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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
Analysis Software for All Major Next-Gen Sequencing Technologies
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
SeqBuilder Pro
MegAlign Pro
SeqMan Pro
GeneQuest
MegAlign
SeqNinja
PrimerSelect
GenVision
EditSeq
Watch the overview of DNASTAR’s Genomics Suite
Supporting all major next-gen sequencing workflows and technologies
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
