Sequencing Software

Achieve new levels of automation performance with the Thermo Scientific™ Momentum™ Workflow Scheduling software-  an industry-leading software platform that enables users to define, execute, and monitor scientific process... Read more...

Simultaneously profile gene expression and open chromatin from the same cell with Chromium Single Cell Multiome ATAC + Gene Expression. Multiply your power of discovery to characterize cell types and states, and uncover gene regulatory pr... Read more...

Complete toolkit for genomics, transcriptomics, epigenomics, and metagenomics in one program Read more...

Chromium Single Cell Gene Expression provides single cell transcriptome 3' gene expression and multiomic capabilities to profile tens of thousands of cells. Explore cellular heterogeneity, novel targets, and biomarkers with combined g... Read more...

The New Standard for Desktop-Based Bioinformatics Tools CLC DNA Workbench provides a software environment which enables users to perform advanced DNA sequence analyses such as assembly of DNA sequence data, graphically and algori... Read more...

Dominating the high-throughput sequencing data analysis challenge We have overcome the challenge to analyze high-throughput sequencing data faster than it is produced by implementing a SIMD-accelerated assembly algorithm in our next gene... Read more...

Looking for consistent and reproducible single cell results across experiments, across users, and even across multiple sites? With Chromium Connect, you can combine single cell partitioning, barcoding, and library preparation in a standar... Read more...

Bionano Data Solutions™ includes a complete suite of hardware and software for end-to-end experiment management, analysis and bioinformatics processing, along with convenient web-based management and monitoring tools. Read more...

Reliable detection of cancer-associated mutations in 597 genes from liquid biopsy samples Read more...

Comprehensive profile of all mutations present in the exome Read more...

Identify causal variants from human sequencing data in just hours Rapidly Identify and Prioritize Variants Ingenuity Variant Analysis combines analytical tools and integrated content to help you rapidly identify and prioritize varian... Read more...

Discover More, Sequence Less Built upon the NimbleGen Sequence Capture empirically optimized probe design algorithm with high efficiency uniformity of capture1, and now with expanded coverage of coding exons, SeqCap EZ Exome v3.0 offers ... Read more...

DeNovoX software automates and accelerates sequencing, returning results equal to or better than those formerly achieved through expert manual sequencing of peptides within proteins and is ideally suited for high-throughput analyses of pep... Read more...

Protein Analysis Software - the Next Generation CLC Protein Workbench creates a software environment enabling users to make a large number of advanced protein sequence analyses, combined with smooth data management, and excellent graph... Read more...

Free Bioinformatics Software Not a demo. Not scaled down. No spyware. No need to register. Yet still a wide variety of features available - and - free! CLC Free Workbench creates a software environment enabling users to make a larg... Read more...

CLC Combined Workbench includes all features and functions of CLC Free Workbench, CLC Protein Workbench, and CLC Gene Workbench.   The program sets new standards for bioinformatics software with its overall graphical display and usability ... Read more...

CLC bio presents its new software module for Multilocus Sequence Typing (MLST). MLST is a portable and precise state-of-the-art technique for typing bacteria and yeast isolates. It is based on DNA sequence data from a number of house-keepi... Read more...

With the all new CLC RNA Workbench, CLC bio brings you complex analysis of RNA molecules in a fully integrated, user-friendly and graphically advanced bioinformatics framework. Advanced The CLC RNA Workbench gives the user easy ac... Read more...

STRmix is sophisticated forensic software used to resolve mixed DNA profiles previously considered too complex to interpret. Read more...

Unlock the full potential of molecular diagnostics on a single platform Read more...

Agilent’s GeneSpring NGS software suite includes data analysis workflows for Methyl-Seq, RNA-Seq, DNA-Seq, Chip-Seq and Small RNA-Seq data. GeneSpring NGS provides SureSelect customers with an easy to use QC, visualization and reporting to... Read more...

Agilent's GeneSpring provides powerful, accessible statistical tools for intuitive data analysis and visualization.  Read more...

SureCall is a research desktop application combining both novel and widely accepted opensource algorithms for end-to-end NGS data analysis from alignment to categorization and annotation of mutations, supporting Agilent Target Enrichment ... Read more...

Interpret is OGT’s powerful and easy-to-use next-generation sequencing analysis solution. Read more...

QCI Interpret Translational is a NGS variant assessment software solution that enables rapid, evidence-powered variant annotation, filtering, and triage for human exome, genome, and large cohort sequencing data. Leveraging the QIAGEN... Read more...