Timo Petteri Sipila, A. Metspalu, P. Happola, P. Palta, M. Kals, A. Palotie
{"title":"北欧外显子组变异目录:基因组数据浏览的网络资源","authors":"Timo Petteri Sipila, A. Metspalu, P. Happola, P. Palta, M. Kals, A. Palotie","doi":"10.1109/eScience.2018.00116","DOIUrl":null,"url":null,"abstract":"Nordic Exome Variant Catalogue is a web tool to browse human genomic aggregation data from Nordic cohorts. This allows viewing, querying, comparison, filtering and sorting the data in graphical user interface. The main end users are researchers and clinicians studying genetic variance in genes of interest.","PeriodicalId":6476,"journal":{"name":"2018 IEEE 14th International Conference on e-Science (e-Science)","volume":"65 1","pages":"393-393"},"PeriodicalIF":0.0000,"publicationDate":"2018-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Nordic Exome Variant Catalogue a Web Resource for Genomic Data Browsing\",\"authors\":\"Timo Petteri Sipila, A. Metspalu, P. Happola, P. Palta, M. Kals, A. Palotie\",\"doi\":\"10.1109/eScience.2018.00116\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Nordic Exome Variant Catalogue is a web tool to browse human genomic aggregation data from Nordic cohorts. This allows viewing, querying, comparison, filtering and sorting the data in graphical user interface. The main end users are researchers and clinicians studying genetic variance in genes of interest.\",\"PeriodicalId\":6476,\"journal\":{\"name\":\"2018 IEEE 14th International Conference on e-Science (e-Science)\",\"volume\":\"65 1\",\"pages\":\"393-393\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2018-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"2018 IEEE 14th International Conference on e-Science (e-Science)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1109/eScience.2018.00116\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"2018 IEEE 14th International Conference on e-Science (e-Science)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/eScience.2018.00116","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Nordic Exome Variant Catalogue a Web Resource for Genomic Data Browsing
Nordic Exome Variant Catalogue is a web tool to browse human genomic aggregation data from Nordic cohorts. This allows viewing, querying, comparison, filtering and sorting the data in graphical user interface. The main end users are researchers and clinicians studying genetic variance in genes of interest.