机译:临床测序循证事项研究联盟:在多种和医学欠缺的人群中整合基因组测序
Division of Medical Genetics Department of Medicine University of Washington;
Department of Genetics University of North Carolina at Chapel Hill;
Center for Health Equity and Community Engaged Research Icahn School of Medicine at Mount Sinai;
Division of Medical Genetics Department of Medicine University of Washington;
Department of Epidemiology University of North Carolina at Chapel Hill;
Research Triangle Institute International;
Medical Genomics and Metabolic Genetics Branch National Human Genome Research Institute NIH;
HudsonAlpha Institute for Biotechnology;
HudsonAlpha Institute for Biotechnology;
National Cancer Institute National Institutes of Health;
Department of Bioethics and Humanities University of Washington;
Departments of Pediatrics and Genetics and Genomic Sciences Icahn School of Medicine at Mount Sinai;
Center for Health Research Kaiser Permanente Northwest;
National Institute on Minority Health and Health Disparities National Institutes of Health;
Division of Medical Genetics Department of Medicine University of Washington;
Department of Health Policy and Management Gillings School of Global Public Health University of;
Department of Anthropology History &
Social Medicine Helen Diller Family Comprehensive Cancer;
Department of Genetics and Genomics Icahn School of Medicine at Mount Sinai;
Program in Bioethics Institute for Health and Aging University of California-San Francisco;
Division of Preventive Medicine University of Alabama at Birmingham and Birmingham VA Medical;
Institute for Human Genetics University of California San Francisco;
Medical Genomics and Metabolic Genetics Branch National Human Genome Research Institute NIH;
Center for Medical Ethics and Health Policy Baylor College of Medicine;
Department of Obstetrics Gynecology and Reproductive Sciences University of California;
Division of Medical Genetics Department of Medicine University of Washington;
Texas Children’s Cancer Center and Department of Pediatrics Baylor College of Medicine;
Department of Genetics University of North Carolina at Chapel Hill;
Institute for Human Genetics University of California San Francisco;
Bethel Gospel Assembly;
Department of Biomedical Research John Theurer Cancer Center Hackensack University Medical Center;
Department of Pediatrics Baylor College of Medicine;
Department of Pediatrics Division of Genetics University of California San Francisco;
Department of Pharmacy University of Washington;
Children’s Hospital at Montefiore Albert Einstein College of Medicine;
Department of Pediatrics and Seattle Children’s Research Institute University of Washington;
Division of Genomic Medicine National Human Genome Research Institute NIH;
Department of Pediatrics Baylor College of Medicine;
Division of Medical Genetics Department of Medicine University of Washington;
机译:临床测序循证事项研究联盟:在多种和医学欠缺的人群中整合基因组测序
机译:基因组测序中的社会和行为研究:来自临床测序探索性研究联盟成果和措施工作组的方法。
机译:临床测序探索性研究联盟:加速基于证据的基因组医学实践
机译:一种综合框架,用于报告来自配对肿瘤/正常基因组和转录组序列测序数据的临床相关的生物标志物,以支持个性化医学中的临床试验
机译:使用大规模平行测序和微阵列的乳腺癌基因组学的分子表征和临床实施。
机译:临床测序证据产生研究联合会:整合基因组测序在不同人群和医疗不足人群中的应用
机译:基因组测序结果披露在不同的和医学方面的人口:CSER财团的主题,挑战和战略