Normalization of Illumina Infinium whole-genome SNP data improves copy number estimates and allelic intensity ratios

ABSTRACT: Illumina Infinium whole genome genotyping (WGG) arrays are increasingly being applied in cancer genomics to study gene copy number alterations and allele-specific aberrations such as loss-of-heterozygosity (LOH). Methods developed for normalization of WGG arrays have mostly focused on diploid, normal samples. However, for cancer samples genomic aberrations may confound normalization and data interpretation. Therefore, we examined the effects of the conventionally used normalization method for Illumina Infinium arrays when applied to cancer samples. We demonstrate an asymmetry in the detection of the two alleles for each SNP, which deleteriously influences both allelic proportions and copy number estimates. The asymmetry is caused by a remaining bias between the two dyes used in the Infini

ORGANISM(S): Homo sapiens

SUBMITTER: Ake Borg 

PROVIDER: E-GEOD-11977 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress