Quantification of Normal Cell Fraction and Copy Number Neutral LOH in Clinical Lung Cancer Samples Using SNP Array Data
Open Access
- 26 June 2009
- journal article
- research article
- Published by Public Library of Science (PLoS) in PLOS ONE
- Vol. 4 (6) , e6057
- https://doi.org/10.1371/journal.pone.0006057
Abstract
Technologies based on DNA microarrays have the potential to provide detailed information on genomic aberrations in tumor cells. In practice a major obstacle for quantitative detection of aberrations is the heterogeneity of clinical tumor tissue. Since tumor tissue invariably contains genetically normal stromal cells, this may lead to a failure to detect aberrations in the tumor cells. Using SNP array data from 44 non-small cell lung cancer samples we have developed a bioinformatic algorithm that accurately models the fractions of normal and tumor cells in clinical tumor samples. The proportion of normal cells in combination with SNP array data can be used to detect and quantify copy number neutral loss-of-heterozygosity (CNNLOH) in the tumor cells both in crude tumor tissue and in samples enriched for tumor cells by laser capture microdissection. Genome-wide quantitative analysis of CNNLOH using the CNNLOH Quantifier method can help to identify recurrent aberrations contributing to tumor development in clinical tumor samples. In addition, SNP-array based analysis of CNNLOH may become important for detection of aberrations that can be used for diagnostic and prognostic purposes.Keywords
This publication has 21 references indexed in Scilit:
- A Hidden Markov Model to estimate population mixture and allelic copy-numbers in cancers using Affymetrix SNP arraysBMC Bioinformatics, 2007
- Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arraysGenome Research, 2006
- PLASQ: a generalized linear model-based procedure to determine allelic dosage in cancer cells from SNP array dataBiostatistics, 2006
- CARAT: A novel method for allelic detection of DNA copy number changes using high density oligonucleotide arraysBMC Bioinformatics, 2006
- Allele-Specific Amplification in Cancer Revealed by SNP Array AnalysisPLoS Computational Biology, 2005
- Exploring the tumour environment: cancer-associated fibroblasts as targets in cancer therapyEmerging Therapeutic Targets, 2005
- Allelic dosage analysis with genotyping microarraysBiochemical and Biophysical Research Communications, 2005
- A Robust Algorithm for Copy Number Detection Using High-Density Oligonucleotide Single Nucleotide Polymorphism Genotyping ArraysCancer Research, 2005
- An Integrated View of Copy Number and Allelic Alterations in the Cancer Genome Using Single Nucleotide Polymorphism ArraysCancer Research, 2004
- dChipSNP: significance curve and clustering of SNP-array-based loss-of-heterozygosity dataBioinformatics, 2004