IPA

A powerful analysis and search tool that uncovers the significance of ‘omics data and identifies new targets or candidate biomarkers within.

CLC Genomics Workbench

CLC Genomics Workbench is a powerful solution for analyzing and visualizing NGS data, incorporating cutting-edge technology and algorithms.

CLC Assembly Cell

CLC Assembly Cell is a high-performance computing solution for read mapping and de novo assembling of next-generation sequencing data.

CLC Main Workbench

CLC Main Workbench is a comprehensive analysis package for advanced DNA, RNA, and protein analyses, all wrapped in an intuitive graphical user-interface.

CLC Genomics Server

CLC Genomics Server provides a solution for building and managing a modern and efficient enterprise-wide bioinformatics platform in organizations of any size.

ANNOVAR

ANNOVAR is an efficient command line Perl program to functionally annotate genetic variants from high-throughput sequencing data.

Inova Genomes

Inova Genomes provides access to high quality pre-annotated and pre-computed experimental data for easy and rapid hypothesis generation and validation.

CLC Server Command Line Tools

A client interface for CLC Server products, to run server-based analyses, workflows, and various other data operations via the command line or included in scripts.

CLC Sequence Viewer

A software environment enabling you to make a large number of bioinformatics analyses, combined with smooth data management, and excellent graphical options.

CLC Microbial Genomics Module

CLC Microbial Genomics Module combines efficient algorithms, interactive visualization, and powerful statistical tools for microbial genomics data analysis.

CLC Genome Finishing Module

CLC Genome Finishing Module is an add-on to CLC Genomics Workbench, designed to accelerate and simplify genome finishing.

Find all our modules and plug-ins here

QCI Interpret – somatic

An integrated clinical decision support solution designed specifically for routine somatic cancer testing laboratories assessing NGS data.

QCI Interpret – hereditary

QCI Interpret for Hereditary Cancer is a comprehensive clinical decision support solution with manually curated scientific evidence for germline cancers.

HGMD

HGMD Professional is a unique resource providing comprehensive data on human inherited disease mutations to genetics and genomic research.

Biomedical Genomics Workbench

Accelerate NGS data interpretation and uncover meaningful insights in cancer, hereditary and rare diseases research with Biomedical Genomics Workbench.

Biomedical Genomics Server Solution

Biomedical Genomics Server provides a solution for building and managing a modern enterprise-wide platform for organizations of any size.

Ingenuity Variant Analysis

Ingenuity Variant Analysis combines analytical tools and integrated content to help you rapidly identify and prioritize variants from human sequencing data.

Find all our modules and plug-ins here