ID
44998
Descrizione
Principal Investigator: Ulrike Peters, PhD, Fred Hutchinson Cancer Research Center, Seattle, WA, USA MeSH: Colorectal Neoplasms,Sequence Analysis, DNA https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000410 This project was designed to use next generation sequencing technology to screen the protein coding regions of the genome for low frequency variants in a panel of high-risk colorectal adenocarcinoma cases. Blood and cell-line DNA for colorectal cancer patients and a subset of quality control samples that had existing whole exome sequence data were analyzed using Illumina HiSeq sequencers. Samples from this project were from participants in the Women's Health Initiative (WHI) and the Diet, Activity, and Lifestyle Study (DALS).
collegamento
https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000410
Keywords
versioni (2)
- 01/07/22 01/07/22 - Dr. Christian Niklas
- 12/10/22 12/10/22 - Adrian Schulz
Titolare del copyright
Ulrike Peters, PhD, Fred Hutchinson Cancer Research Center, Seattle, WA, USA
Caricato su
1 luglio 2022
DOI
Per favore, per richiedere un accesso.
Licenza
Creative Commons BY 4.0
Commenti del modello :
Puoi commentare il modello dati qui. Tramite i fumetti nei gruppi di articoli e articoli è possibile aggiungere commenti a quelli in modo specifico.
Commenti del gruppo di articoli per :
Commenti dell'articolo per :
Per scaricare i modelli di dati devi essere registrato. Per favore accesso o registrati GRATIS.
dbGaP phs000410 Whole Exome Sequencing for Colorectal Cancer
Subject ID, subject source, subject source ID, consent group and affection status of participants involved in the " Whole Exome Sequencing for Colorectal Cancer" project.
- StudyEvent: SEV1
- Eligibility Criteria
- Subject ID, subject source, subject source ID, consent group and affection status of participants involved in the " Whole Exome Sequencing for Colorectal Cancer" project.
- Sample ID, subject ID, sample sources, sample source ID, and IDs of samples used for whole exome sequencing and obtained from participants involved in the " Whole Exome Sequencing for Colorectal Cancer" project.
- Subject ID, case or control status, age, race, sex, and family history of colorectal cancer among participants involved in the "Whole Exome Sequencing for Colorectal Cancer" project.
- Sample ID, analyte type, body site where from samples were collected, type of samples including tumor or normal tissue, histological type of samples obtained from participants involved in the "Whole Exome Sequencing for Colorectal Cancer" project.
Similar models
Subject ID, subject source, subject source ID, consent group and affection status of participants involved in the " Whole Exome Sequencing for Colorectal Cancer" project.
- StudyEvent: SEV1
- Eligibility Criteria
- Subject ID, subject source, subject source ID, consent group and affection status of participants involved in the " Whole Exome Sequencing for Colorectal Cancer" project.
- Sample ID, subject ID, sample sources, sample source ID, and IDs of samples used for whole exome sequencing and obtained from participants involved in the " Whole Exome Sequencing for Colorectal Cancer" project.
- Subject ID, case or control status, age, race, sex, and family history of colorectal cancer among participants involved in the "Whole Exome Sequencing for Colorectal Cancer" project.
- Sample ID, analyte type, body site where from samples were collected, type of samples including tumor or normal tissue, histological type of samples obtained from participants involved in the "Whole Exome Sequencing for Colorectal Cancer" project.
C1257890 (UMLS CUI [1,2])
C0681850 (UMLS CUI [1,2])
C0449416 (UMLS CUI [1,2])
C0681850 (UMLS CUI [1,3])
C0449438 (UMLS CUI [1,2])
C0009932 (UMLS CUI [2,1])
C0449438 (UMLS CUI [2,2])