Schalkwyk, Leonard C and Cusack, Brian and Dunkel, Ilona and Hopp, Martina and Kramer, Markus and Palczewski, Stefanie and Piefke, Jutta and Scheel, Sabine and Weiher, Michael and Wenske, Gunther and Lehrach, Hans and Himmelbauer, Heinz (2001) Advanced Integrated Mouse YAC Map Including BAC Framework. Genome Research, 11 (12). pp. 2142-2150. DOI https://doi.org/10.1101/gr.176201
Schalkwyk, Leonard C and Cusack, Brian and Dunkel, Ilona and Hopp, Martina and Kramer, Markus and Palczewski, Stefanie and Piefke, Jutta and Scheel, Sabine and Weiher, Michael and Wenske, Gunther and Lehrach, Hans and Himmelbauer, Heinz (2001) Advanced Integrated Mouse YAC Map Including BAC Framework. Genome Research, 11 (12). pp. 2142-2150. DOI https://doi.org/10.1101/gr.176201
Schalkwyk, Leonard C and Cusack, Brian and Dunkel, Ilona and Hopp, Martina and Kramer, Markus and Palczewski, Stefanie and Piefke, Jutta and Scheel, Sabine and Weiher, Michael and Wenske, Gunther and Lehrach, Hans and Himmelbauer, Heinz (2001) Advanced Integrated Mouse YAC Map Including BAC Framework. Genome Research, 11 (12). pp. 2142-2150. DOI https://doi.org/10.1101/gr.176201
Abstract
<jats:p>Functional characterization of the mouse genome requires the availability of a comprehensive physical map to obtain molecular access to chromosomal regions of interest. Positional cloning remains a crucial way of linking phenotype with particular genes. A key step and frequent stumbling block in positional cloning is making a contig of a genetically defined candidate region. The most efficient first step is isolating YAC (Yeast Artificial Chromosome) clones. A robust, detailed YAC contig map is thus an important tool. Employing Interspersed Repetitive Sequence (IRS)-PCR genomics, we have generated an advanced second-generation YAC contig map of the mouse genome that doubles both the depth of clones and the density of markers available. In addition to the primarily YAC-based map, we located 1942 BAC (Bacterial Artificial Chromosome) clones. This allows us to present for the first time a dense framework of BACs spanning the genome of the mouse, which, for instance, can serve as a nucleus for genomic sequencing. Four large-insert mouse YAC libraries from three different strains are included in our data, and our analysis incorporates the data of Hunter et al. and Nusbaum et al. There is a total of 20,205 markers on the final map, 12,033 from our own data, and a total of 56,093 YACs, of which 44,401 are positive for more than one marker.</jats:p><jats:p>[The sequence data described in this paper have been submitted to the GenBank data library under accession nos. <jats:ext-link xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="BH174059" ext-link-type="gen" xlink:type="simple">BH174059</jats:ext-link>–<jats:ext-link xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="BH175013" ext-link-type="gen" xlink:type="simple">BH175013</jats:ext-link>.]</jats:p>
Item Type: | Article |
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Uncontrolled Keywords: | Chromosomes, Artificial, Bacterial; Chromosomes, Artificial, Yeast; Animals; Mice; Physical Chromosome Mapping; Contig Mapping; Nucleic Acid Hybridization; Algorithms; Computer Simulation; Molecular Sequence Data; Databases, Genetic |
Subjects: | Q Science > QH Natural history > QH426 Genetics |
Divisions: | Faculty of Science and Health Faculty of Science and Health > Life Sciences, School of |
SWORD Depositor: | Unnamed user with email elements@essex.ac.uk |
Depositing User: | Unnamed user with email elements@essex.ac.uk |
Date Deposited: | 01 Aug 2017 14:55 |
Last Modified: | 30 Oct 2024 15:58 |
URI: | http://repository.essex.ac.uk/id/eprint/11102 |