Generation of a high-density rat EST map

被引:28
作者
Scheetz, TE
Raymond, MR
Nishimura, DY
McClain, A
Roberts, C
Birkett, C
Gardiner, J
Zhang, J
Butters, N
Sun, C
Kwitek-Black, A
Jacob, H
Casavant, TL
Soares, MB
Sheffield, VC [1 ]
机构
[1] Univ Iowa, Howard Hughes Med Inst, Iowa City, IA 52242 USA
[2] Univ Iowa, Dept Pediat, Iowa City, IA 52242 USA
[3] Univ Iowa, Dept Physiol & Biophys, Iowa City, IA 52242 USA
[4] Univ Iowa, Dept Elect & Comp Engn, Iowa City, IA 52242 USA
[5] Univ Missouri, Dept Agron, Columbia, MO 65203 USA
[6] Med Coll Wisconsin, Dept Physiol, Lab Genet Res, Milwaukee, WI 53226 USA
关键词
D O I
10.1101/gr.GR-1516R
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have developed a high-density EST map of the rat, consisting of >11,000 ESTs. These ESTs were placed on a radiation hybrid framework map of genetic markers spanning all 20 rat autosomes, plus the X chromosome. The framework maps have a total size of similar to 12,400 cR, giving an average correspondence of 240 kb/cR. The frameworks are all LOD 3 chromosomal maps consisting of 775 radiation-hybrid-mapped genetic markers and ESTs. To date, we have generated radiation-hybrid-mapping data for >14,000 novel ESTs identified by our Rat Gene Discovery and Mapping Project (http://ratEST.uiowa.edu), from which we have placed >11,000 on our framework maps. To minimize mapping errors, ESTs were mapped in duplicate and consensus RH vectors produced for use in the placement procedure. This EST map was then used to construct high-density comparative maps between rat and human and rat and mouse. These maps will be a useful resource for positional cloning of genes for rat models of human diseases and in the creation and verification of a tiling set of map order for the upcoming rat-genome sequencing.
引用
收藏
页码:497 / 502
页数:6
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