A multilevel model to address batch effects in copy number estimation using SNP arrays

Quantifying uncertainty in genotype calls

(2009) Benilton S. Carvalho et al.   BIOINFORMATICS

Identification of Potential Driver Genes in Human Liver Carcinoma by Genomewide Screening

(2009) H. G. Woo et al.   CANCER RESEARCH

MMP13, Birc2 (cIAP1), and Birc3 (cIAP2), Amplified on Chromosome 9, Collaborate with p53 Deficiency in Mouse Osteosarcoma Progression

(2009) O. Ma et al.   CANCER RESEARCH

IncreasedMETGene Copy Number Negatively Affects Survival of Surgically Resected Non–Small-Cell Lung Cancer Patients

(2009) Federico Cappuzzo et al.   JOURNAL OF CLINICAL ONCOLOGY

Genomic disorders ten years on

(2009) James R Lupski   Genome Medicine

Structural Variation of Chromosomes in Autism Spectrum Disorder

(2008) Christian R. Marshall et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Hidden Markov models for the assessment of chromosomal alterations using high-throughput SNP arrays

(2008) Robert B. Scharpf et al.   Annals of Applied Statistics

Estimating Genome-Wide Copy Number Using Allele-Specific Mixture Models

(2008) Wenyi Wang et al.   JOURNAL OF COMPUTATIONAL BIOLOGY

Mapping and sequencing of structural variation from eight human genomes

(2008) Jeffrey M. Kidd et al.   NATURE

Integrated detection and population-genetic analysis of SNPs and copy number variation

(2008) Steven A McCarroll et al.   NATURE GENETICS

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

(2008) Joshua M Korn et al.   NATURE GENETICS