ID
45616
Description
Principal Investigator: Hanlee Ji, MD, Stanford University School of Medicine, Stanford, CA, USA MeSH: Stomach Neoplasms,Krukenberg Tumor https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs001362 In this study, linked read sequencing was performed on two ovarian metastases and matched normal tissue, from a patient with primary diffuse gastric cancer. Linked read sequencing is a DNA preparation technology whereby high molecular weight molecules of DNA are uniquely barcoded prior to fragmentation and sequencing, thus retaining information about genomic contiguity. This study performed an extended analysis of linked read sequencing data to resolve the complex structures of structural variants in the cancer genomes. Complex structural rearrangements were identified in the genomic region surrounding the known oncogene FGFR2, and the association between FGFR2 and gastric cancer metastasis was demonstrated in an organoid model.
Lien
Mots-clés
Versions (1)
- 26/02/2023 26/02/2023 - Simon Heim
Détendeur de droits
Hanlee Ji, MD, Stanford University School of Medicine, Stanford, CA, USA
Téléchargé le
26 février 2023
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY 4.0
Modèle Commentaires :
Ici, vous pouvez faire des commentaires sur le modèle. À partir des bulles de texte, vous pouvez laisser des commentaires spécifiques sur les groupes Item et les Item.
Groupe Item commentaires pour :
Item commentaires pour :
Vous devez être connecté pour pouvoir télécharger des formulaires. Veuillez vous connecter ou s’inscrire gratuitement.
dbGaP phs001362 Linked Read Sequencing of Gastric Cancer Metastases
This subject phenotype table contains subject ID, sex, age of onset, and race.
- StudyEvent: SEV1
- The subject consent file includes subject IDs, consent information, and affection status of the subject for gastric cancer.
- This data table contains a mapping of study subject IDs to sample IDs. Samples are the final preps submitted for genotyping, sequencing, and/or expression data. For example, if one patient (subject ID) gave one sample, and that sample was processed differently to generate 2 sequencing runs, there would be two rows, both using the same subject ID, but having 2 unique sample IDs. The data table also includes sample use.
- This subject phenotype table contains subject ID, sex, age of onset, and race.
- This sample attributes table contains sample ID, body site where tumor sample was collected, analyte type, tumor status, histological type, and primary tumor or metastasis.
Similar models
This subject phenotype table contains subject ID, sex, age of onset, and race.
- StudyEvent: SEV1
- The subject consent file includes subject IDs, consent information, and affection status of the subject for gastric cancer.
- This data table contains a mapping of study subject IDs to sample IDs. Samples are the final preps submitted for genotyping, sequencing, and/or expression data. For example, if one patient (subject ID) gave one sample, and that sample was processed differently to generate 2 sequencing runs, there would be two rows, both using the same subject ID, but having 2 unique sample IDs. The data table also includes sample use.
- This subject phenotype table contains subject ID, sex, age of onset, and race.
- This sample attributes table contains sample ID, body site where tumor sample was collected, analyte type, tumor status, histological type, and primary tumor or metastasis.
C2348585 (UMLS CUI [1,2])