Leveraging base-pair mammalian constraint to understand genetic variation and human disease
Patrick F. Sullivan(University of North Carolina at Chapel Hill), Mark Diekhans(University of California, Santa Cruz), Graham M. Hughes(University College Dublin), Katherine S. Pollard(QB3), Laura M. Huckins(Allen Institute for Brain Science), Sharadha Sakthikumar(Translational Genomics Research Institute), Matteo Bianchi(Uppsala University), Jin Szatkiewicz(Broad Institute), Michael X. Dong, Susan J. Birren(Brandeis University), Kevin R. Bredemeyer(Texas A&M University System), Shuyang Yao(Karolinska Institutet), Jia Wen(University of North Carolina at Chapel Hill), Ananya Roy(Uppsala University), Jian Zeng(The University of Queensland), James R. Xue(Howard Hughes Medical Institute), Steven Gazal(University of Southern California), Voichita D. Marinescu(Science for Life Laboratory), Jennifer R. S. Meadows(University of North Carolina at Chapel Hill), Matthew J. Christmas, Diane P. Genereux(Broad Institute), Zhili Zheng(Broad Institute), Quan Sun(University of North Carolina at Chapel Hill), Jiawen Chen(University of North Carolina at Chapel Hill), Ana M. Breit(Stony Brook University), Karin Forsberg‐Nilsson(Uppsala University), Benedict Paten(University of California, Santa Cruz), Naomi R. Wray(The University of Queensland), Ola Wallerman(Uppsala University), Steven K. Reilly(Yale University), Alyssa J. Lawler(Broad Institute), BaDoi N. Phan(University of Pittsburgh Medical Center), Hiram Clawson(University of California, Santa Cruz), Joana Damas(Bio-Medical Science (South Korea)), Zhiping Weng(UMass Memorial Health Care), Kathleen C. Keough(Personalis (United States)), Jessica Johnson(University of North Carolina at Chapel Hill), Yun Li(Shanghai University of Traditional Chinese Medicine), Xue Li(Broad Institute), Jessika Nordin(Science for Life Laboratory), Federica Di Palma(Italian Institute of Technology), Joel Armstrong(University of California, Santa Cruz)
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