Virtual genome scan: A tool for restriction landmark-based scanning of the human genome

被引:31
作者
Rouillard, JM
Erson, AE
Kuick, R
Asakawa, J
Wimmer, K
Muleris, M
Petty, EM
Hanash, S [1 ]
机构
[1] Univ Michigan, Dept Pediat, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Communicable Dis, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Dept Human Genet, Ann Arbor, MI 48109 USA
[4] Univ Michigan, Dept Internal Med, Ann Arbor, MI 48109 USA
[5] Radiat Effects Res Fdn, Dept Genet, Hiroshima, Japan
[6] Univ Vienna, Inst Med Biol, A-1090 Vienna, Austria
[7] Inst Curie, UMR 147 CNRS, Lab Cytogenet Mol & Oncol, Paris, France
关键词
D O I
10.1101/gr.181601
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
There is substantial interest in implementing technologies that allow comparisons of whole genomes of individuals and of tissues and cell populations. Restriction landmark genome scanning (RLGS) is a highly resolving gel-based technique in which several thousand fragments in genomic digests are Visualized simultaneously and quantitatively analyzed. The widespread use of RLGS has been hampered by difficulty in deriving sequence information for displayed fragments and a lack of whole-genome sequence-based framework for interpreting RLGS patterns. We have developed informatics tools for comparisons of sample derived RLGS patterns with patterns predicted from the human genome sequence and displayed as Virtual Genome Scans (VGS). The tools developed allow sequence prediction of fragments in RLGS patterns obtained with different restriction enzyme combinations. The utility of VGS is demonstrated by the identification of restriction fragment length polymorphisms, and of amplifications, deletions, and methylation changes in tumor-derived CpG islands and the characterization of an amplified region in a breast tumor that spanned < 230 kb on 17q23.
引用
收藏
页码:1453 / 1459
页数:7
相关论文
共 35 条
[1]   Neuroblastoma cells can actively eliminate supernumerary MYCN gene copies by micronucleus formation -: sign of tumour cell revertance? [J].
Ambros, IM ;
Rumpler, S ;
Luegmayr, A ;
Hattinger, CM ;
Strehl, S ;
Kovar, H ;
Gadner, H ;
Ambros, PF .
EUROPEAN JOURNAL OF CANCER, 1997, 33 (12) :2043-2049
[2]   GENETIC-VARIATION DETECTED BY QUANTITATIVE-ANALYSIS OF END-LABELED GENOMIC DNA FRAGMENTS [J].
ASAKAWA, J ;
KUICK, R ;
NEEL, JV ;
KODAIRA, M ;
SATOH, C ;
HANASH, SM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (19) :9052-9056
[3]  
Barlund M, 1997, GENE CHROMOSOME CANC, V20, P372, DOI 10.1002/(SICI)1098-2264(199712)20:4<372::AID-GCC8>3.0.CO
[4]  
2-Z
[5]  
Bärlund M, 2000, CANCER RES, V60, P5340
[6]  
Corn PG, 1999, CANCER RES, V59, P3352
[7]  
Couch FJ, 1999, CANCER RES, V59, P1408
[8]   Amplification of DNA sequences from chromosome 19q13.1 in human pancreatic cell lines [J].
Curtis, LJ ;
Li, Y ;
Gerbault-Seureau, M ;
Kuick, R ;
Dutrillaux, AM ;
Goubin, G ;
Fawcett, J ;
Cram, S ;
Dutrillaux, B ;
Hanash, S ;
Muleris, M .
GENOMICS, 1998, 53 (01) :42-55
[9]  
Ding Y, 1999, DNA Res, V6, P347, DOI 10.1093/dnares/6.5.347
[10]   A bird's eye view of global methylation [J].
Eng, C ;
Herman, JG ;
Baylin, SB .
NATURE GENETICS, 2000, 24 (02) :101-102