Matched_Pair_Cell_Line_Tumour_RNAseq - EGA European Genome-Phenome Archive

Study

Matched Pair Cell Line Tumour RNAseq

Study ID	Alternative Stable ID	Type
EGAS00001000434		Cancer Genomics

Study Description

In this study we will sequence the transcriptome of Verified Matched Pair Cancer Cell line tumour samples. This will be married up to whole exome and whole genome sequencing data to establish a full catalog of the variations and mutations found.

Study Datasets 2 datasets.

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Dataset ID	Description	Technology	Samples
EGAD00001000630	In this study we will sequence the transcriptome of Verified Matched Pair Cancer Cell line tumour samples. This will be married up to whole exome and whole genome sequencing data to establish a full catalog of the variations and mutations found. In this study we will sequence the transcriptome of Verified Matched Pair Cancer Cell line tumour samples. This will be married up to whole exome and whole genome sequencing data to establish a full catalog of the variations and mutations found.	Illumina HiSeq 2000	7
EGAD00001000639	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. 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	3

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