Communications Biology (Oct 2022)

A multi-omic analysis of MCF10A cells provides a resource for integrative assessment of ligand-mediated molecular and phenotypic responses

  • 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

DOI
https://doi.org/10.1038/s42003-022-03975-9
Journal volume & issue
Vol. 5, no. 1
pp. 1 – 20

Abstract

Read online

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.