PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data (original) (raw)

6 The AGRE Consortium: Dan Geschwind, UCLA, Los Angeles, CA; Maja Bucan, University of Pennsylvania, Philadelphia, PA; W. Ted Brown, N.Y.S. Institute for Basic Research in Developmental Disabilities, Staten Island, NY; Rita M. Cantor, UCLA School of Medicine, Los Angeles, CA; John N. Constantino, Washington University School of Medicine, St. Louis, MO; T. Conrad Gilliam, University of Chicago, Chicago, IL; Martha Herbert, Harvard Medical School, Boston, MA; Clara Lajonchere, Cure Autism Now/Autism Speaks, Los Angeles, CA; David H. Ledbetter, Emory University, Atlanta, GA; Christa Lese-Martin, Emory University, Atlanta, GA; Janet Miller, Cure Autism Now/Autism Speaks, Los Angeles, CA; Stanley F. Nelson, UCLA School of Medicine, Los Angeles, CA; Gerard D. Schellenberg, University of Washington, Seattle, WA; Carol A. Samango-Sprouse, George Washington University, Washington, DC; Sarah Spence, UCLA, Los Angeles, CA; Matthew State, Yale University, New Haven, CT; Rudolph E. Tanzi, Massachusetts General Hospital, Boston, MA.