EGAC00001000000

EGAC00001000000

DAC Accession Contact Person Email Access Information
EGAC00001000000 Data Sharing datasharing@sanger.ac.uk http://www.ebi.ac.uk/ega/dacs/EGAC00001000000

This DAC controls 242 datasets:

Dataset Accessionsort descending Technology Samples Description
EGAD00000000051 Illumina Genome Analyzer II 25 Sequencing data from matching Renal Carcinoma samples
EGAD00000000052 Illumina Genome Analyzer II 25 Sequencing data from natching Pancreatic Carcinoma samples
EGAD00000000053 Illumina Genome Analyzer II 1 Sequencing data from Breast Cancer samples
EGAD00000000054 Life Tech - Solid 1 NCI-H209 is an immortal cell line derived from a bone marrow metastasis of a patient with small cell lung cancer, taken before chemotherapy. The specimen showed histologically typical small cells with classic neuroendocrine features. NCI-BL209 is an EBV-transformed B-cell line derived from the same patient as the small cell lung cancer cell line, NCI-H209
EGAD00000000055 Illumina Genome Analyzer II 2 COLO-829 is a publicly available immortal cancer cell line and COLO-829BL is a lymphoblastoid cell line derived from the same patient
EGAD00001000001 18 Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma
EGAD00001000002 11 Massive genomic rearrangement acquired in a single catastrophic event during cancer development
EGAD00001000004 Illumina Genome Analyzer II, Illumina Genome Analyzer 5 CLL cancer Sample Sequencing
EGAD00001000005 Illumina Genome Analyzer II;, Illumina Genome Analyzer II 14 Various Cancer Fusion Gene Sequencing
EGAD00001000007 Illumina Genome Analyzer II;, Illumina Genome Analyzer II 43 Osteosarcoma Sequencing
EGAD00001000013 Illumina Genome Analyzer II 19 CLL Cancer Whole Genome Sequencing
EGAD00001000014 Illumina Genome Analyzer II;, Illumina Genome Analyzer II 54 Agilent whole exome hybridisation capture will be performed on genomic DNA derived from 25 renal cancers and matched normal DNA from the same patients. Three lanes of Illumina GA sequencing will be performed on the resulting 50 exome libraries and mapped to build 37 of the human reference genome to facilitate the identification of novel cancer genes.
EGAD00001000050 Illumina Genome Analyzer II 13 Tandem duplication of chromosomal segments is common in ovarian and breast cancer genomes
EGAD00001000062 Illumina HiSeq 2000, Illumina Genome Analyzer II 14 ADCC Rearrangement Screen
EGAD00001000064 Illumina Genome Analyzer II 6 Cell Line Sub Clone Rearrangement Screen

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