<HashMap><database>EGA</database><scores/><additional><omics_type>Genomics</omics_type><dataset_type>N/A</dataset_type><full_dataset_link>https://ega-archive.org/datasets/EGAD00001004319</full_dataset_link><sample_count>30</sample_count><description>EGA dataset EGAD00001004319</description><repository>EGA</repository><title>Resolving the Full Spectrum of Human Genome Variation using Linked-Reads</title><name_synonyms>Vasp, VASP, DmelCG15112, ENHANCER OF ATNSI ACTIVITY, Data Set, MENA, NDPP1, l(2)02029, Enb, enb, ENA, Ena, CG15112, 2018., ENA/VASP</name_synonyms><description_synonyms>other disease, Bru, BamF, bim, biml, Raw, experimental, BamC, determination, Complete Exome, bam, VCFS, fs(3)neo61, CG10422, diseases, CTHM, DGCR, DORV, TGA, disease or disorder, DGS, diseases and disorders, bim-beta7, Whole Transcriptome, Transcriptome Sequencing, Del(8)44H, DmelCG10422, VCF, Svc, WES, human disease, Complete, methods, Exome Sequencings, HCAP, bim-beta6, experimental section, Complete Exome Sequencing, Whole Transcriptome Sequencing, Tissue, CDLS3, BMH, Sequencing, Transplant Donors, non-neoplastic, Whole Exome, Whole, sample, disorder, Homo sapiens disease, Tissue Donor, Ovum Donor, CSPG6, Organ, Data Set., Transplant Donor, Complete Exome Sequencings, Data Set, Transplant, Exome, disorders, Semen Donors, ham, BOD, medical condition, read, Exome Sequencing, chemical analysis, Diseases, condition, Donor, Donors, CAFS, bod, bimel, Complete Transcriptome, Complete Transcriptome Sequencing, Col4a-1, Organ Donor, alpha, sample population, Semen Donor, experimental procedures, disease, TBX1C, Semen, BIM, Bam-C, BAM, Whole Exome Sequencing, Bam, CATCH22, SMC3L1, assay, Transcriptome Sequencings, Ovum, Ovum Donors, Organ Donors</description_synonyms></additional><is_claimable>false</is_claimable><name>ena-DATASET-10xGenomics-31-08-2018-17:01:50:525-55 - samples</name><description>This dataset contains Linked-Read Whole Exome Sequencing (lrWES) from individuals with known disease-causing variants. The dataset comprises of 30 samples from 10 donors, where multiple samples from the same donor reflect experimental differences assaying the effect of input DNA length on coverage and phasing. Raw data (i.e. BAM files) and variant analysis (i.e. VCF files) for each sample are included in this dataset.</description><dates><updated>2018-10-23 09:51:02</updated></dates><accession>EGAD00001004319</accession><cross_references><TAXONOMY>9606</TAXONOMY><EGA>EGAC00001000996</EGA><EGA>EGAS00001003121</EGA></cross_references></HashMap>