A Whole-Genome Mouse BAC Microarray With 1-Mb Resolution for Analysis of DNA Copy Number Changes by Array Comparative Genomic Hybridization
Author(s) -
YeunJun Chung,
Jos Jonkers,
Hannah Kitson,
Heike Fiegler,
Sean Humphray,
Carol Scott,
Sarah Hunt,
Yuejin Yu,
Ichiko Nishijima,
Arno Velds,
Henne Holstege,
Nigel Carter,
Allan Bradley
Publication year - 2004
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.1878804
Subject(s) - biology , dna microarray , comparative genomic hybridization , genomic dna , bacterial artificial chromosome , genetics , genome , microbiology and biotechnology , genomic library , microarray , tiling array , dna , gene , gene expression , base sequence
Microarray-based comparative genomic hybridization (CGH) has become a powerful method for the genome-wide detection of chromosomal imbalances. Although BAC microarrays have been used for mouse CGH studies, the resolving power of these analyses was limited because high-density whole-genome mouse BAC microarrays were not available. We therefore developed a mouse BAC microarray containing 2803 unique BAC clones from mouse genomic libraries at 1-Mb intervals. For the general amplification of BAC clone DNA prior to spotting, we designed a set of three novel degenerate oligonucleotide-primed (DOP) PCR primers that preferentially amplify mouse genomic sequences while minimizing unwanted amplification of contaminating Escherichia coli DNA. The resulting 3K mouse BAC microarrays reproducibly identified DNA copy number alterations in cell lines and primary tumors, such as single-copy deletions, regional amplifications, and aneuploidy.
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