Evidence map›Paper›PMID 26047807›Full record

ArticleGenome biology2015

Scalable microfluidics for single-cell RNA printing and sequencing.

Sayantan Bose, Zhenmao Wan, Ambrose Carr, Abbas H Rizvi, Gregory Vieira, Dana Pe'er, Peter A Sims

Abstract read
In one paragraph

Article in Genome biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 81 papers.

0numbers the graph read from it
0cells of the map it votes in
81citing 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

81 citing papers in PubMed.

  1. Article
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  14. On-chip dielectrophoretic single-cell manipulation.Microsystems & nanoengineering · 2024
    Review
  15. Article
  16. Article
  17. Article
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21 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Sayantan BoseDepartment of Systems Biology, Columbia University Medical Center, New York, NY, 10032, USA. sb3438@columbia.edu.
Zhenmao WanDepartment of Biological Sciences, Columbia University, New York, NY, 10027, USA. wanzhenmao@gmail.com.
Ambrose CarrDepartment of Biological Sciences, Columbia University, New York, NY, 10027, USA. ambrosejcarr@gmail.com.
Abbas H RizviDepartment of Biochemistry & Molecular Biophysics, Columbia University Medical Center, New York, NY, 10032, USA. abbas.rizvi@gmail.com.
Gregory VieiraDepartment of Systems Biology, Columbia University Medical Center, New York, NY, 10032, USA. gregorybv@gmail.com.
Dana Pe'erDepartment of Systems Biology, Columbia University Medical Center, New York, NY, 10032, USA. dpeer@biology.columbia.edu.
Peter A SimsDepartment of Systems Biology, Columbia University Medical Center, New York, NY, 10032, USA. pas2182@columbia.edu.

Funding

Topology of Cancer Evolution and HeterogeneityU54CA193313 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI IAVARONE, ANTONIO, RABADAN, RAUL · 2015 to 2020
$10.4M
Single cell mapping of developmental trajectories underlying health and diseaseDP1HD084071 · NICHD · SLOAN-KETTERING INST CAN RESEARCH · PI PE'ER, DANA · 2014 to 2018
$4.2M
A Microfluidic System for Image-Guided RNA-Seq of Single Cells in GlioblastomaK01EB016071 · NIBIB · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI SIMS, PETER ALAN · 2012 to 2016
$863k
Multiplexed, Single Molecule Protein Identification for Single Cell ProteomicsR21EB016980 · NIBIB · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI SIMS, PETER ALAN · 2012 to 2013
$413k
NCCDPHP CDC HHS DP1HD084071NCI NIH HHS U54 CA193313NIBIB NIH HHS K01 EB016071NIBIB NIH HHS K01EB016071NIBIB NIH HHS R21 EB016980NIBIB NIH HHS R21EB016980NICHD NIH HHS DP1 HD084071
6 · The paper itself

Abstract

Many important biological questions demand single-cell transcriptomics on a large scale. Hence, new tools are urgently needed for efficient, inexpensive manipulation of RNA from individual cells. We report a simple platform for trapping single-cell lysates in sealed, picoliter microwells capable of printing RNA on glass or capturing RNA on beads. We then develop a scalable technology for genome-wide, single-cell RNA-Seq. Our device generates pooled libraries from hundreds of individual cells with consumable costs of $0.10-$0.20 per cell and includes five lanes for simultaneous experiments. We anticipate that this system will serve as a general platform for single-cell imaging and sequencing.

Indexed as

Cell Line, TumorDimethylpolysiloxanesGene Expression ProfilingHigh-Throughput Nucleotide SequencingHumansMicrofluidic Analytical TechniquesOptical ImagingRNASequence Analysis, RNASingle-Cell AnalysisbaysilonDimethylpolysiloxanesRNA

Identifiers

PMID26047807
PMCPMC4487847

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.