ID

45410

Beskrivning

Principal Investigator: Ashley Hill, MD, Children's National Medical Center, Washington, DC, USA MeSH: Pleuropulmonary blastoma https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000543 Pleuropulmonary blastoma (PPB) is a rare, aggressive pediatric cancer arising from the lung or pleural cavity. In this study, we sequenced and analyzed the exomes of 15 PPB matched tumor and normal pairs. This study is part of a larger effort to characterize pediatric cancers as part of the Slim Initiative for Genomic Medicine (SIGMA) project.

Länk

dbGap-study=phs000543

Nyckelord

  1. 2022-11-19 2022-11-19 - Chiara Middel
Rättsinnehavare

Ashley Hill, MD, Children's National Medical Center, Washington, DC, USA

Uppladdad den

19 november 2022

DOI

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Licens

Creative Commons BY 4.0

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dbGaP phs000543 Exome Sequencing of Pleuropulmonary Blastoma

Sample ID, subject ID, and sample use variables obtained from participants with pleuropulmonary blastoma and involved in the "Genomic Sequencing of Pleuropulmonary blastoma" project.

pht002937
Beskrivning

pht002937

Alias
UMLS CUI [1,1]
C3846158
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. Seq_DNA_SNP_MAF_Ind: Sample(s) were used to generate aggregate mutation annotation file (.maf) with individual SNP genotypes; Seq_DNA_WholeExome: Whole exome sequencing
Beskrivning

SAMPLE_USE

Datatyp

text

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

Similar models

Sample ID, subject ID, and sample use variables obtained from participants with pleuropulmonary blastoma and involved in the "Genomic Sequencing of Pleuropulmonary blastoma" project.

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
pht002937
C3846158 (UMLS CUI [1,1])
SUBJID
Item
Subject ID
string
C2348585 (UMLS CUI [1,1])
SAMPID
Item
Sample ID
string
C1299222 (UMLS CUI [1,1])
SAMPLE_USE
Item
Sample use. Seq_DNA_SNP_MAF_Ind: Sample(s) were used to generate aggregate mutation annotation file (.maf) with individual SNP genotypes; Seq_DNA_WholeExome: Whole exome sequencing
text
C2347026 (UMLS CUI [1,1])
C1524063 (UMLS CUI [1,2])

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