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Computational BAC clone contig assembly for comprehensive genome analysis
Author(s) -
Lapuk Anna,
Volik Stanislav,
Vincent Robert,
Chin Koei,
Kuo WenLin,
de Jong Pieter,
Collins Colin,
Gray Joe W.
Publication year - 2004
Publication title -
genes, chromosomes and cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.754
H-Index - 119
eISSN - 1098-2264
pISSN - 1045-2257
DOI - 10.1002/gcc.20016
Subject(s) - contig , bacterial artificial chromosome , genome , comparative genomic hybridization , biology , computational biology , chromosome , genetics , human genome , clone (java method) , dna , gene
Comparative genomic hybridization (CGH) has proved to be a powerful tool for the detection of genome copy number changes in human cancers and in other diseases caused by segmental aneusomies. Array versions of CGH allow the definition of these aberrations, with resolution determined by the size and distribution of the array elements. Resolution approaching 100 kb can be achieved by use of arrays comprising bacterial artificial chromosomes (BACs) distributed contiguously across regions of interest. We describe here a computer program that automatically assembles contigs of minimally overlapping BAC clones, using information about BAC end‐sequences and the normal genome DNA sequence. We demonstrate the characteristics of contigs assembled and annotated by use of this approach for regions of recurrent abnormality in human ovarian and breast cancers at chromosome bands 3q25–q27 and 8q24 and chromosome arm 20q. We also show illustrative analyses of regions of amplification in these regions in breast and ovarian tumor cell lines by use of array CGH with arrays comprising contiguous BACs. © 2004 Wiley‐Liss, Inc.