The first linkage disequilibrium (LD) maps: Delineation of hot and cold blocks by diplotype analysis

被引:134
作者
Maniatis, N
Collins, A
Xu, CF
McCarthy, LC
Hewett, DR
Tapper, W
Ennis, S
Ke, X
Morton, NE [1 ]
机构
[1] Univ Southampton, Southampton Gen Hosp, Div Human Genet, Southampton SO16 6YD, Hants, England
[2] Glaxo Wellcome Res & Dev Ltd, UK Discovery Genet, Stevenage SG1 2NY, Herts, England
关键词
D O I
10.1073/pnas.042680999
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Linkage disequilibrium (LD) provides information about positional cloning, linkage, and evolution that cannot be inferred from other evidence, even when a correct sequence and a linkage map based on more than a handful of families become available. We present theory to construct an LID map for which distances are additive and population-specific maps are expected to be approximately proportional. For this purpose, there is only a modest difference in relative efficiency of haplotypes and diplotypes: resolving the latter into 2-locus haplotypes has significant cost or error and increases information by about 50%. LID maps for a cold spot in 19p13.3 and a more typical region in 3q21 are optimized by interval estimates. For a random sample and trustworthy map the value of LID at large distance can be predicted reliably from information over a small distance and does not depend on the evolutionary variance unless the sample size approaches the population size. Values of the association probability that can be distinguished from the value at large distance are determined not by population size but by time since a critical bottleneck. in these examples, omission of markers with significant Hardy-Weinberg disequilibrium does not improve the map, and widely discrepant draft sequences have similar estimates of the genetic parameters. The LID cold spot in 19p13.3 gives an unusually high estimate of time, supporting an argument that this relationship is general. As predicted for a region with ancient haplotypes or uniformly high recombination, there is no clear evidence of LID clustering. On the contrary, the 3q21 region is resolved into alternating blocks of stable and decreasing LID, as expected from crossover clustering. Construction of a genomewide LID map requires data not yet available, which may be complemented but not replaced by a catalog of haplotypes.
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页码:2228 / 2233
页数:6
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