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A 12-Mb Complete Coverage BAC Contig Map in Human Chromosome 16p13.1–p11.2

机译:人类染色体16p13.1–p11.2中的12 Mb完全覆盖BAC重叠群图

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摘要

We have constructed a complete coverage BAC contig map that spans a 12-Mb genomic segment in the human chromosome 16p13.1–p11.2 region. The map consists of 68 previously mapped STSs and 289 BAC clones, 51 of which—corresponding to a total of 7.721 Mb of genomic DNA—have been sequenced, and provides a high resolution physical map of the region. Contigs were initially built based mainly on the analysis of STS contents and restriction fingerprint patterns of the clones. To close the gaps, probes derived from BAC clone ends were used to screen deeper BAC libraries. Clone end sequence data obtained from chromosome 16-specific BACs, as well as from public databases, were used for the identification of BACs that overlap with fully sequenced BACs by means of sequence match. This approach allowed precise alignment of clone overlaps in addition to restriction fingerprint comparison. A freehand contig drawing software tool was developed and used to manage the map data graphically and generate a real scale physical map. The map we present here is ∼3.5 × deep and provides a minimal tiling path that covers the region in an array of contigous, overlapping BACs.
机译:我们已经构建了覆盖人类染色体16p13.1–p11.2区域中12 Mb基因组片段的完整覆盖BAC重叠图。该图由68个先前定位的STS和289个BAC克隆组成,其中51个(对应于总共7.721 Mb的基因组DNA)已测序,并提供了该区域的高分辨率物理图。重叠群最初主要基于对STS含量和克隆的限制性指纹图谱的分析而构建。为了缩小差距,使用源自BAC克隆末端的探针筛选更深的BAC库。从16号染色体特异性BAC以及从公共数据库获得的克隆末端序列数据用于鉴定与序列完全匹配的BAC重叠的BAC。除了限制性指纹比较之外,该方法还允许克隆重叠的精确比对。开发了徒手的contig绘图软件工具,并将其用于以图形方式管理地图数据并生成真实比例的物理地图。我们在此处显示的地图深度约为3.5倍,并提供了一条最小的切片路径,该路径覆盖了一系列连续且重叠的BAC。

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