ID

45506

Descrição

Principal Investigator: Matthew Meyerson, MD, PhD, Broad Institute, Cambridge MA, Dana Farber Cancer Institute, Boston MA, USA MeSH: Carcinoma, Non-Small-Cell Lung https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000488 Lung carcinoma is the leading cause of cancer death in the United States and world-wide; lung adenocarcinoma is the most common cause of lung cancer. Pilot studies of lung adenocarcinoma with hybrid-capture based whole exome sequencing will enable us to identify new targets for therapy and improve diagnosis. We will analyze a blend of whole exome and whole genome sequencing data as well as copy number and somatic mutation calls for 200 tumor and matched normal controls. When completed this study will represent the most comprehensive lung adenocarcinoma genome dataset to date.

Link

dbGap study = phs000488

Palavras-chave

  1. 09/11/2022 09/11/2022 - Dr. med. Lucy Kessler
  2. 13/12/2022 13/12/2022 - Kristina Keller
Titular dos direitos

Matthew Meyerson, MD, PhD, Broad Institute, Cambridge MA, Dana Farber Cancer Institute, Boston MA, USA

Transferido a

13 de dezembro de 2022

DOI

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Licença

Creative Commons BY 4.0

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dbGaP phs000488 Genomic Sequencing of Lung Adenocarcinoma

Sample ID, subject ID, and sample use variables obtained from participants with lung adenocarcinoma and involved in the "Genomic Sequencing of Lung Adenocarcinoma" project.

pht002910
Descrição

pht002910

Alias
UMLS CUI [1,1]
C0370003
UMLS CUI [1,2]
C0600091
UMLS CUI [2,1]
C0200345
UMLS CUI [2,2]
C0457083
Subject ID
Descrição

SUBJECT_ID

Tipo de dados

string

Alias
UMLS CUI [1,1]
C2348584
Sample ID
Descrição

SAMPLE_ID

Tipo de dados

string

Alias
UMLS CUI [1,1]
C1299222
Sample use. Array_SNP: SNP genotypes obtained using standard or custom microarrays; Seq_DNA_WholeExome: Whole exome sequencing; Seq_DNA_WholeGenome: Whole genome sequencing
Descrição

SAMPLE_USE

Tipo de dados

text

Alias
UMLS CUI [1,1]
C0370003
UMLS CUI [1,2]
C4027253
UMLS CUI [1,3]
C0022885

Similar models

Sample ID, subject ID, and sample use variables obtained from participants with lung adenocarcinoma and involved in the "Genomic Sequencing of Lung Adenocarcinoma" project.

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
pht002910
C0370003 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
C0200345 (UMLS CUI [2,1])
C0457083 (UMLS CUI [2,2])
SUBJECT_ID
Item
Subject ID
string
C2348584 (UMLS CUI [1,1])
SAMPLE_ID
Item
Sample ID
string
C1299222 (UMLS CUI [1,1])
SAMPLE_USE
Item
Sample use. Array_SNP: SNP genotypes obtained using standard or custom microarrays; Seq_DNA_WholeExome: Whole exome sequencing; Seq_DNA_WholeGenome: Whole genome sequencing
text
C0370003 (UMLS CUI [1,1])
C4027253 (UMLS CUI [1,2])
C0022885 (UMLS CUI [1,3])

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