CLL_cancer_Sample_Sequencing

Genomic libraries (500 bps) will be generated from total genomic DNA derived from CLL cancer samples and subjected to total of eight lanes of 37 bp, paired end sequencing on the llumina GA. Paired reads will be mapped to build 37 of the human reference genome to facilitate the generation of genome wide copy number information, and the identification of novel rearranged cancer genes and gene fusions.

Type: Cancer Genomics
Archiver: European Genome-Phenome Archive (EGA)

3 Datasets

Click on a Dataset ID in the table below to learn more, and to find out who to contact about access to these data

Dataset ID	Description	Technology	Samples
EGAD00001000002	Massive genomic rearrangement acquired in a single catastrophic event during cancer development	Illumina Genome Analyzer Illumina Genome Analyzer II	1
EGAD00001000004	CLL cancer Sample Sequencing	Illumina Genome Analyzer Illumina Genome Analyzer II	5
EGAD00001001447	Whole genome sequencing of single cell derived organoids from normal colon tissue and colorectal cancer.	HiSeq X Ten	19