Genomics

Dataset Information

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National Human Genome Research Institute Tumor Sequencing Project (TSP) - Lung Adenocarcinoma


ABSTRACT:

The Tumor Sequencing Project (TSP) Consortium is a collaboration among participants at the Baylor College of Medicine Human Genome Sequencing Center, the Broad Institute Genome Sequencing Platform, the Dana Farber Cancer Institute, the Memorial Sloan-Kettering Cancer Center, the Genome Sequencing Center and Siteman Cancer Center at Washington University, the M.D. Anderson Cancer Center and the University of Michigan Medical Center. The TSP Part A will pilot approaches to large-scale identification of genomic changes in tumors by sequencing the exonic regions of 623 genes in 188 specimens of adenocarcinoma of the lung, as well as using high density SNP genotyping arrays for high resolution identification of changes in chromosomal copy number.

The TSP Part B will pilot approaches to tumor characterization of lung adenocarcinoma samples using next-generation sequencing technologies and benchmark those results against Part A data generated with ABI3730 instruments.

OTHER RELATED OMICS DATASETS IN: PRJNA74925PRJNA41441PRJNA112737

PROVIDER: phs000144.v1.p1 | EGA |

REPOSITORIES: EGA

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Publications

Somatic mutations affect key pathways in lung adenocarcinoma.

Ding Li L   Getz Gad G   Wheeler David A DA   Mardis Elaine R ER   McLellan Michael D MD   Cibulskis Kristian K   Sougnez Carrie C   Greulich Heidi H   Muzny Donna M DM   Morgan Margaret B MB   Fulton Lucinda L   Fulton Robert S RS   Zhang Qunyuan Q   Wendl Michael C MC   Lawrence Michael S MS   Larson David E DE   Chen Ken K   Dooling David J DJ   Sabo Aniko A   Hawes Alicia C AC   Shen Hua H   Jhangiani Shalini N SN   Lewis Lora R LR   Hall Otis O   Zhu Yiming Y   Mathew Tittu T   Ren Yanru Y   Yao Jiqiang J   Scherer Steven E SE   Clerc Kerstin K   Metcalf Ginger A GA   Ng Brian B   Milosavljevic Aleksandar A   Gonzalez-Garay Manuel L ML   Osborne John R JR   Meyer Rick R   Shi Xiaoqi X   Tang Yuzhu Y   Koboldt Daniel C DC   Lin Ling L   Abbott Rachel R   Miner Tracie L TL   Pohl Craig C   Fewell Ginger G   Haipek Carrie C   Schmidt Heather H   Dunford-Shore Brian H BH   Kraja Aldi A   Crosby Seth D SD   Sawyer Christopher S CS   Vickery Tammi T   Sander Sacha S   Robinson Jody J   Winckler Wendy W   Baldwin Jennifer J   Chirieac Lucian R LR   Dutt Amit A   Fennell Tim T   Hanna Megan M   Johnson Bruce E BE   Onofrio Robert C RC   Thomas Roman K RK   Tonon Giovanni G   Weir Barbara A BA   Zhao Xiaojun X   Ziaugra Liuda L   Zody Michael C MC   Giordano Thomas T   Orringer Mark B MB   Roth Jack A JA   Spitz Margaret R MR   Wistuba Ignacio I II   Ozenberger Bradley B   Good Peter J PJ   Chang Andrew C AC   Beer David G DG   Watson Mark A MA   Ladanyi Marc M   Broderick Stephen S   Yoshizawa Akihiko A   Travis William D WD   Pao William W   Province Michael A MA   Weinstock George M GM   Varmus Harold E HE   Gabriel Stacey B SB   Lander Eric S ES   Gibbs Richard A RA   Meyerson Matthew M   Wilson Richard K RK  

Nature 20081001 7216


Determining the genetic basis of cancer requires comprehensive analyses of large collections of histopathologically well-classified primary tumours. Here we report the results of a collaborative study to discover somatic mutations in 188 human lung adenocarcinomas. DNA sequencing of 623 genes with known or potential relationships to cancer revealed more than 1,000 somatic mutations across the samples. Our analysis identified 26 genes that are mutated at significantly high frequencies and thus ar  ...[more]

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