Evidence map›Paper›PMID 36395727›Full record

ArticleCell systems2022

Morphology and gene expression profiling provide complementary information for mapping cell state.

Gregory P Way, Ted Natoli, Adeniyi Adeboye, Lev Litichevskiy, Andrew Yang, Xiaodong Lu, Juan C Caicedo, Beth A Cimini, Kyle Karhohs, David J Logan and 10 more

Abstract read
In one paragraph

Article in Cell systems, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 95 papers.

0numbers the graph read from it
0cells of the map it votes in
95citing 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

95 citing papers in PubMed.

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  20. Review

35 more citing papers are in PubMed but not listed here.

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

20 authors.

Gregory P WayImaging Platform, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA; Department of Biomedical Informatics, University of Colorado School of Medicine, Aurora, CO 80045, USA.
Ted NatoliCancer Program, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
Adeniyi AdeboyeImaging Platform, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
Lev LitichevskiyCancer Program, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
Andrew YangCancer Program, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
Xiaodong LuCancer Program, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
Juan C CaicedoImaging Platform, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
Beth A CiminiImaging Platform, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
Kyle KarhohsImaging Platform, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
David J LoganImaging Platform, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
Mohammad H RohbanImaging Platform, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
Maria Kost-AlimovaCenter for the Development of Therapeutics, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
Kate HartlandCenter for the Development of Therapeutics, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
Michael BornholdtImaging Platform, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
Srinivas Niranj ChandrasekaranImaging Platform, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
Marzieh HaghighiImaging Platform, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
Erin WeisbartImaging Platform, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
Shantanu SinghImaging Platform, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
Aravind SubramanianCancer Program, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA. Electronic address: asubramanian@dewpointx.com.
Anne E CarpenterImaging Platform, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA. Electronic address: anne@broadinstitute.org.

Funding

Extracting rich information from biological imagesR35GM122547 · NIGMS · BROAD INSTITUTE, INC. · PI Anne E. Carpenter · 2017 to 2026
$6.2M
H3Africa Kidney Disease Research NetworkU54HG006939 · NHGRI · NOGUCHI MEMORIAL INSTITUTE / MEDICAL RES · PI ADU, DWOMOA, OJO, AKINLOLU OLUSEUN · 2012 to 2017
$6.1M
LINCS Data Coordination and Integration CenterU01HG008699 · NHGRI · BROAD INSTITUTE, INC. · PI GOLUB, TODD R., SUBRAMANIAN, ARAVIND · 2015 to 2019
$3.2M
Opera Phenix high-throughput microplate confocal imager for high-content screeningS10OD026839 · OD · BROAD INSTITUTE, INC. · PI WAGNER, BRIDGET K · 2019 to 2019
$1.0M
NHGRI NIH HHS U01 HG008699NHGRI NIH HHS U54 HG006939NIGMS NIH HHS R35 GM122547NIH HHS S10 OD026839
6 · The paper itself

Abstract

Morphological and gene expression profiling can cost-effectively capture thousands of features in thousands of samples across perturbations by disease, mutation, or drug treatments, but it is unclear to what extent the two modalities capture overlapping versus complementary information. Here, using both the L1000 and Cell Painting assays to profile gene expression and cell morphology, respectively, we perturb human A549 lung cancer cells with 1,327 small molecules from the Drug Repurposing Hub across six doses, providing a data resource including dose-response data from both assays. The two assays capture both shared and complementary information for mapping cell state. Cell Painting profiles from compound perturbations are more reproducible and show more diversity but measure fewer distinct groups of features. Applying unsupervised and supervised methods to predict compound mechanisms of action (MOAs) and gene targets, we find that the two assays not only provide a partially shared but also a complementary view of drug mechanisms. Given the numerous applications of profiling in biology, our analyses provide guidance for planning experiments that profile cells for detecting distinct cell types, disease phenotypes, and response to chemical or genetic perturbations.

Indexed as

Gene Expression ProfilingHumansPhenotypebenchmarkCell Paintingdrug discoveryhigh-dimensional profilingimagesL1000systems biology

Identifiers

PMID36395727
PMCPMC10246468

What OpenQuestion holds

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LicenceTDM
Read underepoch 390

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.