{"id":4708,"date":"2020-06-21T06:15:44","date_gmt":"2020-06-21T06:15:44","guid":{"rendered":"http:\/\/blogs.sld.cu\/oserranob\/?p=4708"},"modified":"2020-06-21T06:15:44","modified_gmt":"2020-06-21T06:15:44","slug":"hallazgos-sobre-variaciones-geneticas-humanas","status":"publish","type":"post","link":"https:\/\/blogs.sld.cu\/oserranob\/2020\/06\/21\/hallazgos-sobre-variaciones-geneticas-humanas\/","title":{"rendered":"Hallazgos sobre variaciones gen\u00e9ticas humanas"},"content":{"rendered":"<p style=\"text-align: justify\">&#8211; <a title=\"Texto completo en ingl\u00e9s\" href=\"https:\/\/www.nature.com\/articles\/d41586-020-01485-4\" target=\"_blank\">Thousands of human sequences provide deep insight into single genomes<\/a><br \/>\n&#8211; <a title=\"Texto completo en ingl\u00e9s\" href=\"https:\/\/www.nature.com\/articles\/s41586-020-2267-z\" target=\"_blank\">Evaluating drug targets through human loss-of-function genetic variation<\/a><br \/>\n&#8211; <a title=\"Texto completo en ingl\u00e9s\" href=\"https:\/\/www.nature.com\/articles\/s41586-020-2308-7\" target=\"_blank\">The mutational constraint spectrum quantified from variation in 141,456 humans<\/a><br \/>\n&#8211; <a title=\"Texto completo en ingl\u00e9s\" href=\"https:\/\/www.nature.com\/immersive\/d42859-020-00002-x\/index.html\" target=\"_blank\">The Genome Aggregation Database (gnomAD)<\/a><br \/>\n&#8211; <a title=\"Texto completo en ingl\u00e9s\" href=\"https:\/\/www.pnas.org\/content\/early\/2020\/06\/01\/1917993117\" target=\"_blank\">Common homozygosity for predicted loss-of-function variants reveals both redundant and advantageous effects of dispensable human genes<\/a><br \/>\n&#8211; <a title=\"Texto completo en ingl\u00e9s\" href=\"https:\/\/www.cell.com\/cell\/fulltext\/S0092-8674(20)30619-X\" target=\"_blank\">Population Structure, Stratification, and Introgression of Human Structural Variation<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>&#8211; Thousands of human sequences provide deep insight into single genomes &#8211; Evaluating drug targets through human loss-of-function genetic variation &#8211; The mutational constraint spectrum quantified from variation in 141,456 humans &#8211; The Genome Aggregation Database (gnomAD) &#8211; Common homozygosity for predicted loss-of-function variants reveals both redundant and advantageous effects of dispensable human genes &#8211; [&hellip;]<\/p>\n","protected":false},"author":125,"featured_media":0,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[15,29],"tags":[],"_links":{"self":[{"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/posts\/4708"}],"collection":[{"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/users\/125"}],"replies":[{"embeddable":true,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/comments?post=4708"}],"version-history":[{"count":1,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/posts\/4708\/revisions"}],"predecessor-version":[{"id":4709,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/posts\/4708\/revisions\/4709"}],"wp:attachment":[{"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/media?parent=4708"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/categories?post=4708"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/tags?post=4708"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}