Evidence map›Paper›PMID 31178118›Full record

ArticleCell2019

Comprehensive Integration of Single-Cell Data.

Tim Stuart, Andrew Butler, Paul Hoffman, Christoph Hafemeister, Efthymia Papalexi, William M Mauck, Yuhan Hao, Marlon Stoeckius, Peter Smibert, Rahul Satija

Abstract read
In one paragraph

Article in Cell, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9,705 papers.

0numbers the graph read from it
0cells of the map it votes in
9,705citing 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

9,705 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Immunophenotyping by Single-Cell CITE-Seq.Methods in molecular biology (Clifton, N.J.) · 2027
    Article
  6. Article
  7. Article
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  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

9,645 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Tim StuartNew York Genome Center, New York, NY, USA.
Andrew ButlerNew York Genome Center, New York, NY, USA; Center for Genomics and Systems Biology, New York University, New York, NY, USA.
Paul HoffmanNew York Genome Center, New York, NY, USA.
Christoph HafemeisterNew York Genome Center, New York, NY, USA.
Efthymia PapalexiNew York Genome Center, New York, NY, USA; Center for Genomics and Systems Biology, New York University, New York, NY, USA.
William M MauckNew York Genome Center, New York, NY, USA; Center for Genomics and Systems Biology, New York University, New York, NY, USA.
Yuhan HaoNew York Genome Center, New York, NY, USA; Center for Genomics and Systems Biology, New York University, New York, NY, USA.
Marlon StoeckiusTechnology Innovation Lab, New York Genome Center, New York, NY, USA.
Peter SmibertTechnology Innovation Lab, New York Genome Center, New York, NY, USA.
Rahul SatijaNew York Genome Center, New York, NY, USA; Center for Genomics and Systems Biology, New York University, New York, NY, USA. Electronic address: rsatija@nygenome.org.

Funding

Regional and Genetic Diversity of Cortical InterneuronsR01MH071679 · NIMH · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI FISHELL, GORDON J · 2005 to 2020
$8.5M
Modeling Gene Regulatory Networks for Early Cardiopharyngeal DevelopmentR01HD096770 · NICHD · NEW YORK UNIVERSITY · PI BONNEAU, RICHARD A, CHRISTIAEN, LIONEL · 2018 to 2022
$3.0M
Comprehensive reference map construction, geolocation and data integration for HuBMAP HIVEOT2OD026673 · OD · NEW YORK GENOME CENTER · PI MARIONI, JOHN CARLO, SATIJA, RAHUL · 2018 to 2021
$2.9M
Learning the metadata of the cell with single cell genomicsDP2HG009623 · NHGRI · NEW YORK GENOME CENTER · PI SATIJA, RAHUL · 2016 to 2016
$2.8M
Massively Parallel Multi-Modal Single-Cell Phenotyping Using a Portable DeviceR21HG009748 · NHGRI · NEW YORK GENOME CENTER · PI SMIBERT, PETER · 2017 to 2019
$754k
The chromatin regulatory circuitry of bivalent domainsF32HD075541 · NICHD · BROAD INSTITUTE, INC. · PI SATIJA, RAHUL · 2013 to 2014
$99k
NHGRI NIH HHS DP2 HG009623NHGRI NIH HHS R21 HG009748NICHD NIH HHS F32 HD075541NICHD NIH HHS R01 HD096770NIH HHS OT2 OD026673NIMH NIH HHS R01 MH071679
6 · The paper itself

Abstract

Single-cell transcriptomics has transformed our ability to characterize cell states, but deep biological understanding requires more than a taxonomic listing of clusters. As new methods arise to measure distinct cellular modalities, a key analytical challenge is to integrate these datasets to better understand cellular identity and function. Here, we develop a strategy to "anchor" diverse datasets together, enabling us to integrate single-cell measurements not only across scRNA-seq technologies, but also across different modalities. After demonstrating improvement over existing methods for integrating scRNA-seq data, we anchor scRNA-seq experiments with scATAC-seq to explore chromatin differences in closely related interneuron subsets and project protein expression measurements onto a bone marrow atlas to characterize lymphocyte populations. Lastly, we harmonize in situ gene expression and scRNA-seq datasets, allowing transcriptome-wide imputation of spatial gene expression patterns. Our work presents a strategy for the assembly of harmonized references and transfer of information across datasets.

Indexed as

Databases, Nucleic AcidGene Expression ProfilingSequence Analysis, RNASingle-Cell AnalysisSoftwareTranscriptomeHumansintegrationmulti-modalscATAC-seqscRNA-seqsingle cellsingle-cell ATAC sequencingsingle-cell RNA sequencing

Identifiers

PMID31178118
PMCPMC6687398

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.