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{"accession_id":"EGAD00001006902","title":"WGS fastq for EGAS00001004572","description":"Bulk WGS fastq files for germline and tumours in EGAS00001004572.","dataset_types":["Whole genome sequencing"],"technologies":["HiSeq X Ten","Illumina HiSeq X"],"num_samples":1,"access_type":"controlled","is_in_beacon":false,"is_released":true,"released_date":"2021-01-25T22:04:45+01:00","is_deprecated":false,"policy_accession_id":"EGAP00001001849"},
{"accession_id":"EGAD00001006906","title":"GRIDSS somatic sv vcfs for EGAS00001004572","description":"Bulk GRIDSS somatic sv vcfs from tumour-normal analysis in EGAS00001004572","dataset_types":["Genomic variant calling"],"technologies":null,"num_samples":1,"access_type":"controlled","is_in_beacon":false,"is_released":true,"released_date":"2021-01-26T22:54:24+01:00","is_deprecated":false,"policy_accession_id":"EGAP00001001849"},
{"accession_id":"EGAD00001006907","title":"Strelka somatic snv vcfs for EGAS00001004572","description":"Bulk Strelka somatic snv vcfs from tumour-normal analysis in EGAS00001004572","dataset_types":["Genomic variant calling"],"technologies":null,"num_samples":1,"access_type":"controlled","is_in_beacon":false,"is_released":true,"released_date":"2021-01-27T01:36:24+01:00","is_deprecated":false,"policy_accession_id":"EGAP00001001849"},
{"accession_id":"EGAD00001006908","title":"Purple copy number segments for EGAS00001004572","description":"Bulk copy number segments from Purple analysis in EGAS00001004572","dataset_types":["Phenotype information"],"technologies":null,"num_samples":1,"access_type":"controlled","is_in_beacon":false,"is_released":true,"released_date":"2021-01-27T02:09:39+01:00","is_deprecated":false,"policy_accession_id":"EGAP00001001849"},
{"accession_id":"EGAD00001006909","title":"Methylation tumour profiles for EGAS00001004572","description":"Bulk methylation tumour profiles from infinium methylation epic bead kit in EGAS00001004572","dataset_types":["Methylation profiling by high-throughput sequencing"],"technologies":null,"num_samples":1,"access_type":"controlled","is_in_beacon":false,"is_released":true,"released_date":"2021-01-27T04:59:56+01:00","is_deprecated":false,"policy_accession_id":"EGAP00001001849"},
{"accession_id":"EGAD00001006910","title":"Germline snv g.vcf for EGAS00001004572","description":"Bulk Germline snv vcfs from haplotypecaller analysis in EGAS00001004572","dataset_types":["Genomic variant calling"],"technologies":null,"num_samples":1,"access_type":"controlled","is_in_beacon":false,"is_released":true,"released_date":"2021-01-27T05:08:42+01:00","is_deprecated":false,"policy_accession_id":"EGAP00001001849"},
{"accession_id":"EGAD00001008358","title":"Target pilot trial","description":"In vitro and in vivo drug screens of tumor cells identify novel therapies for high-risk child cancer","dataset_types":["Genomic variant calling","Transcriptome profiling by high-throughput sequencing","Whole genome sequencing"],"technologies":["HiSeq X Ten","NextSeq 500"],"num_samples":1,"access_type":"controlled","is_in_beacon":false,"is_released":true,"released_date":"2021-11-22T03:49:24+01:00","is_deprecated":false,"policy_accession_id":"EGAP00001001849"},
{"accession_id":"EGAD00001015625","title":"consHLA extra samples for comparison with clinical HLA types","description":"Samples not in other datasets for the paper titled;\nconsHLA: a Next Generation Sequencing Consensus-based HLA Typing Workflow","dataset_types":["Whole genome sequencing"],"technologies":["Illumina NovaSeq 6000"],"num_samples":8,"access_type":"controlled","is_in_beacon":false,"is_released":true,"released_date":"2025-06-20T07:27:26+02:00","is_deprecated":false,"policy_accession_id":"EGAP00001001849"}]