A fast and accurate method to detect allelic genomic imbalances underlying mosaic rearrangements using SNP array data

R-Gada: a fast and flexible pipeline for copy number analysis in association studies

(2010) Roger Pique-Regi et al.   BMC BIOINFORMATICS

Detection of low-level mosaicism and placental mosaicism by oligonucleotide array comparative genomic hybridization

(2010) Stuart A Scott et al.   GENETICS IN MEDICINE

Mechanisms of mosaicism, chimerism and uniparental disomy identified by single nucleotide polymorphism array analysis

(2010) Laura K. Conlin et al.   HUMAN MOLECULAR GENETICS

Association of common copy number variants at the glutathione S-transferase genes and rare novel genomic changes with schizophrenia

(2009) B Rodríguez-Santiago et al.   MOLECULAR PSYCHIATRY

Origins and functional impact of copy number variation in the human genome

(2009) Donald F. Conrad et al.   NATURE

Sparse representation and Bayesian detection of genome copy number alterations from microarray data

(2008) Roger Pique-Regi et al.   BIOINFORMATICS

Somatic mosaicism for copy number variation in differentiated human tissues

(2008) Arkadiusz Piotrowski et al.   HUMAN MUTATION

Genomic Imbalances in Neonates With Birth Defects: High Detection Rates by Using Chromosomal Microarray Analysis

(2008) X.-Y. Lu et al.   PEDIATRICS

Segmentation-based detection of allelic imbalance and loss-of-heterozygosity in cancer cells using whole genome SNP arrays

(2008) Johan Staaf et al.   GENOME BIOLOGY