SNP500Cancer: a public resource for sequence validation, assay development, and frequency analysis for genetic variation in candidate genes
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Hugues Sicotte | Daniela S. Gerhard | Brian Staats | Robert Welch | Stephen J. Chanock | Meredith Yeager | Bernice R. Packer | Andrew Crenshaw | Andrew Eckert | Michael Beerman | Laura Burdett | Liqun Qi | Mekhala Acharya | Vinita Puri | D. Gerhard | S. Chanock | L. Qi | M. Yeager | R. Welch | B. Staats | L. Burdett | A. Crenshaw | V. Puri | H. Sicotte | Andrew Eckert | M. Beerman | M. Acharya
[1] K. Buetow. Cyberinfrastructure: Empowering a "Third Way" in Biomedical Research , 2005, Science.
[2] Elizabeth M. Smigielski,et al. dbSNP: the NCBI database of genetic variation , 2001, Nucleic Acids Res..
[3] Brian Staats,et al. SNP500Cancer: a public resource for sequence validation and assay development for genetic variation in candidate genes , 2004, Nucleic Acids Res..
[4] Toshihiro Tanaka. The International HapMap Project , 2003, Nature.
[5] Bernice R. Packer,et al. Widespread purifying selection at polymorphic sites in human protein-coding loci , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[6] S. Chanock,et al. Sequence analysis of the mannose-binding lectin (MBL2) gene reveals a high degree of heterozygosity with evidence of selection , 2004, Genes and Immunity.
[7] M. Ashburner,et al. Gene Ontology: tool for the unification of biology , 2000, Nature Genetics.
[8] Damian Smedley,et al. Ensembl 2005 , 2004, Nucleic Acids Res..
[9] Jeffrey Ross-Ibarra,et al. Genetic Data Analysis II. Methods for Discrete Population Genentic Data , 2002 .
[10] N. Rothman,et al. Comparison of yield and genotyping performance of multiple displacement amplification and OmniPlex™ whole genome amplified DNA generated from multiple DNA sources , 2005, Human mutation.
[11] Mark Daly,et al. Haploview: analysis and visualization of LD and haplotype maps , 2005, Bioinform..
[12] Hugues Sicotte,et al. Genewindow: an interactive tool for visualization of genomic variation , 2005, Nature Genetics.
[13] S Rozen,et al. Primer3 on the WWW for general users and for biologist programmers. , 2000, Methods in molecular biology.
[14] Daniel O. Stram,et al. Modeling and E-M Estimation of Haplotype-Specific Relative Risks from Genotype Data for a Case-Control Study of Unrelated Individuals , 2003, Human Heredity.
[15] Jonathan Scott Friedlaender,et al. A Human Genome Diversity Cell Line Panel , 2002, Science.
[16] Richard Wooster,et al. Sequence-based cancer genomics: progress, lessons and opportunities , 2003, Nature Reviews Genetics.
[17] C. Carlson,et al. Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium. , 2004, American journal of human genetics.
[18] Robert Welch,et al. Effects of Natural Selection on Interpopulation Divergence at Polymorphic Sites in Human Protein-Coding Loci , 2005, Genetics.
[19] Tatiana A. Tatusova,et al. Entrez Gene: gene-centered information at NCBI , 2004, Nucleic Acids Res..
[20] Stephen J Chanock,et al. Genetic variation, nucleotide diversity, and linkage disequilibrium in seven telomere stability genes suggest that these genes may be under constraint , 2005, Human mutation.