{"database":"EGA","file_versions":[],"scores":null,"additional":{"omics_type":["Genomics"],"technology_type":["Illumina HiSeq 2500, ILLUMINA"],"study_type":["Whole Genome Sequencing"],"full_dataset_link":["https://ega-archive.org/studies/EGAS00001002084"],"host":["EGA"],"description":["EGA study EGAS00001002084"],"dataset_title":["WGS data from Lebanon"],"repository":["EGA"],"category":["restricted"],"name_synonyms":["Lebanese Republic."],"description_synonyms":["INAD1, Forms, PRE, Hunter Carpenter Macdonald syndrome, KARAK syndrome, Genomics, cou, early onset of peripheral gangrene, PhrB photolyase activity, neuroaxonal dystrophy, PLAN, Comparative, deoxyribonucleic cyclobutane dipyrimidine photolyase activity, PLA2G6 neurodegeneration with brain iron accumulation, Functional Genomics, photoreactivating enzyme activity, Tl3, pigmented epithelium, Tl2, Pangenome, Publication., School-Age, infantile, MODIFIER OF SNC1, infantile neuroaxonal dystrophy/atypical neuroaxonal dystrophy, Lr, Structural, neurodegeneration with brain iron accumulation caused by mutation in PLA2G6, retinal pigment, Publication, INAD, School Age, Core Genome, deoxyribonucleic photolyase activity, Functional, sequence, dipyrimidine photolyase (photosensitive), 3, Hunter-Carpenter-McDonald syndrome, stratum pigmentosa retinae, Low, NUP96, epithelium, retinal pigment layer, School-Age Populations, Populations, me75, MOS3, RPE, deoxyribocyclobutadipyrimidine pyrimidine-lyase activity, Seitelberger disease, neuroaxonal dystrophy presenting with neonatal dysmorphic features, Genomes, PRECOCIOUS, photolyase activity, Comparative Genomics, Accessory Genome, pigmented retina, F23A5.3, whole genome, Population, School Age Populations, D17Mit170, sample population, included, primary structure of sequence macromolecule, T1, DNA cyclobutane dipyrimidine photolyase activity, SUPPRESSOR OF AUXIN RESISTANCE 3, p. pigmentosa retinae, phr A photolyase activity, Pan-genome, DNA-photoreactivating enzyme, sample, Bra, Structural Genomics, deoxyribonucleate pyrimidine dimer lyase (photosensitive), School-Age Population, Phospholipase A2-associated neurodegeneration, School Age Population, African unspecified, F23A5_3"],"additional_accession":[]},"is_claimable":false,"name":"Lebanon LowCov seq","description":"we propose to investigate the genomics of a Lebanese sample. we plan (1) genotyping (2.5M) of 120 Lebanese individuals, choosing this platform to allow comparison with the 1000 Genomes and African Genome Variation project populations, (2) 8x sequencing of 100 individuals to provide unbiased population-level sequence information including allele frequencies, and (3) 30x sequencing of four individuals to allow inferences such as from PSMC/MSMC to be obtained. The current form is for the low-coverage sequencing.  \nThis data is part of a pre-publication release. For information on the proper use of pre-publication data shared by the Wellcome Trust Sanger Institute (including details of any publication moratoria), please see http://www.sanger.ac.uk/datasharing/","dates":{"updated":"2017-07-26 15:39:29"},"accession":"EGAS00001002084","cross_references":{"TAXONOMY":["9606"],"EGA":["EGAD00001003098","EGAC00001000205"]}}