Whole-Genome Amplification Enables Accurate Genotyping for Microarray-Based High-Density Single Nucleotide Polymorphism Array
暂无分享,去创建一个
Muhammad G. Kibriya | Jenny Chang-Claude | Habibul Ahsan | J. Chang-Claude | E. John | F. Jasmine | M. Kibriya | H. Ahsan | I. Andrulis | Irene L. Andrulis | Esther M. John | Farzana Jasmine
[1] S. Kingsmore,et al. Comprehensive human genome amplification using multiple displacement amplification , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[2] Carolyn J. Brown,et al. A comprehensive analysis of common copy-number variations in the human genome. , 2007, American journal of human genetics.
[3] Vladimir Makarov,et al. Two methods of whole-genome amplification enable accurate genotyping across a 2320-SNP linkage panel. , 2004, Genome research.
[4] A. Syvänen,et al. Quantitative evaluation by minisequencing and microarrays reveals accurate multiplexed SNP genotyping of whole genome amplified DNA. , 2003, Nucleic acids research.
[5] Norman Boyd,et al. The Breast Cancer Family Registry: an infrastructure for cooperative multinational, interdisciplinary and translational studies of the genetic epidemiology of breast cancer , 2004, Breast Cancer Research.
[6] V G Cheung,et al. Whole genome amplification using a degenerate oligonucleotide primer allows hundreds of genotypes to be performed on less than one nanogram of genomic DNA. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[7] N. Carter,et al. Degenerate oligonucleotide-primed PCR: general amplification of target DNA by a single degenerate primer. , 1992, Genomics.
[8] Sonja W. Scholz,et al. Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals. , 2007, Human molecular genetics.
[9] A. Ashworth,et al. Array CGH using whole genome amplification of fresh-frozen and formalin-fixed, paraffin-embedded tumor DNA. , 2006, Genomics.
[10] Nicholas G Martin,et al. Estimation of the Rate of SNP Genotyping Errors From DNA Extracted From Different Tissues , 2005, Twin Research and Human Genetics.
[11] D. Pinto,et al. Copy-number variation in control population cohorts. , 2007, Human molecular genetics.
[12] J. Delhanty,et al. Detailed chromosomal and molecular genetic analysis of single cells by whole genome amplification and comparative genomic hybridisation. , 1999, Nucleic acids research.
[13] Daniel Pinkel,et al. Whole genome analysis of genetic alterations in small DNA samples using hyperbranched strand displacement amplification and array-CGH. , 2003, Genome research.
[14] D. Conrad,et al. Global variation in copy number in the human genome , 2006, Nature.
[15] Gary D. Bader,et al. Germ-line DNA copy number variation frequencies in a large North American population , 2007, Human Genetics.
[16] Alan Mackay,et al. Evaluation of Phi29-based whole-genome amplification for microarray-based comparative genomic hybridisation , 2007, Laboratory Investigation.
[17] Mark B Gerstein,et al. Assessment of whole genome amplification-induced bias through high-throughput, massively parallel whole genome sequencing , 2006, BMC Genomics.
[18] R. Hubert,et al. Whole genome amplification from a single cell: implications for genetic analysis. , 1992, Proceedings of the National Academy of Sciences of the United States of America.
[19] Rameen Beroukhim,et al. Genome coverage and sequence fidelity of phi29 polymerase-based multiple strand displacement whole genome amplification. , 2004, Nucleic acids research.
[20] M. García-Closas,et al. Collection of buccal cell DNA using treated cards. , 2000, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.
[21] M. Daly,et al. A high-density screen for linkage in multiple sclerosis. , 2005, American journal of human genetics.
[22] S. Chanock,et al. Effects of DNA mass on multiple displacement whole genome amplification and genotyping performance , 2005, BMC biotechnology.
[23] Lawrence R. Rabiner,et al. A tutorial on hidden Markov models and selected applications in speech recognition , 1989, Proc. IEEE.
[24] J. Collinge,et al. Successful amplification of degraded DNA for use with high‐throughput SNP genotyping platforms , 2008, Human mutation.
[25] Roger S Lasken,et al. Unbiased whole-genome amplification directly from clinical samples. , 2003, Genome Research.
[26] J. Chang-Claude,et al. Breastfeeding and breast cancer risk by age 50 among women in Germany , 2000, Cancer Causes & Control.
[27] D. Hunter,et al. Multiple displacement amplification prior to single nucleotide polymorphism genotyping in epidemiologic studies , 2003, Biotechnology Letters.
[28] Roger S Lasken,et al. Whole genome amplification: abundant supplies of DNA from precious samples or clinical specimens. , 2003, Trends in biotechnology.
[29] Philippe Froguel,et al. Array CGH analysis of copy number variation identifies 1284 new genes variant in healthy white males: implications for association studies of complex diseases. , 2007, Human molecular genetics.
[30] J. Todd,et al. BMC Biotechnology BioMed Central Methodology article A gene expression system offering multiple levels of regulation: the Dual Drug Control (DDC) system , 2004 .
[31] A. Syvänen,et al. Multiple displacement amplification to create a long‐lasting source of DNA for genetic studies , 2006, Human mutation.
[32] L. Feuk,et al. Detection of large-scale variation in the human genome , 2004, Nature Genetics.