Evidence map›Paper›PMID 38940151›Full record

ArticleBioinformatics (Oxford, England)2024

scGrapHiC: deep learning-based graph deconvolution for Hi-C using single cell gene expression.

Ghulam Murtaza, Byron Butaney, Justin Wagner, Ritambhara Singh

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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 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Ghulam MurtazaDepartment of Computer Science, Brown University, 115 Waterman Street, Providence, RI, 02912, United States.ORCID 0000-0002-1803-1134
Byron ButaneyDepartment of Computer Science, Brown University, 115 Waterman Street, Providence, RI, 02912, United States.
Justin WagnerMaterial Measurement Laboratory, National Institute of Standards and Technology, Gaithersburg, MD, 20899, United States.
Ritambhara SinghDepartment of Computer Science, Brown University, 115 Waterman Street, Providence, RI, 02912, United States.ORCID 0000-0002-7523-160X

Funding

Deep learning for understanding gene regulation in diseases via 'omics' integrationR35HG011939 · NHGRI · BROWN UNIVERSITY · PI SINGH, RITAMBHARA · 2021 to 2025
$1.9M
NHGRI NIH HHS R35 HG011939NIH HHS 1R35HG011939-01
6 · The paper itself

Abstract

summarySingle-cell Hi-C (scHi-C) protocol helps identify cell-type-specific chromatin interactions and sheds light on cell differentiation and disease progression. Despite providing crucial insights, scHi-C data is often underutilized due to the high cost and the complexity of the experimental protocol. We present a deep learning framework, scGrapHiC, that predicts pseudo-bulk scHi-C contact maps using pseudo-bulk scRNA-seq data. Specifically, scGrapHiC performs graph deconvolution to extract genome-wide single-cell interactions from a bulk Hi-C contact map using scRNA-seq as a guiding signal. Our evaluations show that scGrapHiC, trained on seven cell-type co-assay datasets, outperforms typical sequence encoder approaches. For example, scGrapHiC achieves a substantial improvement of 23.2% in recovering cell-type-specific Topologically Associating Domains over the baselines. It also generalizes to unseen embryo and brain tissue samples. scGrapHiC is a novel method to generate cell-type-specific scHi-C contact maps using widely available genomic signals that enables the study of cell-type-specific chromatin interactions. AVAILABILITY AND IMPLEMENTATION: The GitHub link: https://github.com/rsinghlab/scGrapHiC contains the source code of scGrapHiC and associated scripts to preprocess publicly available datasets to produce the results and visualizations we have discuss in this manuscript.

Indexed as

ChromatinDeep LearningSingle-Cell AnalysisHumansChromatin

Identifiers

PMID38940151
PMCPMC11256916

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LicenceCC BY
Read underepoch 390

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.