Evidence map›Paper›PMID 35776722›Full record

ArticlePloS one2022

Single-cell specific and interpretable machine learning models for sparse scChIP-seq data imputation.

Steffen Albrecht, Tommaso Andreani, Miguel A Andrade-Navarro, Jean Fred Fontaine

Abstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

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

4 authors.

Steffen AlbrechtInstitute of Organismic and Molecular Evolution (iOME), Faculty of Biology, Johannes Gutenberg University Mainz, Mainz, Germany.ORCID 0000-0002-9765-4136
Tommaso AndreaniInstitute of Organismic and Molecular Evolution (iOME), Faculty of Biology, Johannes Gutenberg University Mainz, Mainz, Germany.
Miguel A Andrade-NavarroInstitute of Organismic and Molecular Evolution (iOME), Faculty of Biology, Johannes Gutenberg University Mainz, Mainz, Germany.
Jean Fred FontaineInstitute of Organismic and Molecular Evolution (iOME), Faculty of Biology, Johannes Gutenberg University Mainz, Mainz, Germany.ORCID 0000-0002-1101-4091

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

motivationSingle-cell Chromatin ImmunoPrecipitation DNA-Sequencing (scChIP-seq) analysis is challenging due to data sparsity. High degree of sparsity in biological high-throughput single-cell data is generally handled with imputation methods that complete the data, but specific methods for scChIP-seq are lacking. We present SIMPA, a scChIP-seq data imputation method leveraging predictive information within bulk data from the ENCODE project to impute missing protein-DNA interacting regions of target histone marks or transcription factors.

resultsImputations using machine learning models trained for each single cell, each ChIP protein target, and each genomic region accurately preserve cell type clustering and improve pathway-related gene identification on real human data. Results on bulk data simulating single cells show that the imputations are single-cell specific as the imputed profiles are closer to the simulated cell than to other cells related to the same ChIP protein target and the same cell type. Simulations also show that 100 input genomic regions are already enough to train single-cell specific models for the imputation of thousands of undetected regions. Furthermore, SIMPA enables the interpretation of machine learning models by revealing interaction sites of a given single cell that are most important for the imputation model trained for a specific genomic region. The corresponding feature importance values derived from promoter-interaction profiles of H3K4me3, an activating histone mark, highly correlate with co-expression of genes that are present within the cell-type specific pathways in 2 real human and mouse datasets. The SIMPA's interpretable imputation method allows users to gain a deep understanding of individual cells and, consequently, of sparse scChIP-seq datasets. AVAILABILITY AND IMPLEMENTATION: Our interpretable imputation algorithm was implemented in Python and is available at https://github.com/salbrec/SIMPA.

Indexed as

GenomicsMachine LearningAnimalsCluster AnalysisDNAMiceSequence Analysis, DNADNA

Identifiers

PMID35776722
PMCPMC9249201

What OpenQuestion holds

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LicenceCC BY
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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.