Study ID Alternative Stable ID Type
EGAS00001000148 Cancer Genomics

Study Description

We propose to definitively characterise the somatic genetics of Lung cancer through generation of comprehensive catalogues of somatic mutations by high coverage genome sequencing.

Study Datasets 2 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
Lung Cancer Whole Genomes
Illumina HiSeq 2000 18
Insertion of processed pseudogenes is known to occur in the germline but has not previously been observed in somatic cells. Formation of pseudogenes could represent a new class of mutation in cancers and a new source of potential driver events.
Illumina HiSeq 2000 20

Who archives the data?

There are no publications available