Skip to Content


A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 
An integrative variant analysis suite for whole exome next-generation sequencing data., Challis, Danny, Yu Jin, Evani Uday S., Jackson Andrew R., Paithankar Sameer, Coarfa Cristian, Milosavljevic Aleksandar, Gibbs Richard A., and Yu Fuli , BMC bioinformatics, 2012, Volume 13, p.8, (2012) Abstract
Internet Contig Explorer (iCE)--a tool for visualizing clone fingerprint maps., Fjell, Christopher D., Bosdet Ian, Schein Jacqueline E., Jones Steven J. M., and Marra Marco A. , Genome research, 2003 Jun, Volume 13, Issue 6A, p.1244-9, (2003) Abstract
PhenoDB: a new web-based tool for the collection, storage, and analysis of phenotypic features., Hamosh, Ada, Sobreira Nara, Hoover-Fong Julie, Sutton Reid V., Boehm Corinne, Schiettecatte François, and Valle David , Human mutation, 2013 Apr, Volume 34, Issue 4, p.566-71, (2013) Abstract
BEAUTY-X: enhanced BLAST searches for DNA queries., Worley, K. C., Culpepper P., Wiese B. A., and Smith R. F. , Bioinformatics (Oxford, England), 1998, Volume 14, Issue 10, p.890-1, (1998) Abstract
Large-scale concatenation cDNA sequencing., Yu, W., Andersson B., Worley K. C., Muzny D. M., Ding Y., Liu W., Ricafrente J. Y., Wentland M. A., Lennon G., and Gibbs R. A. , Genome research, 1997 Apr, Volume 7, Issue 4, p.353-8, (1997) Abstract
European admixture on the Micronesian island of Kosrae: lessons from complete genetic information., Bonnen, Penelope E., Lowe Jennifer K., Altshuler David M., Breslow Jan L., Stoffel Markus, Friedman Jeffrey M., and Pe'er Itsik , European journal of human genetics : EJHG, 2010 Mar, Volume 18, Issue 3, p.309-16, (2010) Abstract
Fine mapping and identification of candidate pulmonary adenoma susceptibility 1 genes using advanced intercross lines., Wang, Min, Lemon William J., Liu Gongjie, Wang Yian, Iraqi Fuad A., Malkinson Alvin M., and You Ming , Cancer research, 2003 Jun 15, Volume 63, Issue 12, p.3317-24, (2003) Abstract
PipMaker--a web server for aligning two genomic DNA sequences., Schwartz, S., Zhang Z., Frazer K. A., Smit A., Riemer C., Bouck J., Gibbs R., Hardison R., and Miller W. , Genome research, 2000 Apr, Volume 10, Issue 4, p.577-86, (2000) Abstract
A SNP discovery method to assess variant allele probability from next-generation resequencing data., Shen, Yufeng, Wan Zhengzheng, Coarfa Cristian, Drabek Rafal, Chen Lei, Ostrowski Elizabeth A., Liu Yue, Weinstock George M., Wheeler David A., Gibbs Richard A., et al. , Genome research, 2010 Feb, Volume 20, Issue 2, p.273-80, (2010) Abstract
dbNSFP: a lightweight database of human nonsynonymous SNPs and their functional predictions., Liu, Xiaoming, Jian Xueqiu, and Boerwinkle Eric , Human mutation, 2011 Aug, Volume 32, Issue 8, p.894-9, (2011) Abstract
The complete genome of an individual by massively parallel DNA sequencing., Wheeler, David A., Srinivasan Maithreyan, Egholm Michael, Shen Yufeng, Chen Lei, McGuire Amy, He Wen, Chen Yi-Ju, Makhijani Vinod, Roth Thomas G., et al. , Nature, 2008 Apr 17, Volume 452, Issue 7189, p.872-6, (2008) Abstract
The Atlas genome assembly system., Havlak, Paul, Chen Rui, Durbin James K., Egan Amy, Ren Yanru, Song Xing-Zhi, Weinstock George M., and Gibbs Richard A. , Genome research, 2004 Apr, Volume 14, Issue 4, p.721-32, (2004) Abstract
Identification of new members of a carbohydrate kinase-encoding gene family., Worley, K. C., King K. Y., Chua S., McCabe E. R., and Smith R. F. , Journal of computational biology : a journal of computational molecular cell biology, 1995 Fall, Volume 2, Issue 3, p.451-8, (1995) Abstract
