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Genes usually encode proteins necessary for the proper functioning of a healthy cell. Mutations can often cause changes to the gene expression pattern, thereby altering the phenotype.
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arrayMap 2014: an updated cancer genome resource.

Haoyang Cai1, Saumya Gupta2, Prisni Rath3

  • 1Institute of Molecular Life Sciences, University of Zurich, 8057 Zurich, Switzerland Swiss Institute of Bioinformatics, 8057 Zurich, Switzerland Center of Growth, Metabolism, and Aging, Key Laboratory of Bio-Resources and Eco-Environment, College of Life Sciences, Sichuan University, Chengdu 610064, Sichuan, China haoyang.cai@gmail.com.

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Summary
This summary is machine-generated.

The arrayMap database now offers over 64,000 cancer genomic datasets for public access. This updated resource enhances data mining for somatic copy number aberrations (CNA) across human malignancies.

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Area of Science:

  • Oncogenomics
  • Cancer Genomics
  • Bioinformatics

Background:

  • Somatic copy number aberrations (CNA) are common in cancer genomes.
  • arrayMap is a public resource for oncogenomic array data and CNA profiles.
  • The 2014 edition expands content and data mining capabilities.

Purpose of the Study:

  • To present the 2014 edition of arrayMap, an enhanced resource for cancer genomic data.
  • To provide access to over 64,000 pre-processed array datasets covering numerous human malignancies.
  • To improve data mining support and visualization tools for cancer genomic research.

Main Methods:

  • Assembled and integrated over 64,000 genomic array datasets from public repositories and additional sources.
  • Applied custom processing pipelines for data integration and CNA profile generation.
  • Upgraded online tools for flexible array data visualization and processing of user-provided datasets.
  • Mapped data to multiple human reference genome editions (UCSC hg18, GRCh37).

Main Results:

  • The 2014 arrayMap release contains over 64,000 genomic datasets representing approximately 250 tumor diagnoses.
  • Enhanced data integration with multiple human reference genome versions.
  • Improved online tools for data visualization and processing of non-public data.
  • Freely downloadable tumor CNA data is available to promote data mining.

Conclusions:

  • The updated arrayMap resource significantly enhances the study of somatic copy number aberrations in cancer.
  • Provides a comprehensive and accessible platform for cancer genomic data mining and exploration.
  • Facilitates research into complex genomic events like chromothripsis-like patterns.