{"database":"EGA","file_versions":[],"scores":null,"additional":{"omics_type":["Genomics"],"technology_type":["Illumina HiSeq 2000"],"study_type":["Cancer Genomics"],"full_dataset_link":["https://ega-archive.org/studies/EGAS00001000290"],"host":["EGA"],"description":["EGA study EGAS00001000290"],"dataset_title":["Myeloproliferative Disease Whole Genomes"],"repository":["EGA"],"category":["restricted"],"name_synonyms":["non-neoplastic, Core Genome., other disease, disease, human disease, Pan-genome, diseases, Genomes, Diseases, Accessory Genome, disease or disorder, disorders, condition, disorder, diseases and disorders, Homo sapiens disease, medical condition, Pangenome"],"description_synonyms":["Base Pairings, other disease, Disease, human being, DNS, (Deoxyribonucleotide)n, determination, DNAn+1, Modern, Disease Exacerbation, disorders, medical condition, Double-Stranded, Deoxyribonucleic acids, Human, (Deoxyribonucleotide)n+m, Deoxyribonucleic Acid, diseases, Homo sapiens, chemical analysis, Diseases, Clinical Progression, disease or disorder, condition, diseases and disorders, Mutations., ds-DNA, desoxyribose nucleic acid, Library, Man, Progression, Base Pairs, thymus nucleic acid, human disease, Clinical, Man (Taxonomy), Genomes, Double Stranded, Deoxyribonucleic acid, whole genome, human, non-neoplastic, disease, Clinical Course, Base Pair, Modern Man, ds DNA, Exacerbation, Desoxyribonukleinsaeure, disorder, Homo sapiens disease, Double-Stranded DNA, (Deoxyribonucleotide)m, assay, DNA, deoxyribonucleic acids, DNAn, other neoplasm"],"additional_accession":[]},"is_claimable":false,"name":"Myeloproliferative Disease Whole Genomes","description":"Wholegenome libraries will be prepared from at least two serial samples reflecting different stages of disease progression and matched constitutional DNA for 30 Myeloproliferative Disease samples. Five lanes of Illumina HiSeq sequencing will be performed on each of the tumour samples and four lanes for each of the constitutional DNA. Sequencing data will mapped to build 37 of the human reference genome and analysis will be performed to characterize the spectrum of somatic variation present in these samples including single base pair mutations, insertions, deletions as well as larger structural variants and genomic rearrangements.","dates":{"updated":"2017-07-26 15:39:24"},"accession":"EGAS00001000290","cross_references":{"TAXONOMY":["9606"],"EGA":["EGAD00001000385","EGAC00001000010"]}}