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Priyanka Dhingra

Researcher at Cornell University

Publications -  22
Citations -  2068

Priyanka Dhingra is an academic researcher from Cornell University. The author has contributed to research in topics: Gene & Cancer. The author has an hindex of 11, co-authored 14 publications receiving 1140 citations. Previous affiliations of Priyanka Dhingra include Indian Institute of Technology Delhi & Indian Institutes of Technology.

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Pan-cancer analysis of whole genomes

Peter J. Campbell, +1332 more
- 06 Feb 2020 - 
TL;DR: The flagship paper of the ICGC/TCGA Pan-Cancer Analysis of Whole Genomes Consortium describes the generation of the integrative analyses of 2,658 whole-cancer genomes and their matching normal tissues across 38 tumour types, the structures for international data sharing and standardized analyses, and the main scientific findings from across the consortium studies.
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Integrative pathway enrichment analysis of multivariate omics data

Marta Paczkowska, +132 more
- 01 Jan 2020 - 
TL;DR: The authors develop ActivePathways method, which uses data fusion techniques for integrative pathway analysis of multi-omics data and candidate gene discovery that discovers significantly enriched pathways across multiple datasets using statistical data fusion.
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Pathway and network analysis of more than 2500 whole cancer genomes

TL;DR: In this article, the authors performed multi-faceted pathway and network analyses of non-coding mutations across 2583 whole cancer genomes from 27 tumor types compiled by the ICGC/TCGA Pan-Cancer Analysis of Whole Genomes (PCAWG) Consortium, which aggregated whole genome sequencing data from 2658 cancer across 38 tumor types.
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Identification of Cancer Drivers at CTCF Insulators in 1,962 Whole Genomes

TL;DR: This study reveals several CTCF insulators as putative cancer drivers, and finds that alterations at two of the most frequently mutated regions in this insulator increase cell growth by 40%-50%, supporting the role of this boundary element as a cancer driver.
Posted ContentDOI

Discovery and characterization of coding and non-coding driver mutations in more than 2,500 whole cancer genomes

Esther Rheinbay, +74 more
- 23 Dec 2017 - 
TL;DR: These analyses redefine the landscape of non-coding driver mutations in cancer genomes, confirming a few previously reported elements and raising doubts about others, while identifying novel candidate elements across 27 cancer types.