Methods

Mapping segmental and sequence variations among laboratory mice using BAC array CGH

    • 1 Cancer Research Institute, University of California San Francisco, San Francisco, California 94143, USA
    • 2 Department of Laboratory Medicine, University of California San Francisco, San Francisco, California 94143, USA
    • 3 Roswell Park Cancer Institute, Buffalo, New York 14263, USA
    • 4 Genome Sequence Centre, British Columbia Cancer Research Centre, Vancouver, British Columbia, Canada V5Z-4E6
Published February 1, 2005. Vol 15 Issue 2, pp. 302-311. https://doi.org/10.1101/gr.2902505
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Abstract

We used arrays of 2069 BACs (1303 nonredundant autosomal clones) to map sequence variation among Mus spretus (SPRET/Ei and SPRET/Glasgow) and Mus musculus (C3H/HeJ, BALB/cJ, 129/J, DBA/2J, NIH, FVB/N, and C57BL/6) strains. We identified 80 clones representing 74 autosomal loci of copy number variation (|log2ratio| ≥ 0.4). These variant loci distinguish laboratory strains. By FISH mapping, we determined that 63 BACs mapped to a single site on C57BL/6J chromosomes, while 17 clones mapped to multiple chromosomes (n = 16) or multiple sites on one chromosome (n = 1). We also show that small ratio changes (Δ log2ratio ∼ 0.1) distinguish homozygous and heterozygous regions of the genome in interspecific backcross mice, providing an efficient method for genotyping progeny of backcrosses.

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