ID

45509

Descrição

Principal Investigator: Marie-Claude Gingras, PhD, Baylor College of Medicine, Human Genome Sequencing Center, Houston, TX, USA MeSH: Carcinoma, Hepatocellular https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000509 Hepatocellular carcinoma (HCC) accounts for 85-90% of primary liver cancers. We have focused on three major HCC etiologies:hepatitis C virus (HCV), hepatitis B virus (HBV), and nonviral causes. The onset and progression of cancer is driven by extensive rearrangement and mutation of the genome. We combined our capability to capture and enrich exome DNA with the next generation sequencing capacity to allow us to detect and characterize the somatic mutation profile of patients with HCC. Patient samples were collected by the Liver Center, Division of Abdominal Transplantation in the Baylor College of Medicine Department of Surgery. Sequencing of HCC is one of the NHGRI Center Initiated Projects in progress in the Human Genome Sequencing Center at Baylor College of Medicine.

Link

dbGap study = phs000509

Palavras-chave

  1. 14/10/2022 14/10/2022 - Chiara Middel
  2. 13/12/2022 13/12/2022 - Kristina Keller
Titular dos direitos

Marie-Claude Gingras, PhD, Baylor College of Medicine, Human Genome Sequencing Center, Houston, TX, USA

Transferido a

13 de dezembro de 2022

DOI

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Licença

Creative Commons BY 4.0

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dbGaP phs000509 Genome Sequencing of Hepatocellular Carcinoma

Eligibility Criteria

Inclusion and exclusion criteria
Descrição

Inclusion and exclusion criteria

All patients with tumors at the time of transplants. Informed consent for participation in genomic research is required.
Descrição

Elig.phs000509.v1.p1.1

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0027651
UMLS CUI [1,2]
C0011008
UMLS CUI [1,3]
C0040732
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C0679823
UMLS CUI [2,3]
C0887950
UMLS CUI [2,4]
C0035168

Similar models

Eligibility Criteria

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
Inclusion and exclusion criteria
Elig.phs000509.v1.p1.1
Item
All patients with tumors at the time of transplants. Informed consent for participation in genomic research is required.
boolean
C0027651 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
C0040732 (UMLS CUI [1,3])
C0021430 (UMLS CUI [2,1])
C0679823 (UMLS CUI [2,2])
C0887950 (UMLS CUI [2,3])
C0035168 (UMLS CUI [2,4])

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