Evidence map›Paper›PMID 28679385›Full record

ArticleBMC biology2017

Q&A: using Patch-seq to profile single cells.

Cathryn R Cadwell, Rickard Sandberg, Xiaolong Jiang, Andreas S Tolias

Abstract read
In one paragraph

Article in BMC biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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 citing papers in PubMed.

  1. Review
  2. Review
  3. Patch-seq: Advances and Biological Applications.Cellular and molecular neurobiology · 2023
    Review
  4. Differential expression of GABAFrontiers in cellular neuroscience · 2023
    Article
  5. Article
  6. Review
  7. Article
  8. Assessing Transcriptome Quality in Patch-Seq Datasets.Frontiers in molecular neuroscience · 2018
    Article
  9. Article
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

4 authors.

Cathryn R CadwellDepartment of Neuroscience, Baylor College of Medicine, One Baylor Plaza, Houston, Texas, 77030, USA.
Rickard SandbergLudwig Institute for Cancer Research, Stockholm, Sweden.
Xiaolong JiangDepartment of Neuroscience, Baylor College of Medicine, One Baylor Plaza, Houston, Texas, 77030, USA.
Andreas S ToliasDepartment of Neuroscience, Baylor College of Medicine, One Baylor Plaza, Houston, Texas, 77030, USA. astolias@bcm.edu.

Funding

VISION RESEARCH CENTERP30EY002520 · NEI · BAYLOR COLLEGE OF MEDICINE · PI Samuel M Wu · 1985 to 2026
$14.8M
A MOLECULAR CODE FOR CONNECTIVITY IN THE NEOCORTEXR01MH103108 · NIMH · BAYLOR COLLEGE OF MEDICINE · PI TOLIAS, ANDREAS, TOLIAS, KIMBERLY R · 2013 to 2016
$1.3M
NEI NIH HHS P30 EY002520NIMH NIH HHS R01 MH103108
6 · The paper itself

Abstract

Individual neurons vary widely in terms of their gene expression, morphology, and electrophysiological properties. While many techniques exist to study single-cell variability along one or two of these dimensions, very few techniques can assess all three features for a single cell. We recently developed Patch-seq, which combines whole-cell patch clamp recording with single-cell RNA-sequencing and immunohistochemistry to comprehensively profile the transcriptomic, morphologic, and physiologic features of individual neurons. Patch-seq can be broadly applied to characterize cell types in complex tissues such as the nervous system, and to study the transcriptional signatures underlying the multidimensional phenotypes of single cells.

Indexed as

Patch-Clamp TechniquesSequence Analysis, RNATranscriptomeAnimalsElectrophysiological PhenomenaHumansImmunohistochemistryNeuronsSingle-Cell Analysis

Identifiers

PMID28679385
PMCPMC5499043

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Registered trials

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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.