Evidence map›Paper›PMID 40399810›Full record

ArticleBMC bioinformatics2025

scHiCSRS: a self-representation smoothing method with Gaussian mixture model for imputing single cell Hi-C data.

Qing Xie, Wang Meng, Shili Lin

Abstract read
In one paragraph

Article in BMC bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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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

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Qing XieInterdisciplinary Ph.D. Program in Biostatistics, The Ohio State University, Columbus, OH, 43210, USA.
Wang MengAbigail Wexner Research Institute, Nationwide Children's Hospital, Columbus, OH, 43205, USA.
Shili LinInterdisciplinary Ph.D. Program in Biostatistics, The Ohio State University, Columbus, OH, 43210, USA. shili@stat.osu.edu.

Funding

Omics analysis of three-dimensional transcriptional regulationR01GM114142 · NIGMS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI JIN, VICTOR, LIN, SHILI · 2015 to 2024
$2.7M
NIGMS NIH HHS R01GM114142
6 · The paper itself

Abstract

backgroundSingle cell Hi-C (scHi-C) techniques make it possible to study cell-to-cell variability, but excess of zeros are makes scHi-C matrices extremely sparse and difficult for downstream analyses. The observed zeros are a combination of two events: structural zeros for which two loci never interact due to underlying biological mechanisms, or dropouts (sampling zeros) where two loci interact but not captured due to insufficient sequencing depth. Although data quality improvement approaches have been proposed, little has been done to differentiate these two types of zeros, even though such a distinction can greatly benefit downstream analysis such as clustering.

resultsWe propose scHiCSRS, a self-representation smoothing method that improves data quality, and a Gaussian mixture model that identifies structural zeros among observed zeros. scHiCSRS not only takes spatial dependencies of a scHi-C data matrix into account but also borrows information from similar single cells. Through an extensive set of simulation studies, we demonstrate the ability of scHiCSRS for identifying structural zeros with high sensitivity and for accurate imputation of dropout values in sampling zeros. Downstream analyses for three experimental datasets show that data improved from scHiCSRS yield more accurate clustering of cells than simply using observed data or improved data from comparison methods.

conclusionIn summary, scHiCSRS provides a valuable tool for identifying structural zeros and imputing dropouts. The resulted data are improved for downstream analysis, especially for understanding cell-to-cell variation through subtype clustering.

Indexed as

Single-Cell AnalysisSoftwareAlgorithmsHumansNormal DistributionDropoutsNeighborhoodsSampling zerosSparsityStructural zeros

Identifiers

PMID40399810
PMCPMC12093726

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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.