{"id":3401,"date":"2014-06-12T12:21:04","date_gmt":"2014-06-12T12:21:04","guid":{"rendered":"http:\/\/www.cytognomix.com\/?page_id=3401"},"modified":"2022-03-25T23:31:12","modified_gmt":"2022-03-25T23:31:12","slug":"mutationforecaster","status":"publish","type":"page","link":"https:\/\/www.cytognomix.com\/?page_id=3401","title":{"rendered":"Mutation Forecaster\u00ae"},"content":{"rendered":"

MutationForecaster\u00ae<\/a><\/em><\/strong>\u00a0(mutationforecaster.com<\/a>) is Cytognomix’s patented web-portal for\u00a0analysis<\/span>\u00a0of all types of mutations (coding and non-coding), including interpretation, comparison and management of genetic variant data.\u00a0It’s a fully automated genome interpretation solution for research, translational and clinical labs.\u00a0 \u00a0<\/span><\/p>\n

MutationForecaster\u00ae<\/strong> <\/em>combines our world-leading genome interpretation software\u00a0<\/span>on your exome, gene panel, or complete genome (Shannon transcription factor and splicing pipelines, ASSEDA, Veridical) with the Cytognomix User Variation Database<\/span> and \u00a0Variant Effect Predictor<\/span>. \u00a0With our integrated suite of software products, analyze coding, non-coding, and copy number variants, and compare new results with existing or your own database. \u00a0Select\u00a0predicted mutations \u00a0by phenotype using<\/span>\u00a0articles with Cyto<\/span> V<\/span>isualization A<\/span>nalytics. \u00a0With Workflows<\/span>, \u00a0automatically perform end-to-end analysis with all of our software products.\u00a0<\/span><\/p>\n

Download an 1 page overview of\u00a0MutationForecaster<\/strong>\u00ae<\/strong><\/em>:\u00a0link<\/a>\u00a0.<\/p>\n

You can now experience our integrated suite of genome interpretation products through a\u00a0free<\/em>\u00a0trial of<\/strong> MutationForecaster\u00ae<\/a>. Once you register, analyze datasets that we have analyzed in our peer-reviewed publications<\/em> with any of our software tools.<\/p>\n

To obtain a subscription (2 months or 1 year [pricing<\/a>]) to MutationForecaster\u00ae,<\/a> please contact us<\/a>.\u00a0\u00a0<\/p>\n

Don’t want to run your own analyses? Let us do it for you with our Bespoke Analysis Service<\/a>.<\/p>\n

\"mutforecast\"<\/a>

mutationforecaster.com<\/p><\/div>\n

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MutationForecaster\u00ae\u00a0(mutationforecaster.com) is Cytognomix’s patented web-portal for\u00a0analysis\u00a0of all types of mutations (coding and non-coding), including interpretation, comparison and management of genetic variant data.\u00a0It’s a fully automated genome interpretation solution for research, translational and clinical labs.\u00a0 \u00a0 MutationForecaster\u00ae combines our world-leading genome interpretation software\u00a0on your exome, gene panel, or complete genome (Shannon transcription factor and splicing pipelines, […]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":[],"tags":[113,170,120,127,173,129,174,177,161,125,171],"_links":{"self":[{"href":"https:\/\/www.cytognomix.com\/index.php?rest_route=\/wp\/v2\/pages\/3401"}],"collection":[{"href":"https:\/\/www.cytognomix.com\/index.php?rest_route=\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.cytognomix.com\/index.php?rest_route=\/wp\/v2\/types\/page"}],"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=3401"}],"version-history":[{"count":38,"href":"https:\/\/www.cytognomix.com\/index.php?rest_route=\/wp\/v2\/pages\/3401\/revisions"}],"predecessor-version":[{"id":5021,"href":"https:\/\/www.cytognomix.com\/index.php?rest_route=\/wp\/v2\/pages\/3401\/revisions\/5021"}],"wp:attachment":[{"href":"https:\/\/www.cytognomix.com\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=3401"}],"wp:term":[{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.cytognomix.com\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=3401"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}