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The direct screening of cosmid libraries with YAC clones.

作者信息

Baxendale S, Bates G P, MacDonald M E, Gusella J F, Lehrach H

机构信息

Genome Analysis Laboratory, Imperial Cancer Research Fund, London, UK.

出版信息

Nucleic Acids Res. 1991 Dec 11;19(23):6651. doi: 10.1093/nar/19.23.6651.

DOI:10.1093/nar/19.23.6651
PMID:1754409
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC329250/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f91/329250/4925bcf56121/nar00103-0283-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f91/329250/4925bcf56121/nar00103-0283-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f91/329250/4925bcf56121/nar00103-0283-a.jpg

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本文引用的文献

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"A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum.一种将DNA限制性内切酶片段放射性标记至高比活度的技术。附录
Anal Biochem. 1984 Feb;137(1):266-7. doi: 10.1016/0003-2697(84)90381-6.
2
Cloning of large segments of exogenous DNA into yeast by means of artificial chromosome vectors.通过人工染色体载体将大片段外源DNA克隆到酵母中。
Science. 1987 May 15;236(4803):806-12. doi: 10.1126/science.3033825.
3
Detection of deletions spanning the Duchenne muscular dystrophy locus using a tightly linked DNA segment.
一张整合了酵母人工染色体（YACs）、基因和序列标签位点（STS）标记的覆盖整个人类X染色体的辐射杂种图谱。
Mamm Genome. 1996 Oct;7(10):758-66. doi: 10.1007/s003359900227.
4
Exon-enriched probe derived from a human chromosome 21 YAC by exon-amplification.通过外显子扩增从人21号染色体酵母人工染色体（YAC）获得的富含外显子的探针。
Nucleic Acids Res. 1993 May 11;21(9):2271-2. doi: 10.1093/nar/21.9.2271.
5
Characterization of a cosmid library from flow-sorted chromosomes 11.来自流式分选的11号染色体的黏粒文库的特征分析。
Chromosome Res. 1994 May;2(3):201-7. doi: 10.1007/BF01553320.
6
Efficient identification and regional positioning of YAC and cosmid clones to human chromosome 21 by radiation fusion hybrids.通过辐射杂种细胞将YAC和黏粒克隆高效鉴定并定位到人类21号染色体上。
Mamm Genome. 1994 Jun;5(6):365-71. doi: 10.1007/BF00356556.
7
A method for screening arrayed cosmid libraries with mega insert yeast artificial chromosomes.一种利用大插入片段酵母人工染色体筛选阵列黏粒文库的方法。
Nucleic Acids Res. 1995 Mar 25;23(6):1085-6. doi: 10.1093/nar/23.6.1085.
利用紧密连锁的DNA片段检测跨越杜氏肌营养不良症基因座的缺失
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A DNA segment encoding two genes very tightly linked to Huntington's disease.一段编码与亨廷顿舞蹈症紧密连锁的两个基因的DNA片段。
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