Highly Sensitive Method for Genomewide Detection of Allelic Composition in Nonpaired, Primary Tumor Specimens by Use of Affymetrix Single-Nucleotide–Polymorphism Genotyping Microarrays

This publication has 28 references indexed in Scilit:

• High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping
  Genome Research, 2006
• Inferring Loss-of-Heterozygosity from Unpaired Tumors Using High-Density Oligonucleotide SNP Arrays
  PLoS Computational Biology, 2006
• Genome-Wide Analysis for Loss of Heterozygosity in Primary and Recurrent Phyllodes Tumor and Fibroadenoma of Breast using Single Nucleotide Polymorphism Arrays
  Breast Cancer Research and Treatment, 2006
• A Gain-of-Function Mutation ofJAK2in Myeloproliferative Disorders
  New England Journal of Medicine, 2005
• A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera
  Nature, 2005
• Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders
  The Lancet, 2005
• Genotyping over 100,000 SNPs on a pair of oligonucleotide arrays
  Nature Methods, 2004
• Concurrent analysis of loss of heterozygosity (LOH) and copy number abnormality (CNA) for oral premalignancy progression using the Affymetrix 10K SNP mapping array
  Human Genetics, 2004
• High-Resolution Analysis of DNA Copy Number Using Oligonucleotide Microarrays
  Genome Research, 2004
• Molecular characterization of the recurrent unbalanced translocation der(1;7)(q10;p10)
  Blood, 2003