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Genomics Suite

Next-gen sequencing software for thorough data analysis.

RNA-Seq analysis in GenVision Pro

DNASTAR’s Genomics Suite provides everything you need for next-gen sequencing including assembly, alignment, and analysis.  Simplified next gen software, integrated into a single package.  The suite supports all major traditional and next-generation sequencing technologies, including Illumina and Ion Torrent, making it easy to work with your data for any type of project.  Find out why our software is #1 in accuracy for variant detection and SNP analysis.

Licensing Options  Technical Requirements  File Formats

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Powered by Bioz

Supported Workflows

Automated Genome Closure

ChIP-Seq Analysis

Combined Analysis for NGS Projects

De Novo Genome Assembly

De Novo Transcriptome Assembly

Genomic Visualization

Mendelian Gene Panels and Exome Analysis

Metagenomics

Reference-Guided Genome Alignment

RNA-Seq Alignment

SNP to Structure Analysis

SNP Validation Control

Variant Analysis

gene resequencing results

Analysis Software for All Major Next-Gen Sequencing Technologies

Illumina sequencing
Ion Torrent Sequencing
PacBio Sequencing

Included Applications and Features

SeqMan NGen

Accurate Alignment and Assembly of Genomic Sequencing Data

  • Assemble genome and transcriptome data from all major NGS and Sanger sequencing platforms.
  • Align RNA-Seq, ChIP-Seq, miRNA, exome and whole genome sequencing data, and any combination of various project types.
  • Open results in SeqMan Pro for easy downstream analysis after assembly.
  • Discover SNPs and small indels using Bayesian statistical models, identify large insertions and deletions, evaluate coverage, and annotate your consensus sequence.

ArrayStar

Gene Expression and SNP Analysis

  • Evaluate global gene expression experiments, compare sequence variation, analyze RNA-Seq, ChIP-Seq, CNV, miRNA, and more.
  • Analyze variants using assembly projects and/or SNP data from VCF files.
  • Utilize annotation data from dbSNP and other SNP and gene databases to enrich and filter variant data.
  • Import oligonucleotide microarray and spotted array data.
  • Isolate gene mutations of interest using graphically rich visualizations, and identify their biological significance.

GenVision Pro

Genomic Visualization Software

  • Visualize genomic sequencing results with high-quality, highly-customizable images that are easily exported for publication.
  • Browse and compare data sets for RNA-Seq, ChIP-Seq, CNV, exome and whole genome sequencing projects.
  • Compare coverage and peak plots to interpret gene expression and regulation.
  • Analyze mRNA isoforms and view coverage along exons in RNA-Seq data using Sashimi plots.

Genomics Suite includes the complete Molecular Biology Suite

The Genomics Suite includes all of the applications found below that are included in the Molecular Biology Suite.  Learn more about the Molecular Biology Suite or Molecular Biology Workflows.

SeqBuilder Pro Icon: Sequence Analysis, Cloning + Primer Design Software

SeqBuilder Pro

Cloning + Primer Design

MegAlign Pro Icon: Multiple Sequence Alignments

MegAlign Pro

Multiple Sequence Alignments 

SeqMan Pro Icon: Contig Assembly, Analysis + SNP Detection

SeqMan Pro

Contig Assembly, Analysis + SNP Detection

GeneQuest Icon: Gene Discovery + Gene Annotation

GeneQuest

Gene Discovery + Gene Annotation

MegAlign Icon: DNA + Protein Sequence Alignments + Analysis

MegAlign

DNA + Protein Sequence Alignments + Analysis

SeqNinja Icon: Automated Genome Sequence Editing

SeqNinja

Automated Genome Sequence Editing

PrimerSelect Icon: Advanced Prier Designer

PrimerSelect

Advanced Primer Designer

GenVision Icon: Annotated Genomes + Data Illustrations

GenVision

Annotated Genomes + Data Illustrations

EditSeq Icon: Importing + Editing Unusual Sequence File Types

EditSeq

Importing + Editing Unusual Sequence File Types

Virtual cloning is one of the workflows that can be done using the Molecular Biology Suite

Watch the overview of DNASTAR’s Genomics Suite

Genomics Suite PDF

Supporting all major next-gen sequencing workflows and technologies

RNA-Seq and ChIP-Seq Gene Expression Analysis

Genomics

• Reference guided genome and exome assemblies
• De novo genome assembly
• Targeted sequencing and gene panels
• Cancer genomics
• Metagenomics
• SNP detection accuracy >99%
• Copy number variation (CNV) calculation

Integrated Data Analysis and Visualization

• Visualization and analysis of genomic variation, gene expression and gene regulation data in a single project
• Genome-scale, multi-sample analysis and browsing for any project type
• Sanger sequencing validation of NGS assemblies and variant calls
• Viral-host integration analysis

Transcriptomics

• De novo transcriptome assembly with auto-mRNA annotation
• RNA-Seq gene expression analysis
• ChIP-Seq peak detection
• Microarray analysis
• miRNA discovery and quantification

Isoform Analysis for RNASeq

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  • Home
  • Product Updates
  • Software
    • Lasergene: Complete Suite
    • Molecular Biology Suite
    • Structural Biology Suite
    • Genomics Suite
    • Nova – Protein Modeling
    • DNASTAR Cloud
    • SeqBuilder Pro: Buy Online!
  • Workflows
    • Molecular Biology
    • Genomics + Transcriptomics
    • Protein Analysis + Structure Prediction
  • Resources
    • Product Notifications
    • Blog
    • Educational Software Request
    • Events
    • Documentation
    • Services
      • Grant Assistance
    • Technical Requirements
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  • Training
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    • Technical Support Request
  • About
    • Careers
    • Legal Information
    • Privacy Policy
    • Contact Us
  • Free Trial
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