Enhance your data analysis experience with our new releases


QIAGEN Digital Insights

Enhance your data analysis experience with our new releases

We’re happy to announce that new releases of our products are now available. The releases offer a number of new features and improvements. You can see a few of the highlights below and visit the individual product pages to view the detailed release notes.


Determine which isoforms have interesting biological properties or enhance your multi-omics research approaches – here are the highlights of the latest IPA release:

  • Discover significant isoforms in RNA sequencing data with the enhanced IsoProfiler
    • Results are now expanded to include gene-level disease and function annotations
    • Focus on protein-coding transcripts with the new transcript type column for RefSeq datasets
  • Visualize phosphoproteomics data on networks and pathways
    • A new “phospho” measurement type is introduced


See the more detailed release notes:
IPA Fall Release 2016

Ingenuity Variant Analysis

With our fall release of Ingenuity Variant Analysis comes a number of improvements. The headlines are:

  • Expedite disease discovery using Phenotype-Driven Ranking filter
  • Evaluate variants using subpopulation Allele Frequency from ExAC
  • Incorporate CADD scores for functional predictions
  • Streamline Variant Analysis to QCI Interpret workflow

Get more details:
Ingenuity Variant Analysis Fall Release 2016

QCI Interpret

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

  • QCI Interpret is now integrated with Ingenuity Variant Analysis and provides large assay filtering and interpretation across these best-in-class tools
  • New “1-click” bibliography review: See the clinical literature relevant for each variant, including tools to normalize clinical cases appearing in multiple publications
  • Enhanced ACMG rules automation now with integrated population frequency data by ancestry and CADD predictions
  • Increased throughput of your clinical genetics and variant analysis capability for interpretation and reporting

See more feature improvements and details on the benefits:
QCI Interpret September 2016 Release

Workbenches and servers

It’s a pleasure to present the new releases of both workbenches and servers in our CLC product line. Here are a few highlights:

  • Improved accuracy and visualization for RNA-seq analysis
  • We now detect even larger deletions accurately
  • Analyze your data in the context of published research with the new SRA download
  • Now analyze genes and transcripts from both Ensembl and RefSeq

Read more about these and other new features and improvements:
Biomedical Genomics Workbench 3.5
Biomedical Genomics Server Solution 8.5
CLC Genomics Workbench 9.5
CLC Genomics Server 8.5