Evidence map›Paper›PMID 38940142›Full record

ArticleBioinformatics (Oxford, England)2024

Enhancing Hi-C contact matrices for loop detection with Capricorn: a multiview diffusion model.

Tangqi Fang, Yifeng Liu, Addie Woicik, Minsi Lu, Anupama Jha, Xiao Wang, Gang Li, Borislav Hristov, Zixuan Liu, Hanwen Xu and 2 more

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

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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

12 authors.

Tangqi FangPaul G. Allen School of Computer Science and Engineering, University of Washington, Seattle, WA 98195, United States.
Yifeng LiuPaul G. Allen School of Computer Science and Engineering, University of Washington, Seattle, WA 98195, United States.
Addie WoicikPaul G. Allen School of Computer Science and Engineering, University of Washington, Seattle, WA 98195, United States.
Minsi LuPaul G. Allen School of Computer Science and Engineering, University of Washington, Seattle, WA 98195, United States.
Anupama JhaDepartment of Genome Sciences, University of Washington, Seattle, WA 98195, United States.ORCID 0000-0003-3029-2086
Xiao WangDepartment of Computer Science, Purdue University, West Lafayette, IN 47907, United States.
Gang LiDepartment of Genome Sciences, University of Washington, Seattle, WA 98195, United States.
Borislav HristovDepartment of Genome Sciences, University of Washington, Seattle, WA 98195, United States.
Zixuan LiuPaul G. Allen School of Computer Science and Engineering, University of Washington, Seattle, WA 98195, United States.
Hanwen XuPaul G. Allen School of Computer Science and Engineering, University of Washington, Seattle, WA 98195, United States.
William S NoblePaul G. Allen School of Computer Science and Engineering, University of Washington, Seattle, WA 98195, United States.
Sheng WangPaul G. Allen School of Computer Science and Engineering, University of Washington, Seattle, WA 98195, United States.

Funding

Deep tensor genomic imputationR01HG011466 · NHGRI · UNIVERSITY OF WASHINGTON · PI NOBLE, WILLIAM STAFFORD · 2021 to 2024
$1.5M
NHGRI NIH HHS R01 HG011466NHGRI NIH HHS UM1 HG011531NIH HHS R01HG011466Sony Faculty Research Award
6 · The paper itself

Abstract

motivationHigh-resolution Hi-C contact matrices reveal the detailed three-dimensional architecture of the genome, but high-coverage experimental Hi-C data are expensive to generate. Simultaneously, chromatin structure analyses struggle with extremely sparse contact matrices. To address this problem, computational methods to enhance low-coverage contact matrices have been developed, but existing methods are largely based on resolution enhancement methods for natural images and hence often employ models that do not distinguish between biologically meaningful contacts, such as loops and other stochastic contacts.

resultsWe present Capricorn, a machine learning model for Hi-C resolution enhancement that incorporates small-scale chromatin features as additional views of the input Hi-C contact matrix and leverages a diffusion probability model backbone to generate a high-coverage matrix. We show that Capricorn outperforms the state of the art in a cross-cell-line setting, improving on existing methods by 17% in mean squared error and 26% in F1 score for chromatin loop identification from the generated high-coverage data. We also demonstrate that Capricorn performs well in the cross-chromosome setting and cross-chromosome, cross-cell-line setting, improving the downstream loop F1 score by 14% relative to existing methods. We further show that our multiview idea can also be used to improve several existing methods, HiCARN and HiCNN, indicating the wide applicability of this approach. Finally, we use DNA sequence to validate discovered loops and find that the fraction of CTCF-supported loops from Capricorn is similar to those identified from the high-coverage data. Capricorn is a powerful Hi-C resolution enhancement method that enables scientists to find chromatin features that cannot be identified in the low-coverage contact matrix. AVAILABILITY AND IMPLEMENTATION: Implementation of Capricorn and source code for reproducing all figures in this paper are available at https://github.com/CHNFTQ/Capricorn.

Indexed as

ChromatinMachine LearningAlgorithmsComputational BiologyHumansSoftwareChromatin

Identifiers

PMID38940142
PMCPMC11211821

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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.