{"id":1870,"date":"2023-07-27T15:00:15","date_gmt":"2023-07-27T15:00:15","guid":{"rendered":"https:\/\/blogs.bmj.com\/jmg\/?p=1870"},"modified":"2026-02-23T00:01:02","modified_gmt":"2026-02-23T00:01:02","slug":"integrating-rna-seq-into-genome-sequencing-workflow-enhances-the-analysis-of-structural-variants-causing-neurodevelopmental-disorders","status":"publish","type":"post","link":"https:\/\/blogs.bmj.com\/jmg\/2023\/07\/27\/integrating-rna-seq-into-genome-sequencing-workflow-enhances-the-analysis-of-structural-variants-causing-neurodevelopmental-disorders\/","title":{"rendered":"Integrating RNA-Seq into genome sequencing workflow enhances the analysis of structural variants causing neurodevelopmental disorders (Contributed by Kevin Riquin)"},"content":{"rendered":"<p>Genetic testing plays a crucial role in diagnosing neurodevelopmental disorders (NDD). Geneticists continuously explore new methods, such as genome sequencing (GS), to improve diagnostic accuracy. However, some genetic variations detected by GS are challenging to understand. To address this, we combined GS with RNA-Seq, a technique that provides extra information about how these variations affect genes. Our study demonstrated that this innovative approach significantly enhances the diagnosis of NDD, particularly in complex cases. By integrating advanced techniques like RNA-Seq and optical genome mapping, we may soon have more reliable diagnostic tools for NDD, benefiting patients and advancing genetic research in healthcare. (<a href=\"https:\/\/jmg.bmj.com\/content\/early\/2023\/07\/26\/jmg-2023-109263\">https:\/\/jmg.bmj.com\/content\/early\/2023\/07\/26\/jmg-2023-109263<\/a> )<!--TrendMD v2.4.8--><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Genetic testing plays a crucial role in diagnosing neurodevelopmental disorders (NDD). Geneticists continuously explore new methods, such as genome sequencing (GS), to improve diagnostic accuracy. However, some genetic variations detected by GS are challenging to understand. To address this, we combined GS with RNA-Seq, a technique that provides extra information about how these variations affect [&#8230;]<\/p>\n<p><a class=\"btn btn-secondary understrap-read-more-link\" href=\"https:\/\/blogs.bmj.com\/jmg\/2023\/07\/27\/integrating-rna-seq-into-genome-sequencing-workflow-enhances-the-analysis-of-structural-variants-causing-neurodevelopmental-disorders\/\">Read More&#8230;<\/a><\/p>\n","protected":false},"author":123,"featured_media":0,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[1],"tags":[],"class_list":["post-1870","post","type-post","status-publish","format-standard","hentry","category-uncategorized"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.5 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Integrating RNA-Seq into genome sequencing workflow enhances the analysis of structural variants causing neurodevelopmental disorders (Contributed by Kevin Riquin) - JMG Contact blog<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/blogs.bmj.com\/jmg\/2023\/07\/27\/integrating-rna-seq-into-genome-sequencing-workflow-enhances-the-analysis-of-structural-variants-causing-neurodevelopmental-disorders\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Integrating RNA-Seq into genome sequencing workflow enhances the analysis of structural variants causing neurodevelopmental disorders (Contributed by Kevin Riquin) - JMG Contact blog\" \/>\n<meta property=\"og:description\" content=\"Genetic testing plays a crucial role in diagnosing neurodevelopmental disorders (NDD). Geneticists continuously explore new methods, such as genome sequencing (GS), to improve diagnostic accuracy. However, some genetic variations detected by GS are challenging to understand. To address this, we combined GS with RNA-Seq, a technique that provides extra information about how these variations affect [...]Read More...\" \/>\n<meta property=\"og:url\" content=\"https:\/\/blogs.bmj.com\/jmg\/2023\/07\/27\/integrating-rna-seq-into-genome-sequencing-workflow-enhances-the-analysis-of-structural-variants-causing-neurodevelopmental-disorders\/\" \/>\n<meta property=\"og:site_name\" content=\"JMG Contact blog\" \/>\n<meta property=\"article:published_time\" content=\"2023-07-27T15:00:15+00:00\" \/>\n<meta property=\"article:modified_time\" content=\"2026-02-23T00:01:02+00:00\" \/>\n<meta name=\"author\" content=\"hqqu\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:creator\" content=\"@HuiQiQu\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"hqqu\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"1 minute\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\\\/\\\/blogs.bmj.com\\\/jmg\\\/2023\\\/07\\\/27\\\/integrating-rna-seq-into-genome-sequencing-workflow-enhances-the-analysis-of-structural-variants-causing-neurodevelopmental-disorders\\\/#article\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/blogs.bmj.com\\\/jmg\\\/2023\\\/07\\\/27\\\/integrating-rna-seq-into-genome-sequencing-workflow-enhances-the-analysis-of-structural-variants-causing-neurodevelopmental-disorders\\\/\"},\"author\":{\"name\":\"hqqu\",\"@id\":\"https:\\\/\\\/blogs.bmj.com\\\/jmg\\\/#\\\/schema\\\/person\\\/be0250f8d5b52412c3e7c222dabd591b\"},\"headline\":\"Integrating RNA-Seq into genome sequencing workflow enhances the analysis of structural variants causing neurodevelopmental disorders (Contributed by Kevin Riquin)\",\"datePublished\":\"2023-07-27T15:00:15+00:00\",\"dateModified\":\"2026-02-23T00:01:02+00:00\",\"mainEntityOfPage\":{\"@id\":\"https:\\\/\\\/blogs.bmj.com\\\/jmg\\\/2023\\\/07\\\/27\\\/integrating-rna-seq-into-genome-sequencing-workflow-enhances-the-analysis-of-structural-variants-causing-neurodevelopmental-disorders\\\/\"},\"wordCount\":128,\"commentCount\":0,\"publisher\":{\"@id\":\"https:\\\/\\\/blogs.bmj.com\\\/jmg\\\/#organization\"},\"inLanguage\":\"en-US\",\"potentialAction\":[{\"@type\":\"CommentAction\",\"name\":\"Comment\",\"target\":[\"https:\\\/\\\/blogs.bmj.com\\\/jmg\\\/2023\\\/07\\\/27\\\/integrating-rna-seq-into-genome-sequencing-workflow-enhances-the-analysis-of-structural-variants-causing-neurodevelopmental-disorders\\\/#respond\"]}]},{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/blogs.bmj.com\\\/jmg\\\/2023\\\/07\\\/27\\\/integrating-rna-seq-into-genome-sequencing-workflow-enhances-the-analysis-of-structural-variants-causing-neurodevelopmental-disorders\\\/\",\"url\":\"https:\\\/\\\/blogs.bmj.com\\\/jmg\\\/2023\\\/07\\\/27\\\/integrating-rna-seq-into-genome-sequencing-workflow-enhances-the-analysis-of-structural-variants-causing-neurodevelopmental-disorders\\\/\",\"name\":\"Integrating RNA-Seq into genome sequencing workflow enhances the analysis of structural variants causing neurodevelopmental disorders (Contributed by Kevin Riquin) - 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