1 / 10

Functional Annotation of Animal Genomes (FAANG)

Functional Annotation of Animal Genomes (FAANG). Ravi N. Ravindranath, Ph.D . Fertility and Infertility Branch Eunice Kennedy Shriver National Institute of Child Health and Human Development National Institutes of Health. Is FAANG important for NIH?.

kioshi
Download Presentation

Functional Annotation of Animal Genomes (FAANG)

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript

  1. Functional Annotation of Animal Genomes (FAANG) Ravi N. Ravindranath, Ph.D. Fertility and Infertility Branch Eunice Kennedy Shriver National Institute of Child Health and Human Development National Institutes of Health

  2. Is FAANG important for NIH? Associating sequence variation with quantitative phenotypes has been done in domestic animals for a few decades because of the importance of animals : • As food sources • Models for human health/disease • Ecology

  3. Exploring Horizons for Domestic Animal Genomics • Meeting was held at NAS in 2002 • NIH perspective at the Meeting: • Sequencing is essential for basic scientific understanding • Sequencing is essential for human health and medical research • Reasons: • Understanding of human biology or physiology is based on domestic animal biology: Chicken embryology • Several methods developed in animals: IVF/Cloning • Disease models: Influenza

  4. NIH Participation • Cattle Genome Project (Baylor College of Medicine), NHGRI • Horse Genome Project (MIT), NHGRI • Chicken Genome Project (Washington University), NHGRI • Although there is no direct involvement with Swine Genome Project, NIH has always been interested in Swine as a model for growth, development, and disease since the pattern of growth and development of pigs is more similar to human. Several individual projects have been funded by NIH over the years.

  5. Models for Basic and Applied studies • Physiology • Nutrition • Pregnancy and fetal growth • Immunology • Organ transplantation • Infectious diseases • *Much less used as genetic models

  6. From Genomes…… What is critically important: • Functional Annotation of these genomes is necessary for knowing what is conserved and what is not • Genome to phenome correlation • Easy access of data to the investigators

  7. NIH-USDA Partnership: Research in Biomedicine and Agriculture Using Agriculturally Important Domestic Species(PAR13-204)

  8. Priority Areas • Assisted Reproduction Technologies/Stem Cell Biology: Oocyte Biology; Embyro Competence and Viability; SCNT; iPSC; Transgenesis; Male Germline Development • Metabolism: Obesity • Developmental Origin of Adult Diseases: In-Utero Developmental Programming • Infectious Diseases and Applied Immunology

  9. Projects of Relevance to FAANG Objectives • 1. Pablo Ross, University of California, Davis; Epigenetic Control of Preimplantation Development (R01HD070044) • 2. R. Michael Roberts, University of Missouri-Columbia; Induced Pluripotent Stem Cells from Swine: Application to Genetic Modification (R01HD069979) • 3. Thomas Spencer, Washington State University, Pullman; Systems Biology Approach to understand Endometrial Receptivity and Pregnancy (R01HD072898) • 4. Randall Prather, University of Missouri, Columbia, MO. Modification of SCNT donor cell metabolism to mimic blastomere metabolism (R01HD080636) • 5. Bhanu Prakash Telugu, University of Maryland, College Park, MD. Generation of zoonotic influenza resistant recominant pigs via site-directed technology (USDA)

  10. Questions?ravindrn@mail.nih.gov301-435-6889

More Related