
Jelisha PereraDepartment of Biology, Texas A&M University, College Station, Texas 77843, USA.
Omar SaadaDepartment of Biology, Texas A&M University, College Station, Texas 77843, USA.
Brady SabidoDepartment of Biology, Texas A&M University, College Station, Texas 77843, USA.
Trevor SmithDepartment of Biology, Texas A&M University, College Station, Texas 77843, USA.
Sophie WalzDepartment of Biology, Texas A&M University, College Station, Texas 77843, USA.
Mahul ChakrabortyDepartment of Biology, Texas A&M University, College Station, Texas 77843, USA mahul@tamu.edu.ORCID http://orcid.org/0000-0003-2414-9187

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genome structural variants (SVs) comprise a sizable portion of functionally important genetic variation, yet many evade discovery using short reads. Although long-read sequencing can reveal hidden SVs, their contribution to organismal trait variation remains unclear. To address this gap, we investigate the molecular basis of 50 classical phenotypes in 11

Identifiers

PMID42134987
PMCPMC13322080

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Registered trials

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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.