Evidence map›Paper›PMID 32527285›Full record

ArticleBMC bioinformatics2020

A flexible network-based imputing-and-fusing approach towards the identification of cell types from single-cell RNA-seq data.

Yang Qi, Yang Guo, Huixin Jiao, Xuequn Shang

Abstract read
In one paragraph

Article in BMC bioinformatics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. MGPT: A Multi-task Graph Prompt Learning Framework for Drug Discovery.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  2. Article
  3. Single-Cell Analysis of the Transcriptome and Epigenome.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Yang QiSchool of Computer Science, Northwestern Polytechnical University, Xi'an, 710072, China.
Yang GuoSchool of Computer Science, Northwestern Polytechnical University, Xi'an, 710072, China. gyang@mail.nwpu.edu.cn.
Huixin JiaoSchool of Computer Science, Northwestern Polytechnical University, Xi'an, 710072, China.
Xuequn ShangSchool of Computer Science, Northwestern Polytechnical University, Xi'an, 710072, China. shang@nwpu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSingle-cell RNA sequencing (scRNA-seq) provides an effective tool to investigate the transcriptomic characteristics at the single-cell resolution. Due to the low amounts of transcripts in single cells and the technical biases in experiments, the raw scRNA-seq data usually includes large noise and makes the downstream analyses complicated. Although many methods have been proposed to impute the noisy scRNA-seq data in recent years, few of them take into account the prior associations across genes in imputation and integrate multiple types of imputation data to identify cell types.

resultsWe present a new framework, NetImpute, towards the identification of cell types from scRNA-seq data by integrating multiple types of biological networks. We employ a statistic method to detect the noise data items in scRNA-seq data and develop a new imputation model to estimate the real values of data noise by integrating the PPI network and gene pathways. Meanwhile, based on the data imputed by multiple types of biological networks, we propose an integrated approach to identify cell types from scRNA-seq data. Comprehensive experiments demonstrate that the proposed network-based imputation model can estimate the real values of noise data items accurately and integrating the imputation data based on multiple types of biological networks can improve the identification of cell types from scRNA-seq data.

conclusionsIncorporating the prior gene associations in biological networks can potentially help to improve the imputation of noisy scRNA-seq data and integrating multiple types of network-based imputation data can enhance the identification of cell types. The proposed NetImpute provides an open framework for incorporating multiple types of biological network data to identify cell types from scRNA-seq data.

Indexed as

HumansSequence Analysis, RNASingle-Cell AnalysisBiological networksCell typesData integrationDropout eventsscRNA-seq

Identifiers

PMID32527285
PMCPMC7291547

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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.