Haplotype-specific assembly of shattered chromosomes in oesophageal adenocarciomas
Genomic and epigenomic sequencing of 5 oesphageal adenocarciomas with evidence of chromothripsis. Genomic sequencing includes: Pacbio circular consensus sequencing, Pacbio continuous long read sequencing, 10X linked read and Illumia HiSeq X Ten sequencing. Epigenomic sequencing includes: Hi-C chromosome capture, ATAC-seq, ChIP seq (for H3K27ac, H3K4me3, H3K27me3 and CTCF) and long read RNA sequencing. All data types have the bam files which have not undergone haplotype resolution (demarcated as unresolved) and some data types also have haplotype resolved reads (demarcated as resolved).
- DAC: EGAC00001000000
DUO:0000019 version: 2021-02-23
publication required
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DUO:0000026 version: 2021-02-23
user specific restriction
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DUO:0000028 version: 2021-02-23
institution specific restriction
This data use modifier indicates that use is limited to use within an approved institution.
DUO:0000042 version: 2021-02-23
general research use
This data use permission indicates that use is allowed for general research use for any research purpose.
Wellcome Trust Sanger Institute Cancer Genome Group Data Sharing Policy
Studies are experimental investigations of a particular phenomenon, e.g., case-control studies on a particular trait or cancer research projects reporting matching cancer normal genomes from patients.
| Study ID | Study Title | Study Type |
|---|---|---|
| EGAS00001003122 | Cancer Genomics | |
| EGAS00001003191 | Cancer Genomics | |
| EGAS00001003264 | Cancer Genomics | |
| EGAS00001003890 | Cancer Genomics | |
| EGAS00001004051 | Cancer Genomics | |
| EGAS00001007163 | Cancer Genomics | |
| EGAS00001007180 | Cancer Genomics |