Evidence map›Paper›PMID 36071107›Full record

ArticleNature communications2022

devCellPy is a machine learning-enabled pipeline for automated annotation of complex multilayered single-cell transcriptomic data.

Francisco X Galdos, Sidra Xu, William R Goodyer, Lauren Duan, Yuhsin V Huang, Soah Lee, Han Zhu, Carissa Lee, Nicholas Wei, Daniel Lee and 1 more

Abstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing 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

27 citing papers in PubMed.

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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

11 authors.

Francisco X Galdos *Cardiovascular Institute, Stanford University School of Medicine, Stanford, CA, USA.ORCID 0000-0002-7985-4521
Sidra Xu *Cardiovascular Institute, Stanford University School of Medicine, Stanford, CA, USA.ORCID 0000-0002-7323-7557
William R GoodyerCardiovascular Institute, Stanford University School of Medicine, Stanford, CA, USA.
Lauren DuanCardiovascular Institute, Stanford University School of Medicine, Stanford, CA, USA.ORCID 0000-0002-0715-0824
Yuhsin V HuangCardiovascular Institute, Stanford University School of Medicine, Stanford, CA, USA.
Soah LeeBiopharmaceutical Convergence, School of Pharmacy, Sungkyunkwan University, Suwon, South Korea.
Han ZhuCardiovascular Institute, Stanford University School of Medicine, Stanford, CA, USA.ORCID 0000-0002-2751-7814
Carissa LeeCardiovascular Institute, Stanford University School of Medicine, Stanford, CA, USA.ORCID 0000-0003-1523-9770
Nicholas WeiCardiovascular Institute, Stanford University School of Medicine, Stanford, CA, USA.
Daniel LeeCardiovascular Institute, Stanford University School of Medicine, Stanford, CA, USA.
Sean M WuCardiovascular Institute, Stanford University School of Medicine, Stanford, CA, USA. smwu@stanford.edu.ORCID 0000-0002-0000-3821

Funding

From proteins to cells to tissues: A multi-scale assessment of biomechanical regulation by the myosin molecular motorRM1GM131981 · NIGMS · STANFORD UNIVERSITY · PI BERNSTEIN, DANIEL, MACK, DAVID LEE · 2019 to 2023
$10.3M
Enabling Technologies for Human-Machine Hybrid TissuesDP1LM012179 · NLM · STANFORD UNIVERSITY · PI WU, SEAN M · 2014 to 2018
$3.8M
Identification of Causal T-Cell Mechanisms in Immune Checkpoint Inhibitor Induced MyocarditisK08HL161405 · NHLBI · STANFORD UNIVERSITY · PI Han Zhu · 2022 to 2026
$880k
Understanding the Mechanisms of Ventricular Dysfunction in Hypoplastic Left Heart SyndromeF30HL149152 · NHLBI · STANFORD UNIVERSITY · PI GALDOS, FRANCISCO XAVIER · 2019 to 2021
$109k
NHLBI NIH HHS F30 HL149152NHLBI NIH HHS K08 HL161405NIGMS NIH HHS RM1 GM131981NLM NIH HHS DP1 LM012179
6 · The paper itself

Abstract

A major informatic challenge in single cell RNA-sequencing analysis is the precise annotation of datasets where cells exhibit complex multilayered identities or transitory states. Here, we present devCellPy a highly accurate and precise machine learning-enabled tool that enables automated prediction of cell types across complex annotation hierarchies. To demonstrate the power of devCellPy, we construct a murine cardiac developmental atlas from published datasets encompassing 104,199 cells from E6.5-E16.5 and train devCellPy to generate a cardiac prediction algorithm. Using this algorithm, we observe a high prediction accuracy (>90%) across multiple layers of annotation and across de novo murine developmental data. Furthermore, we conduct a cross-species prediction of cardiomyocyte subtypes from in vitro-derived human induced pluripotent stem cells and unexpectedly uncover a predominance of left ventricular (LV) identity that we confirmed by an LV-specific TBX5 lineage tracing system. Together, our results show devCellPy to be a useful tool for automated cell prediction across complex cellular hierarchies, species, and experimental systems.

Indexed as

Induced Pluripotent Stem CellsTranscriptomeAlgorithmsAnimalsHumansMachine LearningMiceMyocytes, Cardiac

Identifiers

PMID36071107
PMCPMC9452519

What OpenQuestion holds

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LicenceCC BY
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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.