Evidence map›Paper›PMID 40585301›Full record

ArticleNAR genomics and bioinformatics2025

Charm is a flexible pipeline to simulate chromosomal rearrangements on Hi-C-like data.

Miroslav Nuriddinov, Polina Belokopytova, Veniamin Fishman

Abstract read
In one paragraph

Article in NAR genomics and bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
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

3 authors.

Miroslav NuriddinovInstitute of Cytology and Genetics (ICG), Novosibirsk 630099, Russia.ORCID https://orcid.org/0000-0002-2417-8263
Polina BelokopytovaInstitute of Cytology and Genetics (ICG), Novosibirsk 630099, Russia.
Veniamin FishmanInstitute of Cytology and Genetics (ICG), Novosibirsk 630099, Russia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Identifying structural variants (SVs) remains a pivotal challenge within genomic studies. The recent advent of chromosome conformation capture (3C) techniques has emerged as a promising avenue for the accurate identification of SVs. However, development and validation of computational methods leveraging 3C data necessitate comprehensive datasets of well-characterized chromosomal rearrangements, which are presently lacking. In this study, we introduce Charm (https://github.com/genomech/Charm): a robust computational framework tailored for Hi-C data simulation. Our findings demonstrate Charm's efficacy in benchmarking both novel and established tools for SV detection. Additionally, we furnish an extensive dataset of simulated Hi-C maps, paving the way for subsequent benchmarking endeavors.

Indexed as

GenomicsGenomic Structural VariationSoftwareChromosomesComputer SimulationHumans

Identifiers

PMID40585301
PMCPMC12204402

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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.