Evidence map›Paper›PMID 42282526›Full record

ArticlebioRxiv : the preprint server for biology2026

CLASH (Chromatin Loop Across-sample Score Harmonizer) quantifies the relative contributions of genetic variation, methylation, and CTCF occupancy on chromatin loop strength across individuals.

Valmik Ranparia, Human Genome Structural Variation Consortium, Geoffrey Fudenberg, Mark Jp Chaisson

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.

Valmik RanpariaDepartment of Quantitative and Computational Biology, University of Southern California, CA, USA.ORCID 0009-0002-0392-7269
Human Genome Structural Variation Consortium
Geoffrey FudenbergDepartment of Quantitative and Computational Biology, University of Southern California, CA, USA.ORCID 0000-0001-5905-6517
Mark Jp ChaissonDepartment of Quantitative and Computational Biology, University of Southern California, CA, USA.ORCID 0000-0001-5395-1457

Funding

Identifying and Characterizing the Full Spectrum of Haplotype-resolved Structural Variation in Human GenomesU24HG007497 · NHGRI · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI Evan Eichler, Jan Oliver Korbel · 2019 to 2026
$17.2M
Detection and genotyping complex human genetic variation using single-molecule sequencingR01HG011649 · NHGRI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Mark Chaisson · 2021 to 2026
$2.5M
NHGRI NIH HHS R01 HG011649NHGRI NIH HHS U24 HG007497
6 · The paper itself

Abstract

Three-dimensional genome organization constrains the regulatory interactions that govern vital cellular processes. Chromatin loops are key features of genome folding, yet it is unclear how genetic and epigenetic variation influences differential loop formation across individuals. Loops primarily form between two CTCF binding proteins, which recognize a specific motif at loop anchors. CTCF binding site motifs are frequently altered by base substitutions, structural variation, and 5-methylcytosine (m

Identifiers

PMID42282526
PMCPMC13252114

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.