Forum: The Cancer Genome Atlas Research Network Symposium Meeting - 2011
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gravatar for Malachi Griffith
6.5 years ago by
Washington University School of Medicine, St. Louis, USA
Malachi Griffith17k wrote:

A who's who of cancer genomics and bioinformatics speakers discuss progress on the TCGA. Videos and slides for all 31 talks are provided. Also available as a video playlist of GenomeTV

From the NHGRI website:

In November 2011, The Cancer Genome Atlas (TCGA) Research Network held its first open scientific symposium in Washington, D.C. TCGA researchers and outside investigators from around the world presented results on the use of TCGA data to make biological discoveries about cancer. The two-day meeting included lectures, collaborative workshops and poster sessions. The lectures are made freely available here and on NHGRI's YouTube channel, GenomeTV.

The National Cancer Institute (NCI) and the National Human Genome Research Institute (NHGRI), two of the National Institutes of Health's 27 institutes and centers, jointly fund TCGA to use genome analysis technologies, including large-scale genome sequencing, to accelerate the understanding of the molecular basis of cancer.

Some specific talks selected for their bioinformatics content:

Predicting Patient Outcomes With Chained Biological Concept Classifiers

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Multi-Cancer Mutual Exclusivity Analysis of Genomic Alterations

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Integrate Analysis and Interactive Exploration of Data from TCGA

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Absolute Quantification of Somatic DNA Alterations in Cancer Reveals Frequent Genome Doublings in Human Cancers

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Algorithms for Automated Discovery of Mutated Pathways in Cancer

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An Integrated View Into Multivariate Associations Inferred From TCGA Cancer Data

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Patient-Specific Pathway Analysis Using PARADIGM Identifies Key Activities in Multiple Cancers

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Large-Scale Cancer Genomics Data Analysis

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RF-ACE for Uncovering Nonlinear Associations From Heterogeneous Cancer Data

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Uncovering the Pseudo-Subclonal Structure of Tumor Sample With Copy Number Variation Analysis of Next-Generation Sequencing Data

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Comparison and Validation of Somatic Mutation Callers

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