The proposal requests support for fifteen predoctoral and six postdoctoral trainees in a multidisciplinary program in Genomics at the University of California, Berkeley (UCB). We define genomics broadly as the acquisition and analysis of high-throughput genome-scale data in biology, and the exploitation of the resulting data to solve biomedical problems. The (20) twenty participating faculty at UCB are drawn from nine Departments (Molecular and Cell Biology, Physics, Chemistry, Mechanical Engineering, Integrative Biology, Public Health, Nutrition, and Computer Science). Research mentors are also available at the nearby Lawrence Berkeley National Laboratory (LBNL), which is home to national centers for microscopy, imaging, supercomputing, and synchrotron radiation. Students can be admitted to the program throughout the Ph.D. programs of any of the participating UCB departments. In addition to rigorous training in their home departments, a wide range of didactic courses are available for training in complementary disciplines to provide trainees with exposure to technology development for genomics, important biological and biomedical problems that can be attacked by new technologies, and computational approaches to analysis and mining of genomic data. Trainees typically spend three consecutive ten-week periods rotating though different laboratories of their choice selected from a diverse array of research environments at UC Berkeley or at LBNL. The specific multidisciplinary course of study for each trainee will be chosen in consultation with a pair of faculty mentors, one from biology and one from the physical sciences or engineering. Students typically take their oral qualifying exams by the end of the second year, and begin to engage in research projects. In years 3-5 trainees carry out their dissertation research, continue to teach and take advanced courses, and participate in seminars, group meetings, and retreats to expand their skills. Applicants to the participating departments typically have outstanding undergraduate records in the biological, chemical, or physical sciences, or engineering. Admission is based on evaluation of previous scholastic achievement, prior research experience and performance scores on standardized exams, statement of purpose and letters of recommendation.

Agency
National Institute of Health (NIH)
Institute
National Human Genome Research Institute (NHGRI)
Type
Institutional National Research Service Award (T32)
Project #
5T32HG000047-03
Application #
6536456
Study Section
Ethical, Legal, Social Implications Review Committee (GNOM)
Program Officer
Graham, Bettie
Project Start
2000-09-01
Project End
2005-06-30
Budget Start
2002-07-09
Budget End
2003-06-30
Support Year
3
Fiscal Year
2002
Total Cost
$687,964
Indirect Cost
Name
University of California Berkeley
Department
Biochemistry
Type
Schools of Arts and Sciences
DUNS #
094878337
City
Berkeley
State
CA
Country
United States
Zip Code
94704
Street, Kelly; Risso, Davide; Fletcher, Russell B et al. (2018) Slingshot: cell lineage and pseudotime inference for single-cell transcriptomics. BMC Genomics 19:477
Van Dalfsen, Kelsey Marie; Hodapp, Stefanie; Keskin, Abdurrahman et al. (2018) Global Proteome Remodeling during ER Stress Involves Hac1-Driven Expression of Long Undecoded Transcript Isoforms. Dev Cell 46:219-235.e8
Erickson, Priscilla A; Baek, Jiyeon; Hart, James C et al. (2018) Genetic Dissection of a Supergene Implicates Tfap2a in Craniofacial Evolution of Threespine Sticklebacks. Genetics 209:591-605
Mok, Amanda; Rhead, Brooke; Holingue, Calliope et al. (2018) Hypomethylation of CYP2E1 and DUSP22 Promoters Associated With Disease Activity and Erosive Disease Among Rheumatoid Arthritis Patients. Arthritis Rheumatol 70:528-536
Lyons, David B; Zilberman, Daniel (2017) DDM1 and Lsh remodelers allow methylation of DNA wrapped in nucleosomes. Elife 6:
Gianfrancesco, Milena A; Stridh, Pernilla; Shao, Xiaorong et al. (2017) Genetic risk factors for pediatric-onset multiple sclerosis. Mult Scler :1352458517733551
Rhead, Brooke; Holingue, Calliope; Cole, Michael et al. (2017) Rheumatoid Arthritis Naive T Cells Share Hypermethylation Sites With Synoviocytes. Arthritis Rheumatol 69:550-559
Hart, James C; Miller, Craig T (2017) Sequence-Based Mapping and Genome Editing Reveal Mutations in Stickleback Hps5 Cause Oculocutaneous Albinism and the casper Phenotype. G3 (Bethesda) 7:3123-3131
Stadler, Michael R; Haines, Jenna E; Eisen, Michael B (2017) Convergence of topological domain boundaries, insulators, and polytene interbands revealed by high-resolution mapping of chromatin contacts in the early Drosophila melanogaster embryo. Elife 6:
Gianfrancesco, Milena A; Stridh, Pernilla; Rhead, Brooke et al. (2017) Evidence for a causal relationship between low vitamin D, high BMI, and pediatric-onset MS. Neurology 88:1623-1629

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