Integrated and Sequence-Ordered BAC- and YAC-Based Physical Maps for the Rat Genome

Martin Krzywinski(BC Cancer Agency), John Wallis(Washington University in St. Louis), Claudia Gösele(Max Planck Society), Ian Bosdet(BC Cancer Agency), Readman Chiu(BC Cancer Agency), Tina Graves(Washington University in St. Louis), Oliver Hummel(Max Delbrück Center), Dan Layman(Washington University in St. Louis), Carrie Mathewson(BC Cancer Agency), Natasja Wye(BC Cancer Agency), Baoli Zhu, Derek Albracht(Washington University in St. Louis), Jennifer Asano(BC Cancer Agency), Sarah Barber(BC Cancer Agency), Mabel Brown-John(BC Cancer Agency), Susanna Chan(BC Cancer Agency), Steve Chand(BC Cancer Agency), Alison Cloutier(BC Cancer Agency), Jonathon Davito(Washington University in St. Louis), Christopher D. Fjell(BC Cancer Agency), Tony Gaige(Washington University in St. Louis), Detlev Ganten(Max Delbrück Center), Noreen Girn(BC Cancer Agency), K Guggenheimer(University of British Columbia), Heinz Himmelbauer(Max Planck Society), Thomas Kreitler(Max Planck Society), Stephen Leach(BC Cancer Agency), Darlene Lee(BC Cancer Agency), Hans Lehrach(Max Planck Society), Michael Mayo(BC Cancer Agency), Kelly Mead(Washington University in St. Louis), Teika Olson(BC Cancer Agency), Pawan Pandoh(BC Cancer Agency), Anna-Liisa Prabhu(BC Cancer Agency), Heesun Shin(BC Cancer Agency), Simone Tänzer(National Institutes of Health), Jason D. Thompson(University of British Columbia), Miranda Tsai(BC Cancer Agency), Jason Walker(Washington University in St. Louis), George Yang(BC Cancer Agency), Mandeep Sekhon(Washington University in St. Louis), LaDeana Hillier(Washington University in St. Louis), Heike Zimdahl(Max Planck Society), Andre Marziali(University of British Columbia), Kazutoyo Osoegawa, Shaying Zhao(J. Craig Venter Institute), Asim Siddiqui(BC Cancer Agency), Pieter J. de Jong, Wes Warren(Washington University in St. Louis), Elaine R. Mardis(Washington University in St. Louis), John D. McPherson(Washington University in St. Louis), Richard Wilson(Washington University in St. Louis), Norbert Hübner(Max Delbrück Center), Steven J.M. Jones(BC Cancer Agency), Marco A. Marra(BC Cancer Agency), Jacqueline E. Schein(BC Cancer Agency)
Genome Research
April 1, 2004
Cited by 48Open Access
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Abstract

As part of the effort to sequence the genome of Rattus norvegicus, we constructed a physical map comprised of fingerprinted bacterial artificial chromosome (BAC) clones from the CHORI-230 BAC library. These BAC clones provide approximately 13-fold redundant coverage of the genome and have been assembled into 376 fingerprint contigs. A yeast artificial chromosome (YAC) map was also constructed and aligned with the BAC map via fingerprinted BAC and P1 artificial chromosome clones (PACs) sharing interspersed repetitive sequence markers with the YAC-based physical map. We have annotated 95% of the fingerprint map clones in contigs with coordinates on the version 3.1 rat genome sequence assembly, using BAC-end sequences and in silico mapping methods. These coordinates have allowed anchoring 358 of the 376 fingerprint map contigs onto the sequence assembly. Of these, 324 contigs are anchored to rat genome sequences localized to chromosomes, and 34 contigs are anchored to unlocalized portions of the rat sequence assembly. The remaining 18 contigs, containing 54 clones, still require placement. The fingerprint map is a high-resolution integrative data resource that provides genome-ordered associations among BAC, YAC, and PAC clones and the assembled sequence of the rat genome.


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