{"id":3609,"date":"2015-03-27T21:13:11","date_gmt":"2015-03-27T21:13:11","guid":{"rendered":"http:\/\/www.cytognomix.com\/?p=3609"},"modified":"2015-03-27T21:14:44","modified_gmt":"2015-03-27T21:14:44","slug":"march-27-2015-cover-of-the-f1000research-webpage","status":"publish","type":"post","link":"https:\/\/www.cytognomix.com\/?p=3609","title":{"rendered":"March 27, 2015. Cover of the F1000Research webpage"},"content":{"rendered":"<p>Our paper, &#8220;<a title=\"Interpretation of mRNA splicing mutations....\" href=\"http:\/\/f1000research.com\/articles\/3-282\/v2\" target=\"_blank\">Interpretation of mRNA splicing mutations in genetic disease: review of the literature and guidelines for information-theoretical analysis<\/a>,&#8221; and video, \u00a0&#8220;<a title=\"Video blog post on interpreting of genomic variants\" href=\"http:\/\/blog.f1000research.com\/2015\/03\/17\/interpreting-genomic-variants-in-rare-and-common-diseases\/\" target=\"_blank\" class=\"broken_link\">Interpreting genomic variants in rare and common diseases<\/a>,&#8221; have been highlighted by <a title=\"F1000Research Journal\" href=\"http:\/\/f1000research.com\" target=\"_blank\">F1000Research<\/a> on their home page.<\/p>\n<p><a href=\"http:\/\/www.cytognomix.com\/wp-content\/uploads\/2015\/03\/Cover.jpg\"><img loading=\"lazy\" class=\"alignleft  wp-image-3610\" alt=\"Cover\" src=\"http:\/\/www.cytognomix.com\/wp-content\/uploads\/2015\/03\/Cover.jpg\" width=\"649\" height=\"558\" srcset=\"https:\/\/www.cytognomix.com\/wp-content\/uploads\/2015\/03\/Cover.jpg 984w, https:\/\/www.cytognomix.com\/wp-content\/uploads\/2015\/03\/Cover-300x257.jpg 300w, https:\/\/www.cytognomix.com\/wp-content\/uploads\/2015\/03\/Cover-900x772.jpg 900w\" sizes=\"(max-width: 649px) 100vw, 649px\" \/><\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Our paper, &#8220;Interpretation of mRNA splicing mutations in genetic disease: review of the literature and guidelines for information-theoretical analysis,&#8221; and video, \u00a0&#8220;Interpreting genomic variants in rare and common diseases,&#8221; have been highlighted by F1000Research on their home page.<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[],"_links":{"self":[{"href":"https:\/\/www.cytognomix.com\/index.php?rest_route=\/wp\/v2\/posts\/3609"}],"collection":[{"href":"https:\/\/www.cytognomix.com\/index.php?rest_route=\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.cytognomix.com\/index.php?rest_route=\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.cytognomix.com\/index.php?rest_route=\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.cytognomix.com\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=3609"}],"version-history":[{"count":3,"href":"https:\/\/www.cytognomix.com\/index.php?rest_route=\/wp\/v2\/posts\/3609\/revisions"}],"predecessor-version":[{"id":3613,"href":"https:\/\/www.cytognomix.com\/index.php?rest_route=\/wp\/v2\/posts\/3609\/revisions\/3613"}],"wp:attachment":[{"href":"https:\/\/www.cytognomix.com\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=3609"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.cytognomix.com\/index.php?rest_route=%2Fwp%2Fv2%2Fcategories&post=3609"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.cytognomix.com\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=3609"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}