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Cloning and genomic organization of the mouse gene slc23a1 encoding a vitamin C transporter.
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Analysis of the genome sequence of the flowering plant Arabidopsis thaliana.开花植物拟南芥的基因组序列分析。
Nature. 2000 Dec 14;408(6814):796-815. doi: 10.1038/35048692.
3
A 6-Mb high-resolution physical and transcription map encompassing the hereditary prostate cancer 1 (HPC1) region.一个覆盖遗传性前列腺癌1(HPC1)区域的6兆碱基对高分辨率物理图谱和转录图谱。
Genomics. 2000 Feb 15;64(1):1-14. doi: 10.1006/geno.1999.6051.
4
Complementation of plant mutants with large genomic DNA fragments by a transformation-competent artificial chromosome vector accelerates positional cloning.通过具备转化能力的人工染色体载体用大基因组DNA片段对植物突变体进行互补作用可加速图位克隆。
Proc Natl Acad Sci U S A. 1999 May 25;96(11):6535-40. doi: 10.1073/pnas.96.11.6535.
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High throughput fingerprint analysis of large-insert clones.大插入片段克隆的高通量指纹分析
Genome Res. 1997 Nov;7(11):1072-84. doi: 10.1101/gr.7.11.1072.
6
Functional identification of the mouse circadian Clock gene by transgenic BAC rescue.通过转基因细菌人工染色体(BAC)拯救对小鼠生物钟基因进行功能鉴定。
Cell. 1997 May 16;89(4):655-67. doi: 10.1016/s0092-8674(00)80246-9.
7
Construction and characterization of a bacterial artificial chromosome library of Sorghum bicolor.高粱(Sorghum bicolor)细菌人工染色体文库的构建与鉴定
Nucleic Acids Res. 1994 Nov 25;22(23):4922-31. doi: 10.1093/nar/22.23.4922.
8
The genome of Arabidopsis thaliana.拟南芥的基因组。
Proc Natl Acad Sci U S A. 1995 Nov 21;92(24):10831-5. doi: 10.1073/pnas.92.24.10831.
9
Cloning and stable maintenance of 300-kilobase-pair fragments of human DNA in Escherichia coli using an F-factor-based vector.利用基于F因子的载体在大肠杆菌中克隆和稳定保存300千碱基对的人类DNA片段。
Proc Natl Acad Sci U S A. 1992 Sep 15;89(18):8794-7. doi: 10.1073/pnas.89.18.8794.

BACFinder:基于限制性指纹图谱的大片段基因组克隆的基因组定位

BACFinder: genomic localisation of large insert genomic clones based on restriction fingerprinting.

作者信息

Crowe Mark L, Rana Debashis, Fraser Fiona, Bancroft Ian, Trick Martin

机构信息

John Innes Centre, Norwich Research Park, Colney, Norwich NR4 7UH, UK.

出版信息

Nucleic Acids Res. 2002 Nov 1;30(21):e118. doi: 10.1093/nar/gnf117.

DOI:10.1093/nar/gnf117
PMID:12409477
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC135841/
Abstract

We have developed software that allows the prediction of the genomic location of a bacterial artificial chromosome (BAC) clone, or other large genomic clone, based on a simple restriction digest of the BAC. The mapping is performed by comparing the experimentally derived restriction digest of the BAC DNA with a virtual restriction digest of the whole genome sequence. Our trials indicate that this program identified the genomic regions represented by BAC clones with a degree of accuracy comparable to that of end-sequencing, but at considerably less cost. Although the program has been developed principally for use with Arabidopsis BACs, it should align large insert genomic clones to any fully sequenced genome.

摘要

我们开发了一款软件,该软件能够基于细菌人工染色体(BAC)克隆或其他大型基因组克隆的简单限制性酶切,预测其基因组位置。通过将实验获得的BAC DNA限制性酶切结果与全基因组序列的虚拟限制性酶切结果进行比较来进行图谱绘制。我们的试验表明,该程序识别BAC克隆所代表的基因组区域的准确度与末端测序相当,但成本要低得多。尽管该程序主要是为拟南芥BAC而开发的,但它应该能够将大型插入基因组克隆与任何已完成全测序的基因组进行比对。