{"title":"问题信息","authors":"","doi":"10.1002/cphg.91","DOIUrl":null,"url":null,"abstract":"<p><b>Cover</b>: In Spector and Wiita. (http://doi.org/10.1002/cphg.106), the image shows a screenshot of ClinTAD's <b><i>Single</i></b> page for the example case. The top section of this page contains the input fields. The middle section contains an interactive visualization with several types of elements. These elements can include topologically associated domains (red), the copy number variant (green), genes with no phenotype matches (blue), genes with phenotype matches (orange), VISTA enhancers (purple), and DGV duplications (blue) and deletions (red). For the example case, both the <i>MCTP2</i> (left side) and <i>NR2F2</i> (right side) genes are highlighted in orange, indicating that they are associated with phenotypes that match to the patient. The last section of the page shows additional information for elements that are clicked on, in this case the <i>MCTP2</i> gene.\n\n <figure>\n <div><picture>\n <source></source></picture><p></p>\n </div>\n </figure></p>","PeriodicalId":40007,"journal":{"name":"Current Protocols in Human Genetics","volume":"108 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cphg.91","citationCount":"0","resultStr":"{\"title\":\"Issue Information\",\"authors\":\"\",\"doi\":\"10.1002/cphg.91\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><b>Cover</b>: In Spector and Wiita. (http://doi.org/10.1002/cphg.106), the image shows a screenshot of ClinTAD's <b><i>Single</i></b> page for the example case. The top section of this page contains the input fields. The middle section contains an interactive visualization with several types of elements. These elements can include topologically associated domains (red), the copy number variant (green), genes with no phenotype matches (blue), genes with phenotype matches (orange), VISTA enhancers (purple), and DGV duplications (blue) and deletions (red). For the example case, both the <i>MCTP2</i> (left side) and <i>NR2F2</i> (right side) genes are highlighted in orange, indicating that they are associated with phenotypes that match to the patient. The last section of the page shows additional information for elements that are clicked on, in this case the <i>MCTP2</i> gene.\\n\\n <figure>\\n <div><picture>\\n <source></source></picture><p></p>\\n </div>\\n </figure></p>\",\"PeriodicalId\":40007,\"journal\":{\"name\":\"Current Protocols in Human Genetics\",\"volume\":\"108 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-12-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1002/cphg.91\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Current Protocols in Human Genetics\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/cphg.91\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Human Genetics","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cphg.91","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Cover: In Spector and Wiita. (http://doi.org/10.1002/cphg.106), the image shows a screenshot of ClinTAD's Single page for the example case. The top section of this page contains the input fields. The middle section contains an interactive visualization with several types of elements. These elements can include topologically associated domains (red), the copy number variant (green), genes with no phenotype matches (blue), genes with phenotype matches (orange), VISTA enhancers (purple), and DGV duplications (blue) and deletions (red). For the example case, both the MCTP2 (left side) and NR2F2 (right side) genes are highlighted in orange, indicating that they are associated with phenotypes that match to the patient. The last section of the page shows additional information for elements that are clicked on, in this case the MCTP2 gene.
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