{"database":"EGA","file_versions":[],"scores":null,"additional":{"omics_type":["Genomics"],"dataset_type":["N/A"],"full_dataset_link":["https://ega-archive.org/datasets/EGAD00001004884"],"sample_count":["47"],"description":["EGA dataset EGAD00001004884"],"repository":["EGA"],"title":["Exome sequencing of synchronous colorectal cancers"],"name_synonyms":["Vasp, VASP, Data Set., DmelCG15112, ENHANCER OF ATNSI ACTIVITY, MENA, NDPP1, l(2)02029, Enb, enb, ENA, Ena, CG15112, ENA/VASP"],"description_synonyms":["Networks, whole exome, Colorectal Neoplasm, Carcinoma, Colorectal Cancer, Family Member, Kinship, Family Research, AW413978, Neoplasms, white, Network, Tumor, Client, Family Members, Colorectal, Caucasian, Abc8, European, Neoplasm, Life Cycle, Colorectal Cancers, HiSeq 4000., Filiation, Caucasoid, Family Life Cycle, Caucasians, Colorectal Tumors, Carcinomas, average, Occidental, Kinship Network, Research, Colorectal Carcinoma, Exomes, Colorectal Carcinomas, patient, Cancers, Colorectal Tumor, Life Cycles, Patient, Whites, Families, Clients, White, Kinship Networks, Family Life Cycles, Family, Relatives, Tumors, Cancer"],"additional_accession":[]},"is_claimable":false,"name":"ena-DATASET-UH-tumorgenomics-02-04-2019-10:42:45:666-263 - samples","description":"The data consists of 47 exome-sequenced synchronous colorectal cancers from 23 patients. The exomes of corresponding normal samples were used to remove germline variants. All patients are Finnish (white Caucasian). All except one patient (sync_11 who belongs to a LS family) were assumed sporadic. The sequence data was produced with Illumina HiSeq 4000.","dates":{"updated":"2019-04-08 08:51:59"},"accession":"EGAD00001004884","cross_references":{"TAXONOMY":["9606"],"EGA":["EGAC00001000987","EGAS00001003474"]}}