We'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

IPA<\/h4>\n

Determine which isoforms have interesting biological properties or\u00a0enhance your multi-omics research approaches - here are the highlights of the latest IPA release:<\/p>\n

\n

\n
• Discover significant isoforms in RNA sequencing data with the enhanced IsoProfiler\n
  \n
  • Results are now expanded to include gene-level disease and function annotations<\/li>\n
  • Focus on protein-coding transcripts with the new transcript type column for RefSeq datasets<\/li>\n<\/ul>\n<\/li>\n
  • Visualize phosphoproteomics data on networks and pathways\n
    \n
    • A new \u201cphospho\u201d measurement type is introduced<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<\/div>\n

       <\/p>\n

      See the more detailed release notes:
      \nIPA Fall Release 2016<\/p>\n

      Ingenuity Variant Analysis<\/h4>\n

      \n

      With our fall release of Ingenuity Variant Analysis comes a number of improvements. The headlines are:<\/p>\n

      \n
      • Expedite disease discovery using Phenotype-Driven Ranking filter<\/li>\n
      • Evaluate variants using subpopulation Allele Frequency from ExAC<\/li>\n
      • Incorporate CADD scores for functional predictions<\/li>\n
      • Streamline Variant Analysis to QCI Interpret workflow<\/li>\n<\/ul>\n
        <\/div>\n

        Get more details:
        \nIngenuity Variant Analysis Fall Release 2016<\/p>\n<\/div>\n

        \n

        <\/h4>\n

        QCI\u00a0Interpret<\/h4>\n

        Take a look at these highlights of features and benefits you get from the QIAGEN Clinical Insight (QCI) Interpret September 2016 release:<\/p>\n

        \n
        • QCI Interpret is now integrated with Ingenuity Variant Analysis and provides large assay filtering and interpretation across these best-in-class tools<\/li>\n
        • 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
        • Enhanced ACMG rules automation now with integrated population frequency data by ancestry and CADD predictions<\/li>\n
        • Increased throughput of your clinical genetics and variant analysis capability for interpretation and reporting<\/li>\n<\/ul>\n

          See more feature improvements and details on the benefits:
          \nQCI Interpret September 2016 Release<\/p>\n<\/div>\n

          Workbenches and servers<\/h4>\n

          It'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

          \n
          • Improved accuracy\u00a0and visualization for RNA-seq analysis<\/li>\n
          • We now detect even larger deletions\u00a0accurately<\/li>\n
          • Analyze your data in the context of published research with the new SRA download<\/li>\n
          • Now analyze genes and transcripts from both Ensembl and\u00a0RefSeq<\/li>\n<\/ul>\n

            Read more about these and other new features and improvements:
            \nBiomedical Genomics Workbench\u00a03.5
            \nBiomedical Genomics Server Solution 8.5
            \nCLC Genomics Workbench\u00a09.5
            \nCLC Genomics Server\u00a08.5<\/p>\n","protected":false},"excerpt":{"rendered":"We'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 […]","protected":false},"author":5,"featured_media":151869,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"ct_builder_shortcodes":"","ct_template_type":"","ct_parent_template":0,"_EventAllDay":false,"_EventTimezone":"","_EventStartDate":"","_EventEndDate":"","_EventStartDateUTC":"","_EventEndDateUTC":"","_EventShowMap":false,"_EventShowMapLink":false,"_EventURL":"","_EventCost":"","_EventCostDescription":"","_EventCurrencySymbol":"","_EventCurrencyCode":"","_EventCurrencyPosition":"","_EventDateTimeSeparator":"","_EventTimeRangeSeparator":"","_EventOrganizerID":[],"_EventVenueID":[],"_OrganizerEmail":"","_OrganizerPhone":"","_OrganizerWebsite":"","_VenueAddress":"","_VenueCity":"","_VenueCountry":"","_VenueProvince":"","_VenueState":"","_VenueZip":"","_VenuePhone":"","_VenueURL":"","_VenueStateProvince":"","_VenueLat":"","_VenueLng":"","_VenueShowMap":false,"_VenueShowMapLink":false,"_tribe_blocks_recurrence_rules":"","_tribe_blocks_recurrence_description":"","_tribe_blocks_recurrence_exclusions":"","footnotes":""},"categories":[10956],"tags":[11099,68,11055,51,11209,11008],"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":"\n