Evidence map›Paper›PMID 37918402›Full record

ArticleCell reports methods2023

Accessible high-throughput single-cell whole-genome sequencing with paired chromatin accessibility.

Konstantin Queitsch, Travis W Moore, Brendan L O'Connell, Ruth V Nichols, John L Muschler, Dove Keith, Charles Lopez, Rosalie C Sears, Gordon B Mills, Galip Gürkan Yardımcı and 1 more

Abstract read
In one paragraph

Article in Cell reports methods, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
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  5. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Konstantin QueitschDepartment of Molecular & Medical Genetics, Oregon Health & Science University, Portland, OR, USA.
Travis W MooreCancer Early Detection Advanced Research Center, Oregon Health & Science University, Portland, OR, USA; Knight Cancer Institute, Oregon Health & Science University, Portland, OR, USA.
Brendan L O'ConnellDepartment of Molecular & Medical Genetics, Oregon Health & Science University, Portland, OR, USA; Cancer Early Detection Advanced Research Center, Oregon Health & Science University, Portland, OR, USA; Knight Cancer Institute, Oregon Health & Science University, Portland, OR, USA.
Ruth V NicholsDepartment of Molecular & Medical Genetics, Oregon Health & Science University, Portland, OR, USA.
John L MuschlerKnight Cancer Institute, Oregon Health & Science University, Portland, OR, USA; Department of Biomedical Engineering, Oregon Health & Science University, Portland, OR, USA; Brenden-Colson Center for Pancreatic Care, Oregon Health & Science University, Portland, OR, USA.
Dove KeithBrenden-Colson Center for Pancreatic Care, Oregon Health & Science University, Portland, OR, USA.
Charles LopezKnight Cancer Institute, Oregon Health & Science University, Portland, OR, USA.
Rosalie C SearsDepartment of Molecular & Medical Genetics, Oregon Health & Science University, Portland, OR, USA; Cancer Early Detection Advanced Research Center, Oregon Health & Science University, Portland, OR, USA; Knight Cancer Institute, Oregon Health & Science University, Portland, OR, USA; Brenden-Colson Center for Pancreatic Care, Oregon Health & Science University, Portland, OR, USA.
Gordon B MillsKnight Cancer Institute, Oregon Health & Science University, Portland, OR, USA; Department of Cell, Developmental and Cancer Biology, Oregon Health & Science University, Portland, OR, USA.
Galip Gürkan YardımcıCancer Early Detection Advanced Research Center, Oregon Health & Science University, Portland, OR, USA; Knight Cancer Institute, Oregon Health & Science University, Portland, OR, USA.
Andrew C AdeyDepartment of Molecular & Medical Genetics, Oregon Health & Science University, Portland, OR, USA; Cancer Early Detection Advanced Research Center, Oregon Health & Science University, Portland, OR, USA; Knight Cancer Institute, Oregon Health & Science University, Portland, OR, USA; Knight Cardiovascular Institute, Oregon Health & Science University, Portland, OR, USA. Electronic address: adey@ohsu.edu.

Funding

Program in Biomedical SciencesT32GM142619 · NIGMS · OREGON HEALTH & SCIENCE UNIVERSITY · PI Jeffrey Wallace Tyner · 2021 to 2026
$3.2M
Integrative characterization of cell state via modeling of multi-omics dataR35GM147698 · NIGMS · OREGON HEALTH & SCIENCE UNIVERSITY · PI Galip Gurkan Yardimci · 2022 to 2026
$1.9M
Accessible high-throughput single-cell genome sequencingR33CA269015 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI ADEY, ANDREW · 2022 to 2024
$1.1M
NCI NIH HHS R33 CA269015NIGMS NIH HHS R35 GM147698NIGMS NIH HHS T32 GM142619
6 · The paper itself

Abstract

Single-cell whole-genome sequencing (scWGS) enables the assessment of genome-level molecular differences between individual cells with particular relevance to genetically diverse systems like solid tumors. The application of scWGS was limited due to a dearth of accessible platforms capable of producing high-throughput profiles. We present a technique that leverages nucleosome disruption methodologies with the widely adopted 10× Genomics ATAC-seq workflow to produce scWGS profiles for high-throughput copy-number analysis without new equipment or custom reagents. We further demonstrate the use of commercially available indexed transposase complexes from ScaleBio for sample multiplexing, reducing the per-sample preparation costs. Finally, we demonstrate that sequential indexed tagmentation with an intervening nucleosome disruption step allows for the generation of both ATAC and WGS data from the same cell, producing comparable data to the unimodal assays. By exclusively utilizing accessible commercial reagents, we anticipate that these scWGS and scWGS+ATAC methods can be broadly adopted by the research community.

Indexed as

ChromatinNucleosomesGenomeHigh-Throughput Nucleotide SequencingSequence Analysis, DNAChromatinNucleosomescancer biologychromatin accessibilitycopy-number alterationsCP: BiotechnologyCP: Geneticssingle-cell genomics

Identifiers

PMID37918402
PMCPMC10694488

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.