ID

45071

Description

Principal Investigator: Adam Bass, Broad Institute, Cambridge MA, Dana Farber Cancer Institute, Boston, MA, USA MeSH: Adenocarcinoma,Colonic Neoplasms https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000374 This study was the first-known effort to complete the complete genome sequencing of primary colorectal adenocarcinomas and the matched germline genome. Nine colorectal adenocarcinomas selected on the basis of having chromosomal instability were subjected to 'shotgun' Illumina sequencing with 101-bp paired end reads to an approximate goal of 30x coverage of tumor and of normal. From these sequences, we used various computational techniques to identify somatic point mutations, insertion/deletions and structural rearrangements in these tumors. From these data, we identified new insights into the rates of background mutations in these cancers, new spectrums of structural alterations including the identification of a novel in-frame fusion gene.

Lien

https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000374

Mots-clés

  1. 18/08/22 18/08/22 - Simon Heim
  2. 12/10/22 12/10/22 - Adrian Schulz
Détendeur de droits

Adam Bass, Broad Institute, Cambridge MA, Dana Farber Cancer Institute, Boston, MA, USA

Téléchargé le

18 agosto 2022

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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dbGaP phs000374 Genomic Sequencing of Colorectal Adenocarcinomas

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