{"id":150,"date":"2022-06-27T14:38:21","date_gmt":"2022-06-27T12:38:21","guid":{"rendered":"https:\/\/neuropediatoolbox.wordpress.com\/?p=150"},"modified":"2022-09-26T08:38:04","modified_gmt":"2022-09-26T08:38:04","slug":"predwes","status":"publish","type":"post","link":"https:\/\/neuropediatoolkit.org\/en\/predwes\/","title":{"rendered":"PredWES"},"content":{"rendered":"\n<p><a href=\"https:\/\/humandiseasegenes.nl\/predwes\">PredWES<\/a> es una herramienta de c\u00e1lculo de probabilidad de resultados positivos en los estudios de secuenciaci\u00f3n del exoma en funci\u00f3n de los hallazgos cl\u00ednicos. 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id=\"zp-ID-150-332710-XTMW6XMI\" data-zp-author-date='Wright-et-al.-2018-02-05' data-zp-date-author='2018-02-05-Wright-et-al.' data-zp-date='2018-02-05' data-zp-year='2018' data-zp-itemtype='journalArticle' class=\"zp-Entry zpSearchResultsItem\">\n<div class=\"csl-bib-body\" style=\"line-height: 1.35; \">\n  <div class=\"csl-entry\" style=\"clear: left; \">\n    <div class=\"csl-left-margin\" style=\"float: left; padding-right: 0.5em; text-align: right; width: 1em;\">1.<\/div><div class=\"csl-right-inline\" style=\"margin: 0 .4em 0 1.5em;\">Wright CF, FitzPatrick DR, Firth HV. Paediatric genomics: diagnosing rare disease in children. Nature Reviews Genetics [Internet]. 2018 Feb 5 [cited 2018 Feb 19]; Available from: <a class='zp-ItemURL' href='http:\/\/www.nature.com\/doifinder\/10.1038\/nrg.2017.116'>http:\/\/www.nature.com\/doifinder\/10.1038\/nrg.2017.116<\/a><\/div>\n  <\/div>\n<\/div>\n\t\t\t\t<\/div><!-- .zp-Entry .zpSearchResultsItem -->\n\t\t\t<\/div><!-- .zp-zp-SEO-Content -->\n\t\t<\/div><!-- .zp-List -->\n\t<\/div><!--.zp-Zotpress-->\n\n<\/figcaption><\/figure>\n","protected":false},"excerpt":{"rendered":"<p>PredWES es una herramienta de c\u00e1lculo de probabilidad de resultados positivos en los estudios de secuenciaci\u00f3n del exoma en funci\u00f3n de los hallazgos cl\u00ednicos. Puede utilizarse para la toma de decisiones basadas en la evidencia a la hora de solicitar estudios gen\u00e9ticos. Indicaciones para la realizaci\u00f3n de secuenciaci\u00f3n NGS:<\/p>","protected":false},"author":1,"featured_media":2502,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"image","meta":{"_themeisle_gutenberg_block_has_review":false,"footnotes":""},"categories":[10],"tags":[],"class_list":["post-150","post","type-post","status-publish","format-image","has-post-thumbnail","hentry","category-neurogenetica","post_format-post-format-image","entry"],"_links":{"self":[{"href":"https:\/\/neuropediatoolkit.org\/en\/wp-json\/wp\/v2\/posts\/150","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/neuropediatoolkit.org\/en\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/neuropediatoolkit.org\/en\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/neuropediatoolkit.org\/en\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/neuropediatoolkit.org\/en\/wp-json\/wp\/v2\/comments?post=150"}],"version-history":[{"count":0,"href":"https:\/\/neuropediatoolkit.org\/en\/wp-json\/wp\/v2\/posts\/150\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/neuropediatoolkit.org\/en\/wp-json\/wp\/v2\/media\/2502"}],"wp:attachment":[{"href":"https:\/\/neuropediatoolkit.org\/en\/wp-json\/wp\/v2\/media?parent=150"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/neuropediatoolkit.org\/en\/wp-json\/wp\/v2\/categories?post=150"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/neuropediatoolkit.org\/en\/wp-json\/wp\/v2\/tags?post=150"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}