Next Generation Sequencing Data Analysis, Data visualization tool | Avadis NGS

What is Avadis NGS?

Avadis NGS provides comprehensive workflows for analysis, visualization and management of NGS data on a wide range of computing infrastructures. The new server version provides scalable compute, centralizes storage and enables collaboration for larger groups

The user-friendly Avadis® platform powers all bioinformatics products developed by Strand.The platform has been enhanced with state-of-the-art algorithms for analysis, visualization and management of next-generation sequencing data on a wide range of computing infrastructures. More

  • 1 Solve the mysteries of biology with Avadis NGS

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  • 1 Find expression levels of small RNA genes
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  • 1 Align sequence data from DNA-Seq, ChIP-Seq, RNA-Seq, and Small RNA-Seq experiments
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  • 1 Identify targets of miRNAs common to multiple databases
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  • 1 Identify significant SNPs using an intuitive filtering framework
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  • 1 Visualize billions of reads in the Genome Browser
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  • 1 Easily download organism annotations in the Annotations Manager
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  • 1 Find transcription factor binding sites with ChIP-Seq experiments
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  • 1 Find and filter out reads with poor mapping and alignment qualities
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  • 1 Determine regulation of gene expression from multiple RNA-Seq samples
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  • 1 Locate large structural variants in DNA-Seq data
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  • 1 Find novel splice junctions with RNA-Seq experiments
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  • 1 Determine genes overlapping in entity lists
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  • 1 Contextualize biological information with built-in pathways and GO analysis
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  • 1 Enable collaborative analysis and utilize your resources optimally using Avadis NGS Server Edition
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Free 20-Day Trial

Experience a new standard in NGS bioinformatics. We'll provide you with the annotations you need to analyze your SAM/BAM, ELAND or FASTQ files.

Latest Updates

Strand Releases Enterprise Server Edition to AvadisNGS, Establishes Reads to Reporting Solution for Clinical Genomics Read
Strand Genomics Announces Availability Of Technology Solutions To Power Expansion Of Personalized Medicine Centers In U.S. Read

Archived Webinars:

Watch a recording of our most recent webinar on 'RNA Seq Data Analysis', as well as for other webinars in our archived webinars segment

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Recent Updates

  • White paper on 'Avadis NGS DNA Read Aligner - A Benchmarking study' by Dr.Rohit Gupta et al Read

  • Announcing the release of version 1.6! Read the release notes

  • Recent publications citing Avadis NGS. Read

  • Read the latest blog by Dr.Vamsi Read

  • Recent Newsletters and Announcements. Read