Evidence map›Paper›PMID 31601804›Full record

ArticleNature communications2019

DC3 is a method for deconvolution and coupled clustering from bulk and single-cell genomics data.

Wanwen Zeng, Xi Chen, Zhana Duren, Yong Wang, Rui Jiang, Wing Hung Wong

Abstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

43 citing papers in PubMed.

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  16. GLUE multimodal single cell data.Precision clinical medicine · 2023
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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

6 authors.

Wanwen ZengDepartment of Statistics, Department of Biomedical Data Science, Bio-X Program, Stanford University, Stanford, CA, 94305, USA.
Xi ChenDepartment of Statistics, Department of Biomedical Data Science, Bio-X Program, Stanford University, Stanford, CA, 94305, USA.
Zhana DurenDepartment of Statistics, Department of Biomedical Data Science, Bio-X Program, Stanford University, Stanford, CA, 94305, USA.
Yong WangCEMS, NCMIS, MDIS, Academy of Mathematics and Systems Science, Chinese Academy of Sciences, Beijing, 100080, China.
Rui JiangMOE Key Laboratory of Bioinformatics, Bioinformatics Division, Department of Automation, Beijing National Research Center for Information Science and Technology, Tsinghua University, Beijing, 100084, China. ruijiang@tsinghua.edu.cn.
Wing Hung WongDepartment of Statistics, Department of Biomedical Data Science, Bio-X Program, Stanford University, Stanford, CA, 94305, USA. whwong@stanford.edu.

Funding

Special EquipmentP50HG007735 · NHGRI · STANFORD UNIVERSITY · PI CHANG, HOWARD Y · 2014 to 2018
$15.2M
Statistical methods for gene regulatory analysis and single cell genomicsR01HG010359 · NHGRI · STANFORD UNIVERSITY · PI WONG, WING H. · 2019 to 2022
$1.5M
Multivariate statistical methods, flow cytometry, and network modeling.R01GM109836 · NIGMS · STANFORD UNIVERSITY · PI WONG, WING H. · 2014 to 2017
$1.2M
NHGRI NIH HHS P50 HG007735NHGRI NIH HHS R01 HG010359NIGMS NIH HHS R01 GM109836
6 · The paper itself

Abstract

Characterizing and interpreting heterogeneous mixtures at the cellular level is a critical problem in genomics. Single-cell assays offer an opportunity to resolve cellular level heterogeneity, e.g., scRNA-seq enables single-cell expression profiling, and scATAC-seq identifies active regulatory elements. Furthermore, while scHi-C can measure the chromatin contacts (i.e., loops) between active regulatory elements to target genes in single cells, bulk HiChIP can measure such contacts in a higher resolution. In this work, we introduce DC3 (De-Convolution and Coupled-Clustering) as a method for the joint analysis of various bulk and single-cell data such as HiChIP, RNA-seq and ATAC-seq from the same heterogeneous cell population. DC3 can simultaneously identify distinct subpopulations, assign single cells to the subpopulations (i.e., clustering) and de-convolve the bulk data into subpopulation-specific data. The subpopulation-specific profiles of gene expression, chromatin accessibility and enhancer-promoter contact obtained by DC3 provide a comprehensive characterization of the gene regulatory system in each subpopulation.

Indexed as

AlgorithmsCluster AnalysisAnimalsCell LineChromatinChromatin ImmunoprecipitationComputer SimulationGene Expression ProfilingGene Regulatory NetworksGenomicsHigh-Throughput Nucleotide SequencingHumansMicePromoter Regions, GeneticSingle-Cell AnalysisChromatin

Identifiers

PMID31601804
PMCPMC6787340

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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.