Evidence map›Paper›PMID 21498400›Full record

ArticleBioinformatics (Oxford, England)2011

BACOM: in silico detection of genomic deletion types and correction of normal cell contamination in copy number data.

Guoqiang Yu, Bai Zhang, G Steven Bova, Jianfeng Xu, Ie-Ming Shih, Yue Wang

Open access · bronzeAbstract readEvaluation Study
In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.1field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 35 citations in OpenAlex.

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  16. Integration of Network Biology and Imaging to Study Cancer Phenotypes and Responses.IEEE/ACM transactions on computational biology and bioinformatics
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 1 country.

Guoqiang YuBradley Department of Electrical and Computer Engineering, Virginia Polytechnic Institute and State University, Arlington, VA 22203, USA.
Bai Zhang
G Steven Bova
Jianfeng Xu
Ie-Ming Shih
Yue Wang
Johns Hopkins University · USVirginia Tech · USVirginia Tech - Wake Forest University School of Biomedical Engineering & Sciences · US

Funding

Molecular Diagnostics for Malignant EffusionR01CA103937 · NCI · JOHNS HOPKINS UNIVERSITY · PI SHIH, IE-MING · 2004 to 2012
$2.7M
The Roles of HBXAP Gene in Ovarian CancerR01CA129080 · NCI · JOHNS HOPKINS UNIVERSITY · PI SHIH, IE-MING · 2008 to 2012
$1.7M
Compute Decomposition/Composite Molecular SignaturesR33EB000830 · NIBIB · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI WANG, YUE · 2005 to 2007
$1.6M
Comprehensive Analysis of Microarray Gene ExpressionR33CA109872 · NCI · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI WANG, YUE · 2005 to 2007
$1.4M
Compute Decomposition/Composite Molecular SignaturesR21EB000830 · NIBIB · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI WANG, YUE · 2003 to 2004
$266k
Comprehensive Analysis of Microarray Gene ExpressionR21CA109872 · NCI · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI WANG, YUE · 2004 to 2004
$149k
NCI NIH HHS CA103937NCI NIH HHS CA109872NCI NIH HHS CA129080NIBIB NIH HHS EB000830
6 · The paper itself

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.

Indexed as

DNA Copy Number VariationsSequence DeletionSoftwareAlgorithmsBayes TheoremDNA, NeoplasmFemaleGenomicsHumansMaleMutationOligonucleotide Array Sequence AnalysisOvarian NeoplasmsPolymorphism, Single NucleotideProstatic NeoplasmsDNA, Neoplasm

Identifiers

PMID21498400
PMCPMC3102226
OpenAlexW2161266543

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.