Evidence map›Paper›PMID 33722077›Full record

ReviewAnnual review of genomics and human genetics2021

Applications of Single-Cell DNA Sequencing.

Gilad D Evrony, Anjali Gupta Hinch, Chongyuan Luo

Abstract readReview
In one paragraph

Review in Annual review of genomics and human genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing 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

65 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Evaluating the Utilities of Foundation Models in Single-Cell Data Analysis.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  7. Article
  8. Article
  9. Article
  10. Benchmarking Ploidy Estimation Methods for Bulk and Single-Cell Whole Genome Sequencing.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. scafari: exploring scDNA-seq data.Bioinformatics (Oxford, England) · 2025
    Article
  16. Review
  17. Article
  18. Review
  19. Review
  20. Review

5 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

3 authors.

Gilad D EvronyCenter for Human Genetics and Genomics, Grossman School of Medicine, New York University, New York, NY 10016, USA; email: gilad.evrony@nyulangone.org.
Anjali Gupta HinchWellcome Centre for Human Genetics, University of Oxford, Oxford OX3 7BN, United Kingdom; email: anjali@well.ox.ac.uk.
Chongyuan LuoDepartment of Human Genetics, University of California, Los Angeles, California 90095, USA; email: cluo@mednet.ucla.edu.

Funding

Single-cell genomic approaches to study the cellular origins of brain tumorsDP5OD028158 · OD · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI EVRONY, GILAD DAVID · 2019 to 2023
$2.1M
NIH HHS DP5 OD028158Wellcome TrustWellcome Trust 095552/Z/11/Z
6 · The paper itself

Abstract

Over the past decade, genomic analyses of single cells-the fundamental units of life-have become possible. Single-cell DNA sequencing has shed light on biological questions that were previously inaccessible across diverse fields of research, including somatic mutagenesis, organismal development, genome function, and microbiology. Single-cell DNA sequencing also promises significant future biomedical and clinical impact, spanning oncology, fertility, and beyond. While single-cell approaches that profile RNA and protein have greatly expanded our understanding of cellular diversity, many fundamental questions in biology and important biomedical applications require analysis of the DNA of single cells. Here, we review the applications and biological questions for which single-cell DNA sequencing is uniquely suited or required. We include a discussion of the fields that will be impacted by single-cell DNA sequencing as the technology continues to advance.

Indexed as

GenomeGenomicsDNAHumansRNASequence Analysis, DNADNARNADNA modificationsgerm cellslineage tracingorganismal developmentsingle-cell DNA sequencingsingle-cell genomics

Identifiers

PMID33722077
PMCPMC8410678

What OpenQuestion holds

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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.