ComboScreen facilitates the multiplex hybridization-based screening of high-density clone arrays

被引:9
作者
Jamison, DC [1 ]
Thomas, JW [1 ]
Green, ED [1 ]
机构
[1] Natl Human Genome Res Inst, Genome Technol Branch, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1093/bioinformatics/16.8.678
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: The construction of physical maps based on bacterial clones [e.g. bacterial artificial chromosomes (BACs)] is valuable for a number of molecular genetics applications, including the high-resolution mapping of genomic regions of interest and the identification of clones suitable for systematic sequencing A common approach for large-scale screening of bacterial clone libraries involves the hybridization of high-density arrays of immobilized, lysed colonies with collections of DNA probes. The use of a multiplex hybridization screening strategy, whereby pooled probes are analysed en masse, simplifies the effort by reducing the total number of parallel experiments required. However this approach generates large amounts of hybridization-based data that must be carefully analysed, assimilated, and disambiguated in a careful but efficient manner Results: To facilitate the screening of high-density clone arrays by a multiplex hybridization approach, Me have written a program called ComboScreen. This program provides an organizational framework and analytical tools required for the high-throughput hybridization screening of clone arrays with pools of probes. We have used this program extensively for constructing mouse sequence ready BAC contig maps.
引用
收藏
页码:678 / 684
页数:7
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