Mapping segmental and sequence variations among laboratory mice using BAC array CGH
Author(s) -
Antoine M. Snijders,
Norma J. Nowak,
Bing Huey,
Jane Fridlyand,
Sindy Law,
Jeffrey M. Conroy,
Taku A. Tokuyasu,
Kubilay Demir,
Readman Chiu,
JianHua Mao,
Ajay N. Jain,
Steven J.M. Jones,
Allan Balmain,
Daniel Pinkel,
Donna G. Albertson
Publication year - 2005
Publication title -
genome research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.556
H-Index - 297
eISSN - 1549-5469
pISSN - 1088-9051
DOI - 10.1101/gr.2902505
Subject(s) - biology , genetics , chromosome , genotyping , genome , microbiology and biotechnology , backcrossing , gene , genotype
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 (|log(2)ratio| >/= 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 (Delta log(2)ratio approximately 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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