Evidence map›Paper›PMID 40894736›Full record

ArticlebioRxiv : the preprint server for biology2025

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 readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. 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.

Matthew Musat
Mihir Junaghare
Asad Ahmad
Mehlum Ali
Sebastian Alves
Sreeram Pasupuleti
Jelisha Perera
Omar Saada
Brady Sabido
Trevor Smith
Sophie Walz
Mahul ChakrabortyORCID 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 in all organisms; yet, many SVs evade discovery using short reads. While long-read sequencing can find the hidden SVs, the role of SVs in variation in organismal traits remains largely unclear. To address this gap, we investigate the molecular basis of 50 classical phenotypes in 11

Identifiers

PMID40894736
PMCPMC12393429

What OpenQuestion holds

Textmetadata
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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.