[{"accession_id":"EGAD00001010928","title":"Whole exome sequencing of tumors from the Precision Medicine Program in Pediatric and Adolescent Patients with Recurrent Malignancies","description":"Sequencing libraries were constructed according to standard procedures from 600 ng\nof tumor and paired constitutional DNA. WES was captured using Agilent SureSelect V5 (50\nMb), Clinical Research Exome (54 Mb) kit, SureSelect XT human All exon CRE version 1 or\n2, or Twist Human Core Exome Enrichment System. Sequencing of subsequent libraries was\nperformed using Illumina sequencers (Next-Seq 500 or Hiseq 2000/2500/4000) in 75 bp\npaired-end mode, aiming for a mean depth of coverage of 100x.","dataset_types":["Exome sequencing","Genomic variant calling"],"technologies":["Illumina HiSeq 4000"],"num_samples":1376,"access_type":"controlled","is_in_beacon":false,"is_released":true,"released_date":"2023-06-05T14:42:32+02:00","is_deprecated":false,"policy_accession_id":"EGAP00001003339"}]