EGAGenomicsHiSeq X Ten;ILLUMINAhttps://ega-archive.org/datasets/EGAD000010035102EGA dataset EGAD00001003510EGAVasp, VASP, Data Set., DmelCG15112, ENHANCER OF ATNSI ACTIVITY, MENA, NDPP1, l(2)02029, Enb, enb, ENA, Ena, CG15112, ENA/VASPother disease, BamF, bim, inborn, biml, DNS, HiSeq X Ten, BamC, (Deoxyribonucleotide)n, PreP, DNAn+1, bam, disorders, D10Wsu136e, Genome Sequencing, Cell Lines, connatal, ham, BOD, medical condition, Double-Stranded, Client, Cell, Deoxyribonucleic acids, fs(3)neo61, (Deoxyribonucleotide)n+m, CG10422, MP-1, Complete Genome, Deoxyribonucleic Acid, diseases, Diseases, Line, Pop, disease or disorder, condition, bim-beta7, diseases and disorders, bod, DmelCG10422, ds-DNA, desoxyribose nucleic acid, bimel, Library, Lines, thymus nucleic acid, human disease, Complete, Whole Genome, HCAP, bim-beta6, Complete Genome Sequencing, Ntup1, 2310012C15Rik, Double Stranded, Deoxyribonucleic acid, AI047692, alpha, mKIAA1104, CDLS3, AA410010., BMH, Sequencing, non-neoplastic, disease, BIM, Patient, Bam-C, PrEP, Clients, Whole, BAM, ds DNA, Bam, MP1, Desoxyribonukleinsaeure, SMC3L1, disorder, Homo sapiens disease, Double-Stranded DNA, (Deoxyribonucleotide)m, PE, DNA, deoxyribonucleic acids, DNAn, AI450383, CSPG6, PEPfalseena-DATASET-UMCU-01-08-2017-10:35:35:170-1337 - samplesBAM files with sequencing reads derived from Illumina whole genome sequencing of two DNA samples from lymphoblastoid cell lines from two patients with congenital disease. Whole genome sequencing was performed using Illumina HiSeq X Ten and samples were prepared using TruSeq library prep.2017-08-21 12:50:47EGAD000010035109606EGAC00001000432EGAS00001002333