ID

45367

Beskrivning

Principal Investigator: Winnie S. Liang, PhD, Translational Genomics Research Institute, Phoenix, AZ, USA MeSH: Pancreatic Neoplasms,Carcinoma https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000550 In this study, we whole genome sequenced tumor/normal pairs from three pancreatic adenocarcinoma patients to separately characterize each patient with respect to somatic alterations. For 2 patients for whom tumor RNA was available, we also performed RNA sequencing to evaluate gene expression changes. While additional sequencing is needed to improve our understanding of the disease, the information acquired from this study contributes to our knowledge base on pancreatic cancer and helps to establish a foundation for identifying and developing more efficacious treatments for patients.

Länk

dbGap-study=phs000550

Nyckelord

  1. 2022-11-04 2022-11-04 - Chiara Middel
Rättsinnehavare

Winnie S. Liang, PhD, Translational Genomics Research Institute, Phoenix, AZ, USA

Uppladdad den

4 november 2022

DOI

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Licens

Creative Commons BY 4.0

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dbGaP phs000550 Characterization of Pancreatic Adenocarcinoma Patients Using NGS

Subject ID, sample ID, and sample use variable obtained from participants with pancreatic adenocarcinoma and involved in the "Genome-Wide Characterization of Pancreatic Adenocarcinoma Patients Using Next Generation Sequencing" project.

pht003128
Beskrivning

pht003128

Subject ID
Beskrivning

SUBJID

Datatyp

string

Alias
UMLS CUI [1,1]
C2348585
Sample ID
Beskrivning

SAMPID

Datatyp

string

Alias
UMLS CUI [1,1]
C1299222
Sample use
Beskrivning

SAMPLE_USE

Datatyp

text

Alias
UMLS CUI [1,1]
C1524063
UMLS CUI [1,2]
C2347026

Similar models

Subject ID, sample ID, and sample use variable obtained from participants with pancreatic adenocarcinoma and involved in the "Genome-Wide Characterization of Pancreatic Adenocarcinoma Patients Using Next Generation Sequencing" project.

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
pht003128
SUBJID
Item
Subject ID
string
C2348585 (UMLS CUI [1,1])
SAMPID
Item
Sample ID
string
C1299222 (UMLS CUI [1,1])
Item
Sample use
text
C1524063 (UMLS CUI [1,1])
C2347026 (UMLS CUI [1,2])
Code List
Sample use
CL Item
Whole genome sequencing data available through SRA (WGS_SRA)
CL Item
Whole transcriptome sequencing (WTS_SRA)

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