ArticleBioinformatics (Oxford, England)2011
BACOM: in silico detection of genomic deletion types and correction of normal cell contamination in copy number data.
Article in Bioinformatics (Oxford, England), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.
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16 citing papers in PubMed, 35 citations in OpenAlex.
- Obtaining spatially resolved tumor purity maps using deep multiple instance learning in a pan-cancer study.Patterns (New York, N.Y.) · 2022Article
- MFCNV: A New Method to Detect Copy Number Variations From Next-Generation Sequencing Data.Frontiers in genetics · 2020Article
- Accurate Inference of Tumor Purity and Absolute Copy Numbers From High-Throughput Sequencing Data.Frontiers in genetics · 2020Article
- DBS: a fast and informative segmentation algorithm for DNA copy number analysis.BMC bioinformatics · 2019Article
- Article
- BACOM2.0 facilitates absolute normalization and quantification of somatic copy number alterations in heterogeneous tumor.Scientific reports · 2015Article
- UNDO: a Bioconductor R package for unsupervised deconvolution of mixed gene expressions in tumor samples.Bioinformatics (Oxford, England) · 2015Article
- MethylPurify: tumor purity deconvolution and differential methylation detection from single tumor DNA methylomes.Genome biology · 2014Article
- AbsCN-seq: a statistical method to estimate tumor purity, ploidy and absolute copy numbers from next-generation sequencing data.Bioinformatics (Oxford, England) · 2014Article
- AISAIC: a software suite for accurate identification of significant aberrations in cancers.Bioinformatics (Oxford, England) · 2014Article
- A mixture model for expression deconvolution from RNA-seq in heterogeneous tissues.BMC bioinformatics · 2013Article
- PurityEst: estimating purity of human tumor samples using next-generation sequencing data.Bioinformatics (Oxford, England) · 2012Article
- Genome-wide identification of significant aberrations in cancer genome.BMC genomics · 2012Article
- Comparative analysis of methods for identifying recurrent copy number alterations in cancer.PloS one · 2012Article
- TAGCNA: a method to identify significant consensus events of copy number alterations in cancer.PloS one · 2012Article
- Integration of Network Biology and Imaging to Study Cancer Phenotypes and Responses.IEEE/ACM transactions on computational biology and bioinformaticsArticle
Corrections and comments
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Authors and funding
6 authors at 3 institutions in 1 country.
Funding
Abstract
motivationIdentification of somatic DNA copy number alterations (CNAs) and significant consensus events (SCEs) in cancer genomes is a main task in discovering potential cancer-driving genes such as oncogenes and tumor suppressors. The recent development of SNP array technology has facilitated studies on copy number changes at a genome-wide scale with high resolution. However, existing copy number analysis methods are oblivious to normal cell contamination and cannot distinguish between contributions of cancerous and normal cells to the measured copy number signals. This contamination could significantly confound downstream analysis of CNAs and affect the power to detect SCEs in clinical samples.
resultsWe report here a statistically principled in silico approach, Bayesian Analysis of COpy number Mixtures (BACOM), to accurately estimate genomic deletion type and normal tissue contamination, and accordingly recover the true copy number profile in cancer cells. We tested the proposed method on two simulated datasets, two prostate cancer datasets and The Cancer Genome Atlas high-grade ovarian dataset, and obtained very promising results supported by the ground truth and biological plausibility. Moreover, based on a large number of comparative simulation studies, the proposed method gives significantly improved power to detect SCEs after in silico correction of normal tissue contamination. We develop a cross-platform open-source Java application that implements the whole pipeline of copy number analysis of heterogeneous cancer tissues including relevant processing steps. We also provide an R interface, bacomR, for running BACOM within the R environment, making it straightforward to include in existing data pipelines. AVAILABILITY: The cross-platform, stand-alone Java application, BACOM, the R interface, bacomR, all source code and the simulation data used in this article are freely available at authors' web site: http://www.cbil.ece.vt.edu/software.htm.
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.