Whole genome sequencing generated from metastatic gliosarcoma patient samples
This dataset contains whole genome sequencing data aligned to the b37 reference genome for 4 spatially and temporally distinct tumors from one patient with a matched normal blood sample.
- 5 samples
- DAC: EGAC00001001434
- Technologies: HiSeq X Ten, Illumina NovaSeq 6000
Access to sequencing data is available by application to the Metastatic Gliosarcoma Case Study DAC. Access to data will be granted to qualified investigators for appropriate use.
Access to the data requires that you agree to the following terms and conditions: (1) Not relate other individually-identifiable data to which you have access, e.g., privately held datasets from your institution, to this patient's data, for any purpose, and not otherwise generate information that could allow this patient's identity to be ascertained (2) Not commercialize any product that contains data from this resource (3) Provide appropriate acknowledgement to this study in any dissemination, presentation, or other publication of research findings using this data resource (4) Report to the DAC any inadvertent data release, breach of data security, or other data management incidents that are inconsistent with these terms of use
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 |
|---|---|---|
| EGAS00001004076 | Other |