{"id":9042,"date":"2019-10-11T10:20:48","date_gmt":"2019-10-11T10:20:48","guid":{"rendered":"https:\/\/www.dlongwood.com\/mieloyd-solution\/"},"modified":"2025-05-22T08:27:33","modified_gmt":"2025-05-22T08:27:33","slug":"myeloid-solution","status":"publish","type":"productos","link":"https:\/\/www.dlongwood.com\/en\/product-catalog\/myeloid-solution\/","title":{"rendered":"Myeloid panels"},"content":{"rendered":"\n<p>The <strong>Myeloid Solution<\/strong> by SOPHiA GENETICS is designed for the identification of mutations in 30 genes associated with Myelodysplastic Syndromes, Myeloproliferative Neoplasms and Leukemia, by Next-Generation Sequencing (NGS).<\/p>\n\n\n\n<p>This diagnostic solution facilitates the selection of a personalized treatment, based on the genetic profile of each patient.<\/p>\n\n\n\n<p> Genes and their association with diseases: <\/p>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter\"><img decoding=\"async\" src=\"https:\/\/dlongwood.com\/wp-content\/uploads\/2019\/10\/tabla_genes.png\" alt=\"Tabla de genes\" class=\"wp-image-689\" title=\"\"><\/figure><\/div>\n\n\n\n<p>In addition to an accurate analysis of the key markers<strong> CEBPA, FLT3 <\/strong>(ITDs duplications) and <strong>CALR <\/strong>(large deletions), the kit allows the detection of <strong>SNVs, Indels <\/strong>and <strong>CNVs<\/strong>.<\/p>\n\n\n\n<hr class=\"wp-block-separator\"\/>\n\n\n\n<p> <strong>MYSplus panel <\/strong>is also available, which includes, in addition to the standard panel,<strong> RNA analysis for over 100 gene fusions<\/strong>. <\/p>\n\n\n\n<hr class=\"wp-block-separator\"\/>\n\n\n\n<p>Both, <strong>MYS<\/strong> and <strong>MYSplus kits<\/strong>, are based on NGS capture technology. The results are interpreted on the <strong>SOPHiA DDM<\/strong> platform, designed for the analysis and protection of NGS clinical data in the routine diagnosis.<\/p>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter\"><img decoding=\"async\" src=\"https:\/\/dlongwood.com\/wp-content\/uploads\/2019\/10\/ids_step-1024x253.png\" alt=\"ids step\" class=\"wp-image-694\" title=\"\"><\/figure><\/div>\n\n\n\n<p>In addition to the <strong>Myeloid Solutions<\/strong>, other panels for clinical diagnosis in areas such as metabolism, oncology, genetics and cardiology are available.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Identification of mutations associated to Myelodysplasic Syndroms, Myeloproliferative Neoplasms and Leukemia.<\/p>\n","protected":false},"featured_media":9048,"template":"","tecnologias":[36],"marcas":[215],"familias":[340,336],"class_list":["post-9042","productos","type-productos","status-publish","has-post-thumbnail","hentry","tecnologias-next-generation-sequencing-ngs","marcas-sophia-genetics-en","familias-myeloid-line","familias-oncohematology"],"_links":{"self":[{"href":"https:\/\/www.dlongwood.com\/en\/wp-json\/wp\/v2\/productos\/9042","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\/9042\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.dlongwood.com\/en\/wp-json\/wp\/v2\/media\/9048"}],"wp:attachment":[{"href":"https:\/\/www.dlongwood.com\/en\/wp-json\/wp\/v2\/media?parent=9042"}],"wp:term":[{"taxonomy":"tecnologias","embeddable":true,"href":"https:\/\/www.dlongwood.com\/en\/wp-json\/wp\/v2\/tecnologias?post=9042"},{"taxonomy":"marcas","embeddable":true,"href":"https:\/\/www.dlongwood.com\/en\/wp-json\/wp\/v2\/marcas?post=9042"},{"taxonomy":"familias","embeddable":true,"href":"https:\/\/www.dlongwood.com\/en\/wp-json\/wp\/v2\/familias?post=9042"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}