CLL cancer Sample Sequencing

Study ID Alternative Stable ID Type
EGAS00001000011 Cancer Genomics

Study Description

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.

Study Datasets 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
Massive genomic rearrangement acquired in a single catastrophic event during cancer development
Illumina Genome Analyzer,Illumina Genome Analyzer II 11
CLL cancer Sample Sequencing
Illumina Genome Analyzer,Illumina Genome Analyzer II 5
Whole genome sequencing of single cell derived organoids from normal colon tissue and colorectal cancer.
HiSeq X Ten 73

Who archives the data?

There are no publications available