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图谱错误减少:利用基于遗传和序列的物理图谱对紧密连锁的标记进行排序。

Map error reduction: using genetic and sequence-based physical maps to order closely linked markers.

作者信息

DeWan Andrew T, Parrado Antonio R, Matise Tara C, Leal Suzanne M

机构信息

The Laboratory of Statistical Genetics, The Rockefeller University, New York, NY, USA.

出版信息

Hum Hered. 2002;54(1):34-44. doi: 10.1159/000066697.

Abstract

The Marshfield comprehensive genetic maps are frequently used for linkage and association studies, however, for some regions of these maps the marker order has low level of likelihood ratio support. In order to investigate the level of statistical support and the accuracy of the genetic maps compared to sequence-based physical maps, two approximately 30 cM autosomal regions were selected. The first region was selected from chromosome 3 and consisted predominately of draft sequence. The second region was selected from chromosome 21 and consisted of finished sequence data. The physical order of these markers was based upon their position on Celera (CEL) and Human Genome Project-Santa Cruz (HGP-sc) sequence-based physical maps. The chromosome 3 and 21 regions contained 100 and 61 markers, respectively, on the Marshfield genetic map. The genetic and physical map order was consistent for 88.9 and 89.2% of the markers in the region on chromosome 3 and 21, respectively. Using a novel scoring criterion to assess inconsistent marker order between genetic and physical maps, it was determined that the physical order was likely the correct order for 3.3 and 7.1% of the markers in the chromosome 3 and 21 regions, respectively. To increase the accuracy of the order of markers selected for fine mapping a method is presented which combines information from genetic and sequence-based physical maps.

摘要

马什菲尔德综合遗传图谱经常用于连锁和关联研究,然而,在这些图谱的某些区域,标记顺序的似然比支持水平较低。为了研究与基于序列的物理图谱相比,遗传图谱的统计支持水平和准确性,选择了两个大约30厘摩的常染色体区域。第一个区域选自由草图序列为主构成的3号染色体。第二个区域选自由完成序列数据构成的21号染色体。这些标记的物理顺序基于它们在赛雷拉(CEL)和人类基因组计划-圣克鲁兹(HGP-sc)基于序列的物理图谱上的位置。在马什菲尔德遗传图谱上,3号和21号染色体区域分别包含100个和61个标记。在3号和21号染色体区域,分别有88.9%和89.2%的标记的遗传图谱和物理图谱顺序是一致的。使用一种新颖的评分标准来评估遗传图谱和物理图谱之间不一致的标记顺序,结果确定在3号和21号染色体区域,分别有3.3%和7.1%的标记的物理顺序可能是正确顺序。为了提高选择用于精细定位的标记顺序的准确性,提出了一种结合遗传图谱和基于序列的物理图谱信息的方法。

相似文献

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本文引用的文献

1
Systematic evaluation of map quality: human chromosome 22.图谱质量的系统评估:人类22号染色体
Am J Hum Genet. 2002 Jun;70(6):1398-410. doi: 10.1086/340605. Epub 2002 Apr 19.
10
The sequence of the human genome.人类基因组序列。
Science. 2001 Feb 16;291(5507):1304-51. doi: 10.1126/science.1058040.

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