Evidence map›Paper›PMID 31176620›Full record

ArticleCell systems2019

Geometric Sketching Compactly Summarizes the Single-Cell Transcriptomic Landscape.

Brian Hie, Hyunghoon Cho, Benjamin DeMeo, Bryan Bryson, Bonnie Berger

Abstract read
In one paragraph

Article in Cell systems, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 100 papers.

0numbers the graph read from it
0cells of the map it votes in
100citing 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

100 citing papers in PubMed.

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  16. Loss of lung mesenchymal identities in culture and a screening approach to identify restorative cues.American journal of physiology. Lung cellular and molecular physiology · 2025
    Article
  17. Article
  18. Article
  19. Review
  20. Article

40 more citing papers are in PubMed but not listed here.

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

5 authors.

Brian HieComputer Science and Artificial Intelligence Laboratory, MIT, Cambridge, MA 02139, USA.
Hyunghoon ChoComputer Science and Artificial Intelligence Laboratory, MIT, Cambridge, MA 02139, USA.
Benjamin DeMeoDepartment of Mathematics, MIT, Cambridge, MA 02139, USA; Department of Biomedical Informatics, Harvard University, Cambridge, MA 02138, USA.
Bryan BrysonDepartment of Biological Engineering, MIT, Cambridge, MA 02139, USA.
Bonnie BergerComputer Science and Artificial Intelligence Laboratory, MIT, Cambridge, MA 02139, USA; Department of Mathematics, MIT, Cambridge, MA 02139, USA. Electronic address: bab@mit.edu.

Funding

Training Program in Bioinformatics and Integrative GenomicsT32HG002295 · NHGRI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI Peter J Park · 2001 to 2026
$15.8M
Structure-Based Prediction of the InteractomeR01GM081871 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI BERGER, BONNIE · 2008 to 2020
$4.3M
Compressive genomics for large omics data sets: Algorithms applications & toolsR01GM108348 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI BERGER, BONNIE · 2013 to 2019
$2.1M
NHGRI NIH HHS T32 HG002295NIGMS NIH HHS R01 GM081871NIGMS NIH HHS R01 GM108348
6 · The paper itself

Abstract

Large-scale single-cell RNA sequencing (scRNA-seq) studies that profile hundreds of thousands of cells are becoming increasingly common, overwhelming existing analysis pipelines. Here, we describe how to enhance and accelerate single-cell data analysis by summarizing the transcriptomic heterogeneity within a dataset using a small subset of cells, which we refer to as a geometric sketch. Our sketches provide more comprehensive visualization of transcriptional diversity, capture rare cell types with high sensitivity, and reveal biological cell types via clustering. Our sketch of umbilical cord blood cells uncovers a rare subpopulation of inflammatory macrophages, which we experimentally validated. The construction of our sketches is extremely fast, which enabled us to accelerate other crucial resource-intensive tasks, such as scRNA-seq data integration, while maintaining accuracy. We anticipate our algorithm will become an increasingly essential step when sharing and analyzing the rapidly growing volume of scRNA-seq data and help enable the democratization of single-cell omics.

Indexed as

TranscriptomeAlgorithmsAnimalsData AnalysisDatasets as TopicGenetic HeterogeneityHumansMacrophagesRNA-SeqSingle-Cell Analysisbig datadata integrationdiversitygeometric sketchingheterogeneityrare cell-type discoverysamplingscRNA-seqsingle-cell RNA-seqsketching

Identifiers

PMID31176620
PMCPMC6597305

What OpenQuestion holds

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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.