{"database":"EGA","file_versions":[],"scores":null,"additional":{"omics_type":["Genomics"],"technology_type":["Illumina HiSeq 2000"],"study_type":["Cancer Genomics"],"full_dataset_link":["https://ega-archive.org/studies/EGAS00001000434"],"host":["EGA"],"description":["EGA study EGAS00001000434"],"dataset_title":["Somatic pseudogenes acquired during cancer development – RNAseq","Matched Pair Cell Line Tumour RNAseq"],"category":["restricted"],"repository":["EGA"],"name_synonyms":["Line, Cell Lines, Cell, other neoplasm., Lines"],"description_synonyms":["study, whole exome, Complete, Transcriptome, Whole Genome, Transcriptome Profile, Profile, Expression Profiles, Complete Genome Sequencing, Genome Sequencing, Gene Expression Profile, Gene, Profiles, Signatures, primary structure of sequence macromolecule, Sequencing, Gene Expression, Complete Genome, Expression Signature, Gene Expression Profiles, Expression Signatures, Whole, Gene Expression Signatures, Transcriptomes, sequence, Mutations., Gene Expression Signature, Signature, other neoplasm, Expression Profile, Catalogs, Transcriptome Profiles"],"additional_accession":[]},"is_claimable":false,"name":"Matched Pair Cell Line Tumour RNAseq","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.","dates":{"updated":"2020-07-16 15:39:02"},"accession":"EGAS00001000434","cross_references":{"TAXONOMY":["9606"],"EGA":["EGAD00001000639","EGAD00001000630","EGAC00001000000"]}}