Copy Number and Loss of Heterozygosity Detected by SNP Array of Formalin-Fixed Tissues Using Whole-Genome Amplification

The Mouse Genome Database (MGD): premier model organism resource for mammalian genomics and genetics

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Ensembl 2011

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COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer

(2010) S. A. Forbes et al.   NUCLEIC ACIDS RESEARCH

Quantifying uncertainty in genotype calls

(2009) Benilton S. Carvalho et al.   BIOINFORMATICS

Whole Genome Amplification for Array Comparative Genomic Hybridization Using DNA Extracted from Formalin-Fixed, Paraffin-Embedded Histological Sections

(2009) Jian Huang et al.   JOURNAL OF MOLECULAR DIAGNOSTICS

Genome-wide copy number alterations detection in fresh frozen and matched FFPE samples using SNP 6.0 arrays

(2008) Marianne Tuefferd et al.   GENES CHROMOSOMES & CANCER

High fidelity of whole-genome amplified DNA on high-density single nucleotide polymorphism arrays

(2008) Jinchuan Xing et al.   GENOMICS

Successful amplification of degraded DNA for use with high-throughput SNP genotyping platforms

(2008) Simon Mead et al.   HUMAN MUTATION

Fast unfolding of communities in large networks

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Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs

(2008) Joshua M Korn et al.   NATURE GENETICS

Impact of whole genome amplification on analysis of copy number variants

(2008) T. J. Pugh et al.   NUCLEIC ACIDS RESEARCH