{"id":11574,"date":"2016-09-16T13:07:06","date_gmt":"2016-09-16T13:07:06","guid":{"rendered":"https:\/\/staging.digitalinsights.supremeclients.com\/?p=11574"},"modified":"2020-04-28T12:01:23","modified_gmt":"2020-04-28T12:01:23","slug":"enhance-data-analysis-experience-new-releases","status":"publish","type":"post","link":"https:\/\/staging.digitalinsights.supremeclients.com\/news\/blog\/discovery\/enhance-data-analysis-experience-new-releases\/","title":{"rendered":"Enhance your data analysis experience with our new releases"},"content":{"rendered":"<p>We&#8217;re happy\u00a0to announce that new\u00a0releases of\u00a0our products are now available. The releases offer a number of new features\u00a0and\u00a0improvements. You can see a few of the highlights below and visit the individual product pages to view the detailed release notes.<\/p>\n<h4>IPA<\/h4>\n<p>Determine which isoforms have interesting biological properties or\u00a0enhance your multi-omics research approaches &#8211; here are the highlights of the latest IPA release:<\/p>\n<div>\n<ul>\n<li>Discover significant isoforms in RNA sequencing data with the enhanced IsoProfiler\n<ul>\n<li>Results are now expanded to include gene-level disease and function annotations<\/li>\n<li>Focus on protein-coding transcripts with the new transcript type column for RefSeq datasets<\/li>\n<\/ul>\n<\/li>\n<li>Visualize phosphoproteomics data on networks and pathways\n<ul>\n<li>A new \u201cphospho\u201d measurement type is introduced<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<\/div>\n<p>&nbsp;<\/p>\n<p>See the more detailed release notes:<br \/>\nIPA Fall Release 2016<\/p>\n<h4>Ingenuity Variant Analysis<\/h4>\n<div>\n<p>With our fall release of Ingenuity Variant Analysis comes a number of improvements. The headlines are:<\/p>\n<ul>\n<li>Expedite disease discovery using Phenotype-Driven Ranking filter<\/li>\n<li>Evaluate variants using subpopulation Allele Frequency from ExAC<\/li>\n<li>Incorporate CADD scores for functional predictions<\/li>\n<li>Streamline Variant Analysis to QCI Interpret workflow<\/li>\n<\/ul>\n<div><\/div>\n<p>Get more details:<br \/>\nIngenuity Variant Analysis Fall Release 2016<\/p>\n<\/div>\n<div>\n<h4><\/h4>\n<h4>QCI\u00a0Interpret<\/h4>\n<p>Take a look at these highlights of features and benefits you get from the QIAGEN Clinical Insight (QCI) Interpret September 2016 release:<\/p>\n<ul>\n<li>QCI Interpret is now integrated with Ingenuity Variant Analysis and provides large assay filtering and interpretation across these best-in-class tools<\/li>\n<li>New \u201c1-click\u201d bibliography review: See the clinical literature relevant for each variant, including tools to normalize clinical cases appearing in multiple publications<\/li>\n<li>Enhanced ACMG rules automation now with integrated population frequency data by ancestry and CADD predictions<\/li>\n<li>Increased throughput of your clinical genetics and variant analysis capability for interpretation and reporting<\/li>\n<\/ul>\n<p>See more feature improvements and details on the benefits:<br \/>\nQCI Interpret September 2016 Release<\/p>\n<\/div>\n<h4>Workbenches and servers<\/h4>\n<p>It&#8217;s a pleasure to present the new releases of both workbenches and servers in our CLC product line. Here are a few highlights:<\/p>\n<ul>\n<li>Improved accuracy\u00a0and visualization for RNA-seq analysis<\/li>\n<li>We now detect even larger deletions\u00a0accurately<\/li>\n<li>Analyze your data in the context of published research with the new SRA download<\/li>\n<li>Now analyze genes and transcripts from both Ensembl and\u00a0RefSeq<\/li>\n<\/ul>\n<p>Read more about these and other new features and improvements:<br \/>\nBiomedical Genomics Workbench\u00a03.5<br \/>\nBiomedical Genomics Server Solution 8.5<br \/>\nCLC Genomics Workbench\u00a09.5<br \/>\nCLC Genomics Server\u00a08.5<\/p>\n","protected":false},"excerpt":{"rendered":"We&#8217;re happy\u00a0to announce that new\u00a0releases of\u00a0our products are now available. The releases offer a number of new features\u00a0and\u00a0improvements. You can&#8230;","protected":false},"author":18,"featured_media":11609,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[2],"tags":[84,14,114,49,239,44],"class_list":["post-11574","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-discovery","tag-biomedical-genomics-server-solution","tag-biomedical-genomics-workbench","tag-clc-genomics-server","tag-clc-genomics-workbench","tag-clc-main-workbench","tag-release"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v23.8 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Enhance your data analysis experience with our new releases - Bioinformatics Software | QIAGEN Digital Insights<\/title>\n<meta name=\"robots\" content=\"noindex, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Enhance your data analysis experience with our new releases - Bioinformatics Software | QIAGEN Digital Insights\" \/>\n<meta property=\"og:description\" content=\"We&#8217;re happy\u00a0to announce that new\u00a0releases of\u00a0our products are now available. 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