Strand NGS (Formerly Avadis NGS) is an integrated platform that provides analysis, management and visualization tools for next-generation sequencing data. It supports extensive workflows for alignment, RNA-Seq, small RNA-Seq, DNA-Seq, Methyl-Seq, and ChIP-Seq experiments.

Strand NGS (Formerly Avadis NGS) is an integrated platform that provides analysis, management and visualization tools for next-generation sequencing data. It supports extensive workflows for alignment, RNA-Seq, small RNA-Seq, DNA-Seq, Methyl-Seq, and ChIP-Seq experiments.

Sequence to science

Vivek Jayaswal

deep analysis and better insights

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RNA-Seq

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RNA-Seq

Differential gene expression, identify novel genes, exons, novel splice junctions and more

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DNA-Seq

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DNA-Seq

Detect variants, identify effect on transcripts, structural variants, CNVs, and more

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ChIP-Seq

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ChIP-Seq

Identify transcription factor binding sites and histone modification sites using the PICS and MACS

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Small RNA-Seq

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Small RNA-Seq

Detect differentially expressed small RNAs, novel small RNA genes, identify mRNA targets and more

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Methyl-Seq

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Methyl-Seq

Detect differentially methylated regions/cytosines and study methylation effects

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More Features

Alignment & Data QC

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Alignment & Data QC

Find and filter out reads with poor mapping and alignment qualities

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Rich visualizations

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Rich visualizations

Identify poor quality reads, mapping quality, variant support views, coverage and other visualizations

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Genome browser

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Genome browser

Visualize annotations, multiple genomics regions at different zoom levels

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Server Edition

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Server Edition

Designed to cater to the needs of multi-member teams working on NGS data analysis

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Biological Interpretation

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Biological Interpretation

Learn how genes interact with each other using information from literature and canonical pathways

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Free
20-Day
Trial

Starting your trial is easy.

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sales@strandngs.com
USA: 1-800-752-9122
ROW: +1-650-353-5060
support@strandngs.com
USA: 1-800-516-5181
ROW: +1-650-288-4559