Study ID Alternative Stable ID Type
EGAS00001000009 Synthetic Genomics

Study Description

The aim of this study is to use sequence data generated from 500 bp paired end reads using the Illumina platform to characterise the breakpoints of chromosomal translocations, amplifications and deletions at high resolution (to the bp).

Study Datasets 1 dataset.

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

Who archives the data?

There are no publications available