This data provider is associated with 101 studies:

Study Accessionsort descending Title
EGAS00001000300 Breast cancer sequential sampling study
EGAS00001000310 RNA sequencing
EGAS00001000374 Deep RNA sequencing in CLL
EGAS00001000389 Whole exome sequencing of virus-associated HCC
EGAS00001000407 Characterization of individual foci of multicentric multifocal breast cancer using targeted next generation sequencing
EGAS00001000549 CPC-GENE Prostate Cancer Heterogeneity Study
EGAS00001000559 ICGC Oesophageal Adenocarcinoma (pilot) - To deeply sequence tumour and normal genomic DNA (including the precursor condition Barretts esophagus when material is available) to provide a comprehensive catalogue of somatic mutations.
EGAS00001000570 Targeted sequencing of genes recurrently mutated in AML part2
EGAS00001000596 Breast Cancer Sequential Sampling Targeted Capture
EGAS00001000671 Whole genome sequencing of Japanese HCCs
EGAS00001000678 WGS of liver cancer in the Japanese population
EGAS00001000704 Metastatic breast cancer targeted gene screen
EGAS00001000706 Whole-Genome sequencing of hepatocellular carcinomas
EGAS00001000723 NORMALS - To deeply sequence tumour and normal genomic DNA (including the precursor condition Barrett’s esophagus when material is available) to provide a comprehensive catalogue of somatic mutations. - This study contains the Normal tissue samples.
EGAS00001000724 100 TUMOURS - To deeply sequence tumour and normal genomic DNA (including the precursor condition Barrett’s esophagus when material is available) to provide a comprehensive catalogue of somatic mutations - This study contains tumour samples from a cohort of 100 patients.

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