Evidence map›Paper›PMID 35338121›Full record

ArticleNature communications2022

Integrating deep learning and unbiased automated high-content screening to identify complex disease signatures in human fibroblasts.

Lauren Schiff, Bianca Migliori, Ye Chen, Deidre Carter, Caitlyn Bonilla, Jenna Hall, Minjie Fan, Edmund Tam, Sara Ahadi, Brodie Fischbacher and 33 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 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing 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

33 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

43 authors.

Lauren Schiff *Google Research, Mountain View, CA, USA.
Bianca Migliori *The New York Stem Cell Foundation Research Institute, New York, NY, USA.
Ye Chen *Google Research, Mountain View, CA, USA.
Deidre Carter *The New York Stem Cell Foundation Research Institute, New York, NY, USA.
Caitlyn BonillaGoogle Research, Mountain View, CA, USA.
Jenna HallThe New York Stem Cell Foundation Research Institute, New York, NY, USA.ORCID 0000-0003-4540-7798
Minjie FanGoogle Research, Mountain View, CA, USA.
Edmund TamThe New York Stem Cell Foundation Research Institute, New York, NY, USA.
Sara AhadiGoogle Research, Mountain View, CA, USA.
Brodie FischbacherThe New York Stem Cell Foundation Research Institute, New York, NY, USA.ORCID 0000-0002-6276-7149
Anton GeraschenkoGoogle Research, Mountain View, CA, USA.
Christopher J HunterThe New York Stem Cell Foundation Research Institute, New York, NY, USA.
Subhashini VenugopalanGoogle Research, Mountain View, CA, USA.ORCID 0000-0003-3729-8456
Sean DesMarteauThe New York Stem Cell Foundation Research Institute, New York, NY, USA.
Arunachalam NarayanaswamyGoogle Research, Mountain View, CA, USA.
Selwyn JacobThe New York Stem Cell Foundation Research Institute, New York, NY, USA.
Zan ArmstrongGoogle Research, Mountain View, CA, USA.ORCID 0000-0001-5231-7470
Peter FerrarottoThe New York Stem Cell Foundation Research Institute, New York, NY, USA.
Brian WilliamsGoogle Research, Mountain View, CA, USA.ORCID 0000-0002-2839-0106
Geoff Buckley-HerdThe New York Stem Cell Foundation Research Institute, New York, NY, USA.
Jon HazardGoogle Research, Mountain View, CA, USA.
Jordan GoldbergThe New York Stem Cell Foundation Research Institute, New York, NY, USA.
Marc CoramGoogle Research, Mountain View, CA, USA.ORCID 0000-0002-8877-2501
Reid OttoThe New York Stem Cell Foundation Research Institute, New York, NY, USA.
Edward A BaltzGoogle Research, Mountain View, CA, USA.
Laura Andres-MartinThe New York Stem Cell Foundation Research Institute, New York, NY, USA.
Orion PritchardGoogle Research, Mountain View, CA, USA.
Alyssa Duren-LubanskiThe New York Stem Cell Foundation Research Institute, New York, NY, USA.
Ameya DaigavaneGoogle Research, Mountain View, CA, USA.ORCID 0000-0002-5116-3075
Kathryn ReggioThe New York Stem Cell Foundation Research Institute, New York, NY, USA.
NYSCF Global Stem Cell Array® Team
Phillip C NelsonGoogle Research, Mountain View, CA, USA.
Michael FrumkinGoogle Research, Mountain View, CA, USA.
Susan L SolomonThe New York Stem Cell Foundation Research Institute, New York, NY, USA.
Lauren BauerThe New York Stem Cell Foundation Research Institute, New York, NY, USA.
Raeka S AiyarThe New York Stem Cell Foundation Research Institute, New York, NY, USA.
Elizabeth SchwarzbachThe New York Stem Cell Foundation Research Institute, New York, NY, USA.
Scott A NoggleThe New York Stem Cell Foundation Research Institute, New York, NY, USA.
Frederick J MonsmaThe New York Stem Cell Foundation Research Institute, New York, NY, USA.
Daniel PaullThe New York Stem Cell Foundation Research Institute, New York, NY, USA.ORCID 0000-0002-9004-794X
Marc BerndlGoogle Research, Mountain View, CA, USA. marcberndl@google.com.ORCID 0000-0001-6750-5861
Samuel J YangGoogle Research, Mountain View, CA, USA. samuely@google.com.ORCID 0000-0003-2460-6456
Bjarki JohannessonThe New York Stem Cell Foundation Research Institute, New York, NY, USA. johannesson.bjarki@gmail.com.ORCID 0000-0003-4756-0059

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Drug discovery for diseases such as Parkinson's disease are impeded by the lack of screenable cellular phenotypes. We present an unbiased phenotypic profiling platform that combines automated cell culture, high-content imaging, Cell Painting, and deep learning. We applied this platform to primary fibroblasts from 91 Parkinson's disease patients and matched healthy controls, creating the largest publicly available Cell Painting image dataset to date at 48 terabytes. We use fixed weights from a convolutional deep neural network trained on ImageNet to generate deep embeddings from each image and train machine learning models to detect morphological disease phenotypes. Our platform's robustness and sensitivity allow the detection of individual-specific variation with high fidelity across batches and plate layouts. Lastly, our models confidently separate LRRK2 and sporadic Parkinson's disease lines from healthy controls (receiver operating characteristic area under curve 0.79 (0.08 standard deviation)), supporting the capacity of this platform for complex disease modeling and drug screening applications.

Indexed as

Deep LearningParkinson DiseaseFibroblastsHumansMachine LearningNeural Networks, Computer

Identifiers

PMID35338121
PMCPMC8956598

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.