Evidence map›Paper›PMID 35869420›Full record

ArticleBMC bioinformatics2022

ccImpute: an accurate and scalable consensus clustering based algorithm to impute dropout events in the single-cell RNA-seq data.

Marcin Malec, Hasan Kurban, Mehmet Dalkilic

Abstract read
In one paragraph

Article in BMC bioinformatics, 2022. 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

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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

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. [Imputation method for dropout in single-cell transcriptome data].Sheng wu yi xue gong cheng xue za zhi = Journal of biomedical engineering = Shengwu yixue gongchengxue zazhi · 2023
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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Marcin Malec *Luddy School of Informatics, Computing, and Engineering, Indiana University Bloomington, 107 S Indiana Ave, Bloomington, 47404, USA. mamalec@indiana.edu.
Hasan Kurban *Luddy School of Informatics, Computing, and Engineering, Indiana University Bloomington, 107 S Indiana Ave, Bloomington, 47404, USA.
Mehmet Dalkilic *Luddy School of Informatics, Computing, and Engineering, Indiana University Bloomington, 107 S Indiana Ave, Bloomington, 47404, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn recent years, the introduction of single-cell RNA sequencing (scRNA-seq) has enabled the analysis of a cell's transcriptome at an unprecedented granularity and processing speed. The experimental outcome of applying this technology is a [Formula: see text] matrix containing aggregated mRNA expression counts of M genes and N cell samples. From this matrix, scientists can study how cell protein synthesis changes in response to various factors, for example, disease versus non-disease states in response to a treatment protocol. This technology's critical challenge is detecting and accurately recording lowly expressed genes. As a result, low expression levels tend to be missed and recorded as zero - an event known as dropout. This makes the lowly expressed genes indistinguishable from true zero expression and different than the low expression present in cells of the same type. This issue makes any subsequent downstream analysis difficult.

resultsTo address this problem, we propose an approach to measure cell similarity using consensus clustering and demonstrate an effective and efficient algorithm that takes advantage of this new similarity measure to impute the most probable dropout events in the scRNA-seq datasets. We demonstrate that our approach exceeds the performance of existing imputation approaches while introducing the least amount of new noise as measured by clustering performance characteristics on datasets with known cell identities.

conclusionsccImpute is an effective algorithm to correct for dropout events and thus improve downstream analysis of scRNA-seq data. ccImpute is implemented in R and is available at https://github.com/khazum/ccImpute .

Indexed as

Single-Cell AnalysisSoftwareAlgorithmsCluster AnalysisConsensusGene Expression ProfilingRNA-SeqSequence Analysis, RNADownstream analysisDropout eventImputationNext generation sequencingscRNASingle-cell

Identifiers

PMID35869420
PMCPMC9306045

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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.