Facilitating genome navigation:: survey sequencing and dense radiation-hybrid gene mapping

被引:53
作者
Hitte, C
Madeoy, J
Kirkness, EF
Priat, C
Lorentzen, TD
Senger, F
Thomas, D
Derrien, T
Ramirez, C
Scott, C
Evanno, G
Pullar, B
Cadieu, E
Oza, V
Lourgant, K
Jaffe, DB
Tacher, S
Dréano, S
Berkova, N
André, C
Deloukas, P
Fraser, C
Lindblad-Toh, K
Ostrander, EA
Galibert, F
机构
[1] NHGRI, NIH, Bethesda, MD 20892 USA
[2] Fac Med, CNRS, UMR 6061, F-35043 Rennes, France
[3] Fred Hutchinson Canc Res Ctr, Div Human Biol, Seattle, WA 98109 USA
[4] Fred Hutchinson Canc Res Ctr, Div Clin Res, Seattle, WA 98109 USA
[5] Inst Genome Res, Rockville, MD 20850 USA
[6] Wellcome Trust Sanger, Inst Hixton, Hixton, Cambs, England
[7] MIT, Broad Inst, Cambridge, MA 02141 USA
[8] Harvard Univ, Cambridge, MA 02141 USA
基金
英国惠康基金;
关键词
D O I
10.1038/nrg1658
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Accurate and comprehensive sequence coverage for large genomes has been restricted to only a few species of specific interest. Lower sequence coverage (survey sequencing) of related species can yield a wealth of information about gene content and putative regulatory elements. But survey sequences lack long-range continuity and provide only a fragmented view of a genome. Here we show the usefulness of combining survey sequencing with dense radiation-hybrid (RH) maps for extracting maximum comparative genome information from model organisms. Based on results from the canine system, we propose that from now on all low-pass sequencing projects should be accompanied by a dense, gene-based RH map-construction effort to extract maximum information from the genome with a marginal extra cost.
引用
收藏
页码:643 / 649
页数:7
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