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Three million images and morphological profiles of cells treated with matched chemical and genetic perturbations.
Chandrasekaran, Srinivas Niranj; Cimini, Beth A; Goodale, Amy; Miller, Lisa; Kost-Alimova, Maria; Jamali, Nasim; Doench, John G; Fritchman, Briana; Skepner, Adam; Melanson, Michelle; Kalinin, Alexandr A; Arevalo, John; Haghighi, Marzieh; Caicedo, Juan C; Kuhn, Daniel; Hernandez, Desiree; Berstler, James; Shafqat-Abbasi, Hamdah; Root, David E; Swalley, Susanne E; Garg, Sakshi; Singh, Shantanu; Carpenter, Anne E.
Affiliation
  • Chandrasekaran SN; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Cimini BA; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Goodale A; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Miller L; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Kost-Alimova M; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Jamali N; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Doench JG; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Fritchman B; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Skepner A; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Melanson M; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Kalinin AA; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Arevalo J; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Haghighi M; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Caicedo JC; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Kuhn D; Merck Healthcare KGaA, Darmstadt, Germany.
  • Hernandez D; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Berstler J; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Shafqat-Abbasi H; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Root DE; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Swalley SE; Biogen Inc., Cambridge, MA, USA.
  • Garg S; Merck Healthcare KGaA, Darmstadt, Germany.
  • Singh S; Broad Institute of MIT and Harvard, Cambridge, MA, USA. shantanu@broadinstitute.org.
  • Carpenter AE; Broad Institute of MIT and Harvard, Cambridge, MA, USA. anne@broadinstitute.org.
Nat Methods ; 21(6): 1114-1121, 2024 Jun.
Article in En | MEDLINE | ID: mdl-38594452
ABSTRACT
The identification of genetic and chemical perturbations with similar impacts on cell morphology can elucidate compounds' mechanisms of action or novel regulators of genetic pathways. Research on methods for identifying such similarities has lagged due to a lack of carefully designed and well-annotated image sets of cells treated with chemical and genetic perturbations. Here we create such a Resource dataset, CPJUMP1, in which each perturbed gene's product is a known target of at least two chemical compounds in the dataset. We systematically explore the directionality of correlations among perturbations that target the same protein encoded by a given gene, and we find that identifying matches between chemical and genetic perturbations is a challenging task. Our dataset and baseline analyses provide a benchmark for evaluating methods that measure perturbation similarities and impact, and more generally, learn effective representations of cellular state from microscopy images. Such advancements would accelerate the applications of image-based profiling of cellular states, such as uncovering drug mode of action or probing functional genomics.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Image Processing, Computer-Assisted Limits: Humans Language: En Journal: Nat Methods Journal subject: TECNICAS E PROCEDIMENTOS DE LABORATORIO Year: 2024 Document type: Article Affiliation country: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Image Processing, Computer-Assisted Limits: Humans Language: En Journal: Nat Methods Journal subject: TECNICAS E PROCEDIMENTOS DE LABORATORIO Year: 2024 Document type: Article Affiliation country: Estados Unidos