{"database":"EGA","file_versions":[],"scores":null,"additional":{"omics_type":["Genomics"],"dataset_type":["Illumina HiSeq 2500;ILLUMINA"],"full_dataset_link":["https://ega-archive.org/datasets/EGAD00001003138"],"sample_count":["54"],"description":["EGA dataset EGAD00001003138"],"repository":["EGA"],"title":["The spatial organization of intratumor heterogeneity and evolutionary trajectories of metastasis in hepatocellular carcinoma"],"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":["WGS, Carcinoma, Liver, Complete Exome Sequencings, Malignant Neoplasm, Data Set, whole blood, Complete Exome, Neoplasms, Exome, Benign Neoplasm, Genome Sequencing, Cell Carcinoma, Liver Cell, adult hepatoma, Tumor, Hepatomas, Malignant, Client, Liver Cell Carcinoma, Cell Carcinomas, Exome Sequencing, Complete Genome, Benign, Client., HCC, Liver Cell Carcinomas, Neoplasm, Adult Liver Cancer, Whole Transcriptome, Transcriptome Sequencing, Adult Liver, Carcinomas, average, WES, Complete Transcriptome, Complete, Complete Transcriptome Sequencing, Exome Sequencings, Whole Genome, Adult Liver Cancers, Hepatocellular carcinoma, Liver Cancer, Malignancy, Hepatoma, Complete Exome Sequencing, Whole Transcriptome Sequencing, Complete Genome Sequencing, adult primary hepatocellular carcinoma, Liver Cancers, Benign Neoplasms, patient, Cancers, Adult, Sequencing, Hepatocellular Carcinoma, Malignant Neoplasms, Neoplasias, Whole Exome, Patient, Clients, Whole, Whole Exome Sequencing, Hepatocellular, Malignancies, Hepatocellular Carcinomas, other neoplasm, Transcriptome Sequencings, Neoplasia, Cancer, Tumors"],"additional_accession":[]},"is_claimable":false,"name":"ena-DATASET-GIS-11-01-2017-10:11:30:626-211 - samples","description":"A dataset consisting of Multi-regional Whole Exome Sequencing (WES) and Whole Genome Sequencing (WGS) data for 54 samples from 9 patients with hepatocellular carcinoma. The dataset includes 45 tumor samples and 9 normal blood samples. Selected somatic variants were validated by Sequenom. Patients covered are: Patient 1, Patient 2, Patient 3, Patient 4, Patient 5, Patient 6, Patient 7, Patient 8, Patient 9 and Patient 10.","dates":{"updated":"2017-07-26 15:39:29"},"accession":"EGAD00001003138","cross_references":{"TAXONOMY":["9606"],"EGA":["EGAC00001000412","EGAS00001001603"]}}