학술논문
A multi-omic analysis of MCF10A cells provides a resource for integrative assessment of ligand-mediated molecular and phenotypic responses
Document Type
article
Author
Sean M. Gross; Mark A. Dane; Rebecca L. Smith; Kaylyn L. Devlin; Ian C. McLean; Daniel S. Derrick; Caitlin E. Mills; Kartik Subramanian; Alexandra B. London; Denis Torre; John Erol Evangelista; Daniel J. B. Clarke; Zhuorui Xie; Cemal Erdem; Nicholas Lyons; Ted Natoli; Sarah Pessa; Xiaodong Lu; James Mullahoo; Jonathan Li; Miriam Adam; Brook Wassie; Moqing Liu; David F. Kilburn; Tiera A. Liby; Elmar Bucher; Crystal Sanchez-Aguila; Kenneth Daily; Larsson Omberg; Yunguan Wang; Connor Jacobson; Clarence Yapp; Mirra Chung; Dusica Vidovic; Yiling Lu; Stephan Schurer; Albert Lee; Ajay Pillai; Aravind Subramanian; Malvina Papanastasiou; Ernest Fraenkel; Heidi S. Feiler; Gordon B. Mills; Jake D. Jaffe; Avi Ma’ayan; Marc R. Birtwistle; Peter K. Sorger; James E. Korkola; Joe W. Gray; Laura M. Heiser
Source
Communications Biology, Vol 5, Iss 1, Pp 1-20 (2022)
Subject
Language
English
ISSN
2399-3642
Abstract
Comprehensive profiling of ligand-induced perturbation responses of the MCF10A mammary epithelial cell line provides an exhaustive resource for identification of the molecular basis of cellular phenotypes.