ArticleBMC bioinformatics2017
iGC-an integrated analysis package of gene expression and copy number alteration.
Article in BMC bioinformatics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.
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Who cites it
13 citing papers in PubMed.
- Functional genomics and tumor microenvironment analysis reveal prognostic biological subtypes in Mantle cell lymphoma.Nature communications · 2025Article
- A review on multi-omics integration for aiding study design of large scale TCGA cancer datasets.BMC genomics · 2025Review
- Functional Copy-Number Alterations as Diagnostic and Prognostic Biomarkers in Neuroendocrine Tumors.International journal of molecular sciences · 2024Article
- Mutational landscape of HSP family on human breast cancer.Scientific reports · 2024Article
- Machine Learning Methods for Gene Selection in Uveal Melanoma.International journal of molecular sciences · 2024Article
- MOPA: An integrative multi-omics pathway analysis method for measuring omics activity.PloS one · 2023Article
- Multi-Omics Analysis Reveals Clinical Value and Possible Mechanisms of ATAD1 Down-Regulation in Human Prostate Adenocarcinoma.Life (Basel, Switzerland) · 2022Article
- High prevalence of APOA1/C3/A4/A5 alterations in luminal breast cancers among young women in East Asia.NPJ breast cancer · 2021Article
- A comparative study of multi-omics integration tools for cancer driver gene identification and tumour subtyping.Briefings in bioinformatics · 2020Article
- DriverDBv3: a multi-omics database for cancer driver gene research.Nucleic acids research · 2020Article
- Multi-Omics Approaches to Improve Mitochondrial Disease Diagnosis: Challenges, Advances, and Perspectives.Frontiers in molecular biosciences · 2020Review
- Identification of candidate cancer drivers by integrative Epi-DNA and Gene Expression (iEDGE) data analysis.Scientific reports · 2019Article
- Integrated landscape of copy number variation and RNA expression associated with nodal metastasis in invasive ductal breast carcinoma.Oncotarget · 2018Article
Corrections and comments
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Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundWith the advancement in high-throughput technologies, researchers can simultaneously investigate gene expression and copy number alteration (CNA) data from individual patients at a lower cost. Traditional analysis methods analyze each type of data individually and integrate their results using Venn diagrams. Challenges arise, however, when the results are irreproducible and inconsistent across multiple platforms. To address these issues, one possible approach is to concurrently analyze both gene expression profiling and CNAs in the same individual.
resultsWe have developed an open-source R/Bioconductor package (iGC). Multiple input formats are supported and users can define their own criteria for identifying differentially expressed genes driven by CNAs. The analysis of two real microarray datasets demonstrated that the CNA-driven genes identified by the iGC package showed significantly higher Pearson correlation coefficients with their gene expression levels and copy numbers than those genes located in a genomic region with CNA. Compared with the Venn diagram approach, the iGC package showed better performance.
conclusionThe iGC package is effective and useful for identifying CNA-driven genes. By simultaneously considering both comparative genomic and transcriptomic data, it can provide better understanding of biological and medical questions. The iGC package's source code and manual are freely available at https://www.bioconductor.org/packages/release/bioc/html/iGC.html .
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