{"data":{"id":"10.25387/g3.6713156","type":"dois","attributes":{"doi":"10.25387/g3.6713156","prefix":"10.25387","suffix":"g3.6713156","identifiers":[{"identifier":"https://doi.org/10.25387/g3.6713156","identifierType":"DOI"}],"alternateIdentifiers":[{"alternateIdentifierType":"DOI","alternateIdentifier":"https://doi.org/10.25387/g3.6713156"}],"creators":[{"name":"Jiun-Sheng Chen","affiliation":[],"nameIdentifiers":[]},{"name":"Fulan Hu","affiliation":[],"nameIdentifiers":[]},{"name":"Subra Kugathasan","affiliation":[],"nameIdentifiers":[]},{"name":"Jorde, Lynn B.","nameType":"Personal","givenName":"Lynn B.","familyName":"Jorde","affiliation":[],"nameIdentifiers":[]},{"name":"Nix, David","nameType":"Personal","givenName":"David","familyName":"Nix","affiliation":[],"nameIdentifiers":[]},{"name":"Rutherford, Ann","nameType":"Personal","givenName":"Ann","familyName":"Rutherford","affiliation":[],"nameIdentifiers":[]},{"name":"Denson, Lee","nameType":"Personal","givenName":"Lee","familyName":"Denson","affiliation":[],"nameIdentifiers":[]},{"name":"W. Scott Watkins","affiliation":[],"nameIdentifiers":[]},{"name":"Sampath Prahalad","affiliation":[],"nameIdentifiers":[]},{"name":"Huff, Chad","nameType":"Personal","givenName":"Chad","familyName":"Huff","affiliation":[],"nameIdentifiers":[]},{"name":"Guthery, Stephen L.","nameType":"Personal","givenName":"Stephen L.","familyName":"Guthery","affiliation":[],"nameIdentifiers":[]}],"titles":[{"title":"Supplemental Material for Chen et al., 2018"}],"publisher":"Figshare","container":{},"publicationYear":2018,"subjects":[{"subject":"110311 Medical Genetics (excl. Cancer Genetics)","subjectScheme":"FOR"},{"subject":"FOS: Basic medicine","schemeUri":"http://www.oecd.org/science/inno/38235147.pdf","subjectScheme":"Fields of Science and Technology (FOS)"},{"subject":"60102 Bioinformatics","subjectScheme":"FOR"},{"subject":"FOS: Computer and information sciences","schemeUri":"http://www.oecd.org/science/inno/38235147.pdf","subjectScheme":"Fields of Science and Technology (FOS)"}],"contributors":[],"dates":[{"date":"2018-06-28","dateType":"Created"},{"date":"2018-06-28","dateType":"Updated"},{"date":"2018","dateType":"Issued"}],"language":null,"types":{"ris":"GEN","bibtex":"misc","citeproc":"article","schemaOrg":"Collection","resourceType":"Fileset","resourceTypeGeneral":"Collection"},"relatedIdentifiers":[{"relationType":"IsSupplementTo","relatedIdentifier":"10.1534/g3.118.200404","relatedIdentifierType":"DOI"}],"relatedItems":[],"sizes":["307388 Bytes"],"formats":[],"version":null,"rightsList":[{"rights":"CC BY 4.0","rightsUri":"https://creativecommons.org/licenses/by/4.0"}],"descriptions":[{"description":"Table S1 lists 101 targeted genes.Table S2 lists 63 testable genes for multiple test correction.Table S3 shows VAAST results for genes with p-value less than 0.05.Tables S4, S5 and S6 contain the resources and data used for meta-analyses.Figure S1 contains clinical characteristics of cases.Figure S2 shows a PCA plot of cases and controls superimposed on HapMap 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