Automatic Identification of Subcellular Phenotypes on Human Cell Arrays
Author(s) -
Christian Conrad,
Holger Erfle,
Patrick Warnat,
Nathalie Daigle,
Thomas Lörch,
Jan Ellenberg,
Rainer Pepperkok,
Roland Eils
Publication year - 2004
Publication title -
genome research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.556
H-Index - 297
eISSN - 1549-5469
pISSN - 1088-9051
DOI - 10.1101/gr.2383804
Subject(s) - biology , phenotype , high content screening , subcellular localization , protein subcellular localization prediction , cell , proteome , microbiology and biotechnology , transfection , computational biology , cell type , high throughput screening , rna interference , functional genomics , genetic screen , hek 293 cells , phenotypic screening , cell culture , gene , genomics , bioinformatics , genetics , cytoplasm , genome , rna
Light microscopic analysis of cell morphology provides a high-content readout of cell function and protein localization. Cell arrays and microwell transfection assays on cultured cells have made cell phenotype analysis accessible to high-throughput experiments. Both the localization of each protein in the proteome and the effect of RNAi knock-down of individual genes on cell morphology can be assayed by manual inspection of microscopic images. However, the use of morphological readouts for functional genomics requires fast and automatic identification of complex cellular phenotypes. Here, we present a fully automated platform for high-throughput cell phenotype screening combining human live cell arrays, screening microscopy, and machine-learning-based classification methods. Efficiency of this platform is demonstrated by classification of eleven subcellular patterns marked by GFP-tagged proteins. Our classification method can be adapted to virtually any microscopic assay based on cell morphology, opening a wide range of applications including large-scale RNAi screening in human cells.
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