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Multidimensional Drug Profiling By Automated Microscopy
Zachary E. Perlman,1,2*Michael D. Slack,3*Yan Feng,1*Timothy J. Mitchison,1,2Lani F. Wu,3Steven J. Altschuler3
We present a method for high-throughput cytological profilingby microscopy. Our system provides quantitative multidimensionalmeasures of individual cell states over wide ranges of perturbations.We profile dose-dependent phenotypic effects of drugs in humancell culture with a titration-invariant similarity score (TISS).This method successfully categorized blinded drugs and suggestedtargets for drugs of uncertain mechanism. Multivariate single-cellanalysis is a starting point for identifying relationships amongdrug effects at a systems level and a step toward phenotypicprofiling at the single-cell level. Our methods will be usefulfor discovering the mechanism and predicting the toxicity ofnew drugs.
1 Institute of Chemistry and Cell Biology, Harvard Medical School, Boston, MA 02115, USA. 2 Department of Systems Biology, Harvard Medical School, Boston, MA 02115, USA. 3 Bauer Center for Genomics Research, Harvard University, Cambridge, MA 02138, USA.
* These authors contributed equally to this work.
Present address: Alphatech, Inc., San Diego, CA 92123, USA.
Present address: Novartis Institutes for BioMedical Research,Cambridge, MA 02139, USA.
To whom correspondence should be addressed. E-mail: saltschuler{at}cgr.harvard.edu (S.J.A.); lwu{at}cgr.harvard.edu (L.F.W.)
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