NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE270257 Query DataSets for GSE270257
Status Public on Oct 15, 2024
Title Long-Read Sequencing of an Advanced Cancer Cohort Resolves Rearrangements, Unravels Haplotypes, and Reveals Methylation Landscapes
Organism Homo sapiens
Experiment type Methylation profiling by high throughput sequencing
Summary The Long-read POG dataset comprises a cohort of 189 patient tumours and 41 matched normal samples sequenced using the Oxford Nanopore Technologies PromethION platform. This dataset from the Personalized Oncogenomics (POG) program and the Marathon of Hope Cancer Centres Network includes accompanying DNA and RNA short-read sequence data, analytics, and clinical information. We show the potential of long-read sequencing for resolving complex cancer-related structural variants, viral integrations, and extrachromosomal circular DNA. Long-range phasing of variants facilitates the discovery of allelically differentially methylated regions (aDMRs) and allele-specific expression, including recurrent aDMRs in the cancer genes RET and CDKN2A. Germline promoter methylation in MLH1 can be directly observed in Lynch syndrome. Promoter methylation in BRCA1 and RAD51C is a likely driver behind patterns of homologous recombination deficiency where no driver mutation was found. This dataset demonstrates applications for long-read sequencing in precision medicine, and is available as a resource for developing analytical approaches using this technology.
 
Overall design We sequenced 189 patient tumours and 41 matched normal (blood) samples. We show the potential of long-read sequencing for resolving complex cancer-related structural variants, viral integrations, and extrachromosomal circular DNA by sequencing . Long-range phasing of variants facilitates the discovery of allelically differentially methylated regions (aDMRs) and allele-specific expression. Associated WGS data are available at the European Genome-phenome Archive (EGA) under study accession number: EGAS00001001159. Additional open data and code is available at https://github.com/bcgsc/long_read_pog

***************************************************************
Raw data are available at the European Genome-phenome Archive (EGA) under study accession number: EGAS00001001159.
***************************************************************
 
Citation(s) 39406235
Submission date Jun 19, 2024
Last update date Oct 16, 2024
Contact name Marco Marra
E-mail(s) [email protected]
Organization name Canada's Michael Smith Genome Sciences Centre
Street address 570 W 7th Ave
City Vancouver
State/province BC
ZIP/Postal code V5Z 4S6
Country Canada
 
Platforms (1)
GPL26167 PromethION (Homo sapiens)
Samples (232)
GSM8338252 D36494
GSM8338253 D36497
GSM8338254 D36500
Relations
BioProject PRJNA1125915

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE270257_RAW.tar 2.7 Tb (http)(custom) TAR (of TSV)
Raw data not provided for this record

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap