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BMJ (Clinical Research Ed.)|May 30, 2015
Diagnosis and treatment of cancer using genomicsJoseph G Vockley, John E NiederhuberPlos One|December 19, 2015
CloudForest: A Scalable and Efficient Random Forest Implementation for Biological DataRyan Bressler, Richard B Kreisberg, Brady Bernard, et al.Plos One|April 15, 2014
Germline variation in cancer-susceptibility genes in a healthy, ancestrally diverse cohort: implications for individual genome sequencingDale L Bodian, Justine N McCutcheon, Prachi Kothiyal, et al.American Journal of Medical Genetics. Part A|February 26, 2015
Expanding the phenotypic spectrum in EP300-related Rubinstein-Taybi syndromeBenjamin D Solomon, Dale L Bodian, Alina Khromykh, et al.Molecular Genetics & Genomic Medicine|January 24, 2015
Diagnosis of an imprinted-gene syndrome by a novel bioinformatics analysis of whole-genome sequences from a family trioDale L Bodian, Benjamin D Solomon, Alina Khromykh, et al.Molecular Syndromology|January 7, 2016
Diagnosis of D-Bifunctional Protein Deficiency through Whole-Genome Sequencing: Implications for Cost-Effective CareAlina Khromykh, Benjamin D Solomon, Dale L Bodian, et al.Nature Communications|January 20, 2016
New observations on maternal age effect on germline de novo mutationsWendy S W Wong, Benjamin D Solomon, Dale L Bodian, et al.Frontiers in Genetics|March 6, 2015
Identification of copy number variants in whole-genome data using Reference Coverage ProfilesGustavo Glusman, Alissa Severson, Varsha Dhankani, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 4, 2015
Utility of whole-genome sequencing for detection of newborn screening disorders in a population cohort of 1,696 neonatesDale L Bodian, Elisabeth Klein, Ramaswamy K Iyer, et al.Oncotarget|October 21, 2015
Systematic evaluation of underlying defects in DNA repair as an approach to case-only assessment of familial prostate cancerEmmanuelle Nicolas, Sanjeevani Arora, Yan Zhou, et al.Pageof 2