{"database":"EGA","file_versions":[],"scores":null,"additional":{"omics_type":["Genomics"],"study_type":["Whole Genome Sequencing"],"full_dataset_link":["https://ega-archive.org/studies/EGAS00001000417"],"host":["EGA"],"description":["EGA study EGAS00001000417"],"dataset_title":["Genetic studies of pregnancy-related cardiometabolic disorders in Central Asian, Northern European, and Colombian populations (2019-10-29)"],"repository":["EGA"],"category":["restricted"],"name_synonyms":["other disease, Hmong American, Hmong, Caucasians., Asian, familial, disorders, white, Korean American, medical condition, Korean Americans, Pregnancies, Asian unspecified, Cambodian Americans, PREGN, Americans, Filipino American, Caucasian, diseases, European, Japanese, Asian Indian American, Vietnamese Americans, disease or disorder, condition, diseases and disorders, Filipino Americans, Indian American, Asian Americans, Caucasoid, Japanese American, Chinese American, American, human disease, Occidental, Vietnamese American, Gestation, Asian American, Filipino, Cambodian American, Chinese Americans, Asians, genetic, non-neoplastic, Japanese Americans, disease, Cambodian, Korean, Whites, disorder, Homo sapiens disease, White, inherited genetic, constitutitional genetic, Vietnamese, Chinese, Hmong Americans, hereditary, Asian Indian Americans"],"description_synonyms":["Genome-Wide Association, rasGAP, DNS, Hmong American, (Deoxyribonucleotide)n, Hmong, acetylglucosaminyltransferase-like protein, Asian, GAPDH II, Genome Wide Association Analysis, Whole Genome Association Study, 10538, Mbp1, GTPase-activating protein, Gapdh13F, Korean American, GAP1, LARGE1, Deoxyribonucleic acids, froggy, Gyltl1a, Human, Uzbek S.S.R., GADPH, GWA Studies, Filipino American, Deoxyribonucleic Acid, CG8893, gap1, Japanese, Studies, Asian Indian American, Vietnamese Americans, PKWS, Republic of Uzbekistan, Country, myd, FBgn 32821, GWA Study, American, thymus nucleic acid, Kazakh S.S.R., Vietnamese American, like-acetylglucosaminyltransferase, Genomes, RasGAP, MDDGB6, Gapd, GA3PDH, GWA, Kazakh SSR, Gap 1, Filipino, Double Stranded, Mbp-1, mip, Deoxyribonucleic acid, LARGE, GAPDH2, Genome Wide Association Scan, Genome-Wide Association Studies, Asians, genetic, Study, BPFD#36, d-CdGAPr, Cambodian, Gapdh-2, Human Genomes, Korean, CM-AVM, CG6721, Double-Stranded DNA, (Deoxyribonucleotide)m, deoxyribonucleic acids, DNAn, Vietnamese, Chinese, Hmong Americans, constitutitional genetic, Asian Indian Americans, DmelCG8893, WGS, gyltl1b-b, Males, Uzbek SSR, DNAn+1, familial, COUNTRY, Double-Stranded, RASGAP, RASA, Genome-Wide, Korean Americans, Asian unspecified, (Deoxyribonucleotide)n+m, Cambodian Americans, Human Genome., Americans, Genome Wide Association Study, Gapdh, MDDGA6, mKIAA0609, sxt, sequence, Filipino Americans, rare (European definition), Whole Genome Association Analysis, background, rI533, ds-DNA, GAP, Gap, desoxyribose nucleic acid, p120GAP, p120RASGAP, KIAA0609, Indian American, Asian Americans, acetylglucosaminyltransferase-like 1A, Japanese American, GAPDH, Chinese American, fg, Ras-GAP, CG10538, DmelCG6721, gyltl1b, Asian American, DmelCG10538, mdc1d, Cambodian American, whole genome, gap, CMAVM, LARGE_HUMAN, primary structure of sequence macromolecule, Genome Wide Association Studies, Chinese Americans, introduction, Japanese Americans, MDC1D, like-glycosyltransferase, enr, Ras p21 protein activator, ds DNA, Desoxyribonukleinsaeure, Association Studies, inherited genetic, Association Study, DNA, hereditary, Females, glycosyltransferase-like protein LARGE1"],"additional_accession":[]},"is_claimable":false,"name":"Genetic studies of pregnancy related cardiometabolic disorders in Central Asian  Northern European  and Colombian populations","description":"This project aims to generate whole genome sequence (WGS) for 100 unrelated DNA samples from Kazakhstan and 100 unrelated DNA samples from Uzbekistan with the samples in each country equally split between males and females.  The WGS data will be used to impute into much larger Kazakh \nand Uzbek datasets in which genome-wide association studies (GWAS) will be conducted and will also provide more information on rare variants in these Central Asian populations.    In addition, the WGS data will be analysed to determine the genetic and genomic characteristics and peculiarities of these two Central Asian populations to provide background information and infrastructure for future genetic studies in Central Asia and to fill a gap in worldwide information as Central Asia is not currently adequately represented in large genetic resources such as HapMap, 1000Genomes and the Human Genome Diversity panel.","dates":{"updated":"2019-11-04 11:54:03"},"accession":"EGAS00001000417","cross_references":{"TAXONOMY":["9606"],"EGA":["EGAD00001005467","EGAC00001000205"]}}