Generating linkage mapping files from Affymetrix SNP chip data
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[1] M. Bahlo,et al. A novel splice site mutation in EYA4 causes DFNA10 hearing loss , 2007, American journal of medical genetics. Part A.
[2] M. Bahlo,et al. Keipert syndrome (Nasodigitoacoustic syndrome) is X‐linked and maps to Xq22.2–Xq28 , 2007, American journal of medical genetics. Part A.
[3] L Sun,et al. Statistical tests for detection of misspecified relationships by use of genome-screen data. , 2000, American journal of human genetics.
[4] G. Abecasis,et al. Merlin—rapid analysis of dense genetic maps using sparse gene flow trees , 2002, Nature Genetics.
[5] Zhaohui S. Qin,et al. A second generation human haplotype map of over 3.1 million SNPs , 2007, Nature.
[6] Peter J. Nürnberg,et al. ALOHOMORA: a tool for linkage analysis using 10K SNP array data , 2005, Bioinform..
[7] M. Bahlo,et al. Molecular characterization of a novel X‐linked syndrome involving developmental delay and deafness , 2007, American journal of medical genetics. Part A.
[8] Daniel J Schaid,et al. Caution on pedigree haplotype inference with software that assumes linkage equilibrium. , 2002, American journal of human genetics.
[9] Elizabeth A. Thompson,et al. Statistical inference from genetic data on pedigrees , 2003 .
[10] D. Stephan,et al. A novel splice site mutation in the RDX gene causes DFNB24 hearing loss in an Iranian family , 2009, American journal of medical genetics. Part A.
[11] M S McPeek,et al. Optimal allele‐sharing statistics for genetic mapping using affected relatives , 1999, Genetic epidemiology.
[12] Rafael A Irizarry,et al. Exploration, normalization, and genotype calls of high-density oligonucleotide SNP array data. , 2006, Biostatistics.
[13] Hitoshi Miyazawa,et al. Homozygosity haplotype allows a genomewide search for the autosomal segments shared among patients. , 2007, American journal of human genetics.
[14] M. Bahlo,et al. Cochlear Implants for DFNA17 Deafness , 2006, The Laryngoscope.
[15] Gudmundur A. Thorisson,et al. The International HapMap Project Web site. , 2005, Genome research.
[16] Pak Chung Sham,et al. IGG: A tool to integrate GeneChips for genetic studies , 2007, Bioinform..
[17] Toshihiro Tanaka. The International HapMap Project , 2003, Nature.
[18] Manuel A. R. Ferreira,et al. PLINK: a tool set for whole-genome association and population-based linkage analyses. , 2007, American journal of human genetics.
[19] G. Abecasis,et al. Handling marker-marker linkage disequilibrium: pedigree analysis with clustered markers. , 2005, American journal of human genetics.
[20] David M. Evans,et al. Guidelines for genotyping in genomewide linkage studies: single-nucleotide-polymorphism maps versus microsatellite maps. , 2004, American journal of human genetics.
[21] Emily L. Webb,et al. SNPLINK: multipoint linkage analysis of densely distributed SNP data incorporating automated linkage disequilibrium removal , 2005, Bioinform..
[22] C. Lueck,et al. A new dominantly inherited pure cerebellar ataxia, SCA 30 , 2008, Journal of Neurology, Neurosurgery, and Psychiatry.
[23] Gregory Leibon,et al. A SNP Streak Model for the Identification of Genetic Regions Identical-by-descent , 2008, Statistical applications in genetics and molecular biology.