{"database":"EGA","file_versions":[],"scores":null,"additional":{"omics_type":["Genomics"],"study_type":["Synthetic Genomics"],"full_dataset_link":["https://ega-archive.org/studies/EGAS00001000009"],"host":["EGA"],"description":["EGA study EGAS00001000009"],"dataset_title":["Massive genomic rearrangement acquired in a single catastrophic event during cancer development"],"repository":["EGA"],"category":["restricted"],"name_synonyms":["small cell cancer of the lung, SCLC1."],"description_synonyms":["CXXC9, DNA (cytosine-5)-methyltransferase 1, DNMT1, study, ADCADN, UNQ203/PRO229, CT-2, Edg, HSN1E, DNMT1_HUMAN, DNA (cytosine-5-)-methyltransferase 1, DNMT, MCMT, CXXC-type zinc finger protein 9, API6, Aim, AIM, HHT1., DNA methyltransferase HsaI, ORW1, CXXC finger protein 9, END, CLEC2C, m.HsaI, DNA MTase HsaI"],"additional_accession":[]},"is_claimable":false,"name":"SCLC","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).","dates":{"updated":"2024-10-02 14:22:39"},"accession":"EGAS00001000009","cross_references":{"TAXONOMY":["9606"],"EGA":["EGAD00001000002","EGAC00001000000"]}}