Published online 9 July 2004
Nucleic Acids Research, Vol. 32 No. 12 © Oxford University Press 2004; all rights reserved
A set of BAC clones spanning the human genome
BC Cancer Agency Genome Sciences Center and 1 BC Cancer Agency, Vancouver, BC V5Z 4E6, Canada, 2 Department of Human Genetics, 417, University Medical Center Nijmegen, P.O. Box 9101, 6500 HB Nijmegen, The Netherlands, 3 Cancer Research Institute, Box 0808, University of California at San Francisco, San Francisco, CA 94143-0808, USA, 4 BACPAC Resources, Children's Hospital Oakland, 747 52nd Street, Oakland, CA 94609, USA and 5 The Institute for Genomic Research, 9712 Medical Center Drive, Rockville, MD 20850, USA
* To whom correspondence should be addressed. Tel: +1 604 877 6084; Fax: +1 604 877 6085; Email: mmarra{at}bcgsc.bc.ca
Received May 21, 2004; Revised and Accepted June 22, 2004
Using the human bacterial artificial chromosome (BAC) fingerprint-based physical map, genome sequence assembly and BAC end sequences, we have generated a fingerprint-validated set of 32 855 BAC clones spanning the human genome. The clone set provides coverage for at least 98% of the human fingerprint map, 99% of the current assembled sequence and has an effective resolving power of 79 kb. We have made the clone set publicly available, anticipating that it will generally facilitate FISH or array-CGH-based identification and characterization of chromosomal alterations relevant to disease.
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
G. Kirov, D. Gumus, W. Chen, N. Norton, L. Georgieva, M. Sari, M. C O'Donovan, F. Erdogan, M. J Owen, H.-H. Ropers, et al. Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia Hum. Mol. Genet., February 1, 2008; 17(3): 458 - 465. [Abstract] [Full Text] [PDF] |
||||
![]() |
K Osoegawa, G M Vessere, K H Utami, M A Mansilla, M K Johnson, B M Riley, J L'Heureux, R Pfundt, J Staaf, W A van der Vliet, et al. Identification of novel candidate genes associated with cleft lip and palate using array comparative genomic hybridisation J. Med. Genet., February 1, 2008; 45(2): 81 - 86. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. Shen, D. T. Miller, S. W. Cheung, V. Lip, X. Sheng, K. Tomaszewicz, H. Shao, H. Fang, H. S. Tang, M. Irons, et al. Development of a Focused Oligonucleotide-Array Comparative Genomic Hybridization Chip for Clinical Diagnosis of Genomic Imbalance Clin. Chem., December 1, 2007; 53(12): 2051 - 2059. [Abstract] [Full Text] [PDF] |
||||
![]() |
A C Karcanias, K Ichimura, M J Mitchell, C A Sargent, and N A Affara Analysis of sex chromosome abnormalities using X and Y chromosome DNA tiling path arrays J. Med. Genet., July 1, 2007; 44(7): 429 - 436. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Stjernqvist, T. Ryden, M. Skold, and J. Staaf Continuous-index hidden Markov modelling of array CGH copy number data Bioinformatics, April 15, 2007; 23(8): 1006 - 1014. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Y. Hehir-Kwa, M. Egmont-Petersen, I. M. Janssen, D. Smeets, A. G. van Kessel, and J. A. Veltman Genome-wide Copy Number Profiling on High-density Bacterial Artificial Chromosomes, Single-nucleotide Polymorphisms, and Oligonucleotide Microarrays: A Platform Comparison based on Statistical Power Analysis DNA Res, March 15, 2007; (2007) dsm002v1. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Gratias, H. Rieder, R. Ullmann, L. Klein-Hitpass, S. Schneider, R. Boloni, M. Kappler, and D. R. Lohmann Allelic Loss in a Minimal Region on Chromosome 16q24 Is Associated with Vitreous Seeding of Retinoblastoma Cancer Res., January 1, 2007; 67(1): 408 - 416. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. A. Veltman and B. B.A. de Vries Diagnostic Genome Profiling: Unbiased Whole Genome or Targeted Analysis? J. Mol. Diagn., November 1, 2006; 8(5): 534 - 537. [Full Text] [PDF] |
||||
![]() |
D. G. Albertson, A. M. Snijders, J. Fridlyand, R. Jordan, D. Pinkel, B. L. Schmidt, C. Baldwin, C. Garnis, L. Zhang, M. Rosin, et al. Genomic analysis of tumors by array comparative genomic hybridization: more is better. Cancer Res., April 1, 2006; 66(7): 3955 - 3956. [Full Text] [PDF] |
||||
![]() |
S. Volik, B. J. Raphael, G. Huang, M. R. Stratton, G. Bignel, J. Murnane, J. H. Brebner, K. Bajsarowicz, P. L. Paris, Q. Tao, et al. Decoding the fine-scale structure of a breast cancer genome and transcriptome Genome Res., March 1, 2006; 16(3): 394 - 404. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. M. Wilson, S. Flibotte, P. I. Missirlis, M. A. Marra, S. Jones, K. Thornton, A. G. Clark, and R. A. Holt Identification by full-coverage array CGH of human DNA copy number increases relative to chimpanzee and gorilla Genome Res., February 1, 2006; 16(2): 173 - 181. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. A. Kiemeney, R. P. Kuiper, R. Pfundt, S. van Reijmersdal, M. P. Schoenberg, K. K. Aben, M. F. Niermeijer, J. A. Witjes, and E. F.P.M. Schoenmakers No Evidence For Large-scale Germline Genomic Aberrations in Hereditary Bladder Cancer Patients with High-Resolution Array-Based Comparative Genomic Hybridization Cancer Epidemiol. Biomarkers Prev., January 1, 2006; 15(1): 180 - 183. [Full Text] [PDF] |
||||
![]() |
L. H.J. Looijenga, R. Hersmus, A. J.M. Gillis, R. Pfundt, H. J. Stoop, R. J.H.L.M. van Gurp, J. Veltman, H. B. Beverloo, E. van Drunen, A. Geurts van Kessel, et al. Genomic and Expression Profiling of Human Spermatocytic Seminomas: Primary Spermatocyte as Tumorigenic Precursor and DMRT1 as Candidate Chromosome 9 Gene Cancer Res., January 1, 2006; 66(1): 290 - 302. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Pavlicek, R. House, A. J. Gentles, J. Jurka, and B. E. Morrow Traffic of genetic information between segmental duplications flanking the typical 22q11.2 deletion in velo-cardio-facial syndrome/DiGeorge syndrome Genome Res., November 1, 2005; 15(11): 1487 - 1495. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. A. Shakes, D. M. Garland, D. K. Srivastava, K. R. Harewood, and P. K. Chatterjee Minimal cross-recombination between wild-type and loxP511 sites in vivo facilitates truncating both ends of large DNA inserts in pBACe3.6 and related vectors Nucleic Acids Res., August 1, 2005; 33(13): e118 - e118. [Abstract] [Full Text] [PDF] |
||||