nWayComp: a genome-wide sequence comparison tool for multiple strains/species of phylogenetically related microorganisms., Yao, Jiqiang, Lin Hong, Doddapaneni Harshavardhan, and Civerolo Edwin L. , In silico biology, 2007, Volume 7, Issue 2, p.195-200, (2007) Abstract
PBHoney: identifying genomic variants via long-read discordance and interrupted mapping., English, Adam C., Salerno William J., and Reid Jeffrey G. , BMC bioinformatics, 2014, Volume 15, p.180, (2014) Abstract
Identification of rat genes by TWINSCAN gene prediction, RT-PCR, and direct sequencing., Wu, Jiaqian, Shteynberg David, Arumugam Manimozhiyan, Gibbs Richard A., and Brent Michael R. , Genome research, 2004 Apr, Volume 14, Issue 4, p.665-71, (2004) Abstract
Software for automated analysis of DNA fingerprinting gels., Fuhrmann, Daniel R., Krzywinski Martin I., Chiu Readman, Saeedi Parvaneh, Schein Jacqueline E., Bosdet Ian E., Chinwalla Asif, Hillier Ladeana W., Waterston Robert H., McPherson John D., et al. , Genome research, 2003 May, Volume 13, Issue 5, p.940-53, (2003) Abstract
Loader Lite: a new software tool for the ABI PRISM 3700 DNA sequencer., Scott, G. B. I., Steffen D. L., Edgar D., Warren J. T., Kovár C. L., Scherer S. E., Havlak P. H., and Gibbs R. A. , BioTechniques, 2002 Jun, Volume 32, Issue 6, p.1366, 1368, 1370-1, (2002) Abstract
Pash 2.0: scaleable sequence anchoring for next-generation sequencing technologies., Coarfa, Cristian, and Milosavljevic Aleksandar , Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing, 2008, p.102-13, (2008) Abstract
PrimerSNP: a web tool for whole-genome selection of allele-specific and common primers of phylogenetically-related bacterial genomic sequences., Yao, Jiqiang, Lin Hong, Van Deynze Allen, Doddapaneni Harshavardhan, Francis Martha, Lemos Eliana Gertrudes Macedo, and Civerolo Edwin L. , BMC microbiology, 2008, Volume 8, p.185, (2008) Abstract
Working on the assembly line., Gibbs, R. A., and Cockerill M. , Trends in biochemical sciences, 1995 Apr, Volume 20, Issue 4, p.162-3, (1995)
Minimum information about a marker gene sequence (MIMARKS) and minimum information about any (x) sequence (MIxS) specifications., Yilmaz, Pelin, Kottmann Renzo, Field Dawn, Knight Rob, Cole James R., Amaral-Zettler Linda, Gilbert Jack A., Karsch-Mizrachi Ilene, Johnston Anjanette, Cochrane Guy, et al. , Nature biotechnology, 2011 May, Volume 29, Issue 5, p.415-20, (2011) Abstract
BEAUTY: an enhanced BLAST-based search tool that integrates multiple biological information resources into sequence similarity search results., Worley, K. C., Wiese B. A., and Smith R. F. , Genome research, 1995 Sep, Volume 5, Issue 2, p.173-84, (1995) Abstract
The Healthcare Administrator's Associate: an experiment in distributed healthcare information systems., Fowler, J., and Martin G. , Proceedings : a conference of the American Medical Informatics Association / ... AMIA Annual Fall Symposium. AMIA Fall Symposium, 1997, p.548-52, (1997) Abstract
Identification of mutations leading to the Lesch-Nyhan syndrome by automated direct DNA sequencing of in vitro amplified cDNA., Gibbs, R. A., Nguyen P. N., McBride L. J., Koepf S. M., and Caskey C. T. , Proceedings of the National Academy of Sciences of the United States of America, 1989 Mar, Volume 86, Issue 6, p.1919-23, (1989) Abstract

about seo