Jim Ostell, Ph.D.
NIH Distinguished Investigator
Information Engineering Branch
Building 45, Room 5AN44A
45 Center Drive
Bethesda, MD 20894
As IEB Chief, Dr. Ostell has been responsible for designing, developing, building, and deploying almost all production resources at NCBI from its beginning including PubMed, GenBank, BLAST, Entrez, RefSeq, dbSNP, PubMed Central, dbGaP, and many others. IEB serves more than 2 million users a day at peak rates of more than 5,000 Web hits a second.
Dr. Ostell is the Chief of the Information Engineering Branch (IEB) of the National Center for Biotechnology Information (NCBI). Dr. Ostell earned a Ph.D. in molecular biology from Harvard University, developed commercial software for biotechnology, then helped create NCBI in 1988. In 2007 Dr. Ostell was inducted into the United States National Academies, Institute of Medicine, and made an NIH Distinguished Investigator in 2011.
Sayers EW, Barrett T, Benson DA, Bolton E, Bryant SH, Canese K, Chetvernin V, Church DM, Dicuccio M, Federhen S, Feolo M, Fingerman IM, Geer LY, Helmberg W, Kapustin Y, Krasnov S, Landsman D, Lipman DJ, Lu Z, Madden TL, Madej T, Maglott DR, Marchler-Bauer A, Miller V, Karsch-Mizrachi I, Ostell J, Panchenko A, Phan L, Pruitt KD, Schuler GD, Sequeira E, Sherry ST, Shumway M, Sirotkin K, Slotta D, Souvorov A, Starchenko G, Tatusova TA, Wagner L, Wang Y, Wilbur WJ, Yaschenko E, Ye J. Database resources of the National Center for Biotechnology Information. Nucleic Acids Res. 2012;40(Database issue):D13-25.
Craig DW, Goor RM, Wang Z, Paschall J, Ostell J, Feolo M, Sherry ST, Manolio TA. Assessing and managing risk when sharing aggregate genetic variant data. Nat Rev Genet. 2011;12(10):730-6.
Miller DT, Adam MP, Aradhya S, Biesecker LG, Brothman AR, Carter NP, Church DM, Crolla JA, Eichler EE, Epstein CJ, Faucett WA, Feuk L, Friedman JM, Hamosh A, Jackson L, Kaminsky EB, Kok K, Krantz ID, Kuhn RM, Lee C, Ostell JM, Rosenberg C, Scherer SW, Spinner NB, Stavropoulos DJ, Tepperberg JH, Thorland EC, Vermeesch JR, Waggoner DJ, Watson MS, Martin CL, Ledbetter DH. Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies. Am J Hum Genet. 2010;86(5):749-64.
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This page was last updated on October 26th, 2017