ID

45509

Description

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.

Lien

dbGap study = phs000509

Mots-clés

  1. 14/10/2022 14/10/2022 - Chiara Middel
  2. 13/12/2022 13/12/2022 - Kristina Keller
Détendeur de droits

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

Téléchargé le

13 décembre 2022

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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dbGaP phs000509 Genome Sequencing of Hepatocellular Carcinoma

Eligibility Criteria

Inclusion and exclusion criteria
Description

Inclusion and exclusion criteria

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

Elig.phs000509.v1.p1.1

Type de données

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
Type
Description | Question | Decode (Coded Value)
Type de données
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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