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Massive genomic rearrangement acquired in a single catastrophic event during cancer development
Cancer is driven by mutation. Using Agilent exome hybridisation capture and Illumina GA massively parallel sequencing technology, we aim to sequence ~1600 microRNAs plus the protein coding genome of 25 matched human renal cancer samples. Bespoke algorithms are being developed to identify the somatic...
A dataset of ~600 RIL crosses using RILs from the Drosophila Synthetic Population Resource to be used for genomewide eQTL mapping. All samples are from female heads. 54 arrays with 12 samples per array resulting in data for 596 RIL crosses.
ORGANISM(S): Drosophila melanogaster 
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