{"id":10693,"date":"2020-01-21T15:51:05","date_gmt":"2020-01-21T15:51:05","guid":{"rendered":"https:\/\/www.dlongwood.com\/catalogo\/productos\/panel-de-nefropatias\/"},"modified":"2025-05-15T12:49:04","modified_gmt":"2025-05-15T12:49:04","slug":"nephropathy-solution","status":"publish","type":"productos","link":"https:\/\/www.dlongwood.com\/en\/product-catalog\/nephropathy-solution\/","title":{"rendered":"Nephropathy Solution (NES)"},"content":{"rendered":"\n<p>The <strong>Nephropathy Solution (NES)<\/strong> of Sophia Genetics covers the coding regions (\u00b1 5 bp of the intron regions) of <strong>44 most clinically relevant genes<\/strong> related to a broad range of nephropathies such as nephrotic syndromes, polycystic kidney diseases, Bartter syndromes, Alport syndrome, CAKUT or tubulopathies. <\/p>\n\n\n\n<p>It also allows the detection of <strong>SNV <\/strong>and <strong>Indels<\/strong>, and guarantees a high percentage of readings in the target and uniformity of coverage, even in regions rich in GC. <\/p>\n\n\n\n<p>The kit uses NGS capture technology and is intended for use on Illumina platforms. The results are interpreted in the<strong> SOPHiA DDM platform<\/strong>, designed for the analysis and protection of NGS clinical data in routine diagnosis. <\/p>\n\n\n\n<p>SOPHiA DDM analyzes complex NGS genomic data through the detection, annotation and pre-classification of genomic variants to help clinicians better diagnose their patients. <\/p>\n\n\n\n<figure class=\"wp-block-image size-large\"><img decoding=\"async\" src=\"https:\/\/dlongwood.com\/wp-content\/uploads\/2020\/01\/sophia-nefro-general-1024x129.jpg\" alt=\"\" class=\"wp-image-3352\" title=\"\"><figcaption><\/figcaption><\/figure>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity\"\/>\n\n\n\n<p>In addition to the Nephropathy Solution, we have other more specific panels for clinical diagnosis in areas such as metabolism, oncology, cardiology&#8230;<\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity\"\/>\n\n\n\n<figure class=\"wp-block-gallery has-nested-images columns-4 is-cropped wp-block-gallery-1 is-layout-flex wp-block-gallery-is-layout-flex\">\n<figure class=\"wp-block-image size-large\"><a href=\"https:\/\/dlongwood.com\/wp-content\/uploads\/2019\/11\/Sophia_panel_cancer_hereditario_NGS_carrusel_1.jpg\" target=\"_blank\" rel=\"noopener\"><img decoding=\"async\" data-id=\"1569\" src=\"https:\/\/dlongwood.com\/wp-content\/uploads\/2019\/11\/Sophia_panel_cancer_hereditario_NGS_carrusel_1.jpg\" alt=\"\" class=\"wp-image-1569\" title=\"\"><\/a><figcaption><\/figcaption><\/figure>\n\n\n\n<figure class=\"wp-block-image size-large\"><a href=\"https:\/\/dlongwood.com\/wp-content\/uploads\/2019\/11\/Sophia_panel_cancer_hereditario_NGS_carrusel_2.jpg\" target=\"_blank\" rel=\"noopener\"><img decoding=\"async\" data-id=\"1571\" src=\"https:\/\/dlongwood.com\/wp-content\/uploads\/2019\/11\/Sophia_panel_cancer_hereditario_NGS_carrusel_2.jpg\" alt=\"\" class=\"wp-image-1571\" title=\"\"><\/a><figcaption><\/figcaption><\/figure>\n\n\n\n<figure class=\"wp-block-image size-large\"><a href=\"https:\/\/dlongwood.com\/wp-content\/uploads\/2020\/01\/sophia-nefro-ri\u00f1on.png\" target=\"_blank\" rel=\"noopener\"><img decoding=\"async\" data-id=\"3355\" src=\"https:\/\/dlongwood.com\/wp-content\/uploads\/2020\/01\/sophia-nefro-ri\u00f1on.png\" alt=\"\" class=\"wp-image-3355\" title=\"\"><\/a><figcaption><\/figcaption><\/figure>\n\n\n\n<figure class=\"wp-block-image size-large\"><a href=\"https:\/\/dlongwood.com\/wp-content\/uploads\/2019\/11\/Sophia_panel_cancer_hereditario_NGS_carrusel_3.jpg\" target=\"_blank\" rel=\"noopener\"><img decoding=\"async\" data-id=\"1573\" src=\"https:\/\/dlongwood.com\/wp-content\/uploads\/2019\/11\/Sophia_panel_cancer_hereditario_NGS_carrusel_3.jpg\" alt=\"\" class=\"wp-image-1573\" title=\"\"><\/a><figcaption><\/figcaption><\/figure>\n<\/figure>\n","protected":false},"excerpt":{"rendered":"<p>Study of the 44 most clinically relevant genes related to nephropathies.<\/p>\n","protected":false},"featured_media":9291,"template":"","tecnologias":[36],"marcas":[215],"familias":[283,443,441],"class_list":["post-10693","productos","type-productos","status-publish","has-post-thumbnail","hentry","tecnologias-next-generation-sequencing-ngs","marcas-sophia-genetics-en","familias-molecular-genetics","familias-nephropathies","familias-targeted_study_of_specific_pathologies"],"_links":{"self":[{"href":"https:\/\/www.dlongwood.com\/en\/wp-json\/wp\/v2\/productos\/10693","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.dlongwood.com\/en\/wp-json\/wp\/v2\/productos"}],"about":[{"href":"https:\/\/www.dlongwood.com\/en\/wp-json\/wp\/v2\/types\/productos"}],"version-history":[{"count":0,"href":"https:\/\/www.dlongwood.com\/en\/wp-json\/wp\/v2\/productos\/10693\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.dlongwood.com\/en\/wp-json\/wp\/v2\/media\/9291"}],"wp:attachment":[{"href":"https:\/\/www.dlongwood.com\/en\/wp-json\/wp\/v2\/media?parent=10693"}],"wp:term":[{"taxonomy":"tecnologias","embeddable":true,"href":"https:\/\/www.dlongwood.com\/en\/wp-json\/wp\/v2\/tecnologias?post=10693"},{"taxonomy":"marcas","embeddable":true,"href":"https:\/\/www.dlongwood.com\/en\/wp-json\/wp\/v2\/marcas?post=10693"},{"taxonomy":"familias","embeddable":true,"href":"https:\/\/www.dlongwood.com\/en\/wp-json\/wp\/v2\/familias?post=10693"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}