{"database":"ENA","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Fastqsanger.gz":["ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR198/000/SRR1982880/SRR1982880.fastq.gz","ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR198/009/SRR1982879/SRR1982879.fastq.gz","ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR198/003/SRR1982583/SRR1982583.fastq.gz"]},"type":"primary"},"statusCodeValue":200,"statusCode":"OK"}],"scores":null,"additional":{"omics_type":["Genomics"],"center_name":["Brigham and Women's Hospital"],"full_dataset_link":["https://www.ebi.ac.uk/ena/browser/view/PRJNA281714"],"scientific_name":["Homo sapiens"],"tag":["xref:EuropePMC:PMC4551903"],"long_description":["Gene-trap virus was produced in 293T cells by transfection of gene-trap vectors combined with pAdvantage, CMV-VSVG and Gag-pol. Approximately 100 million near haploid KBM-7 cells were infected and subsequently expanded. Cells were exposed to MG132 or Velcade and resistant clones were expanded and pooled. From the pooled clones genomic DNA was isolated and used to map insertion sites using inverse PCR. Mutations that were predicted to be disruptive in genes were counted per gene and compared to mutation frequencies in the same gene in a non-selected contra, cell population. Genes significantly enriched for mutations in the selected cell population were identified."],"repository":["ENA"],"description_synonyms":["Human, Complete., human being, Complete Genome, Whole Genome, Man (Taxonomy), Homo sapiens, Modern Man, Whole, Modern, Complete Genome Sequencing, Genome Sequencing, man, Man, human, Sequencing"],"name_synonyms":["Human, Modern., human being, Man (Taxonomy), Homo sapiens, man, Man, human, Modern Man"],"additional_accession":[]},"is_claimable":false,"name":"Homo sapiens","description":"Homo sapiens KBM-7 Whole genome sequencing","dates":{"last_updated":"2025-09-24","first_public":"2015-04-23"},"accession":"PRJNA281714","cross_references":{"taxon":["9606"]}}