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LASERGENE GENOMICS

Comprehensive NGS software for genomics, transcriptomics and clinical research.

Home » DNASTAR Bioinformatics Software » DNASTAR Lasergene » Lasergene Genomics

Lasergene Genomics

Lasergene Genomics stands apart in the fields of genomics and transcriptomics. Powered by SeqMan NGen, our revolutionary and easy-to-use assembler, the software enables you to set up complex genomic sequencing projects in mere minutes, and automates tasks that typically require extensive manual intervention in other software packages.

Intuitive project setup and analysis, combined with our patented assembly algorithms, allow you to assemble and align your NGS data with unsurpassed ease and speed, so that you can focus on the results. No more switching between software tools to assemble sequences, identify important variants, and determine differentially expressed genes. Everything you need is here.

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Learn more about Lasergene Genomics

Workflows   | Applications   | Resources   | FAQs   | Compare Packages

Lasergene Genomics Workflows

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ChIP-Seq Data Analysis

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Clinical Research

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De Novo Genome Assembly

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De Novo Transcriptome Assembly

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Metagenomic Assembly

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RNA-Seq Alignment and Analysis

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Variant Analysis

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Whole Exome/Whole Genome Sequencing

Lasergene Genomics Applications

SeqMan NGen

SeqMan NGen

Genomic Sequence Assembly

SeqMan NGen enables you to set up complex genomic sequencing projects in mere minutes, then assembles NGS and long read sequencing data with unsurpassed ease and speed.

ArrayStar Venn Diagram

ArrayStar

Gene Expression and Variant Analysis

ArrayStar’s advanced filtering tools and rich visualizations enable you to easily evaluate gene expression, and identify significant variants across multiple samples.

SeqMan Ultra

SeqMan Ultra

Sequence Assembly Analysis and Editing

SeqMan Ultra provides post-assembly analysis tools, such as evaluating coverage, analyzing variants within the context of the alignment, and contig editing.

GenVision Pro

GenVision Pro

Genomic Visualization Software

Visualize genomic sequencing results such as coverage and peak plots using highly-customizable images that are easily exported for collaboration or publication.

DNASTAR Cloud Assemblies

DNASTAR Cloud*

Cloud-Based Storage and Assemblies

DNASTAR Cloud Data Drive provides NGS data management. DNASTAR Cloud Assemblies* utilizes our cloud computing resources to align and assemble your NGS data, freeing up your local computer to do other things.

*Each Lasergene Genomics license includes 5 free DNASTAR Cloud Assemblies. Further cloud assemblies require an additional purchase.

Resources

Please see our resources below for more information on Lasergene Genomics.

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Lasergene Genomics Overview

View Document

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How to Assemble Genomes like a Bioinformatics Pro

Read Blog Post

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Choosing the best assembly strategy for your genomic sequencing data

Watch Webinar

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RNA-Seq Assembly and Normalization Methods—an Interview with Dr. Carl-Erik Tornqvist

Read Blog Post

  • One of the best

    “It is a very powerful application; A run can be assembled with a reference genome in few minutes. SeqMan NGen is one of the best software applications of DNASTAR.”

    Elisabeth Navarro, CNRS

  • Easy and fast

    “It is easy and fast to identify SNPs, structural changes, and CNVs.”

    Kirk Nelson, Qpex Biopharma Inc.

  • Never experienced a problem

    “I have never experienced a problem with this easy to use package…I recommended it highly.”

    Dr. Andrew M. Kropinski, University of Guelph

  • Complete package

    “This is the complete package, from assembly to analysis”

    Marjorie Beggs, Arkana Laboratories

FAQs

What types of genome analysis can I do with Lasergene Genomics?

Lasergene Genomics includes all the applications you need for clinical research studies, de novo genome assembly, metagenomic assembly, advanced variant analysis, whole exome/genome sequencing, and transcriptomics studies such as ChIP-Seq, RNA-Seq, and de novo transcriptome assemblies.

Which applications are included with a Lasergene Genomics license?

Lasergene Genomics includes SeqMan NGen, SeqMan Ultra, ArrayStar, GenVision Pro, as well as five (5) DNASTAR Cloud Assemblies.

Do I need a powerful computer to run Lasergene Genomics?

Not necessarily. To run Lasergene Genomics locally, hardware requirements vary based on the type of projects you plan to do. Please see our technical requirements for details.

Because performing large scale NGS alignments or de novo sequence assemblies can require significant hard disk space and memory, we offer DNASTAR Cloud Assemblies, so that you can easily utilize our cloud computing resources to align and assemble your NGS data, using any laptop or desktop computer that meets our minimum technical requirements.

Every free trial and purchase of Lasergene Genomics includes 5 free DNASTAR Cloud Assemblies.

How much does Lasergene Genomics cost?

We offer both academic and commercial pricing for convenient annual licenses of Lasergene Genomics, which include upgrades and unlimited access to our technical support team.

We also offer floating licenses for networks, and site licenses that can be shared with an entire organization. For pricing on network or site licenses, please request a quote.

Can I try Lasergene Genomics before I buy it?

Yes! We offer free, no-obligation trials of our complete DNASTAR Lasergene package.

Because genomics projects can be complex and sometimes overwhelming, we also encourage you to sign up for a free, one-on-one demonstration, customized to your specific research objectives and led by one of the scientists on staff.

Compare DNASTAR Lasergene Packages

 MOST POPULARDNASTAR Lasergene
Lasergene Molecular BiologyLasergene GenomicsLasergene Protein
Included Applications
SeqBuilder Pro
SeqMan Ultra
MegAlign Pro
GeneQuest
GenVision
SeqNinja
SeqMan NGen
ArrayStar
GenVision Pro
Protean 3D
(+1 prediction per Nova Application)
DNASTAR Navigator
Supported Workflows
Automated Virtual Cloning
Clone Sequence Verification
Gel Electrophoresis Simulation
Mauve Genome Alignment
Multiple Sequence Alignment
Pairwise Sequence Alignment
PCR Primer Design
PCR Site-Directed Mutagenesis
Phylogenetic Analysis
Plasmid Maps
Sequence Editing and Annotation
Sanger Sequence Assembly
ChIP-Seq Data Analysis
Clinical Research
De Novo Transcriptome Assembly
Large Scale Variant Analysis
Metagenomic Assembly
NGS De Novo Genome Assembly
RNA-Seq Alignment
Whole Exome/Genome Sequencing
Antibody Modeling
Epitope Prediction
Protein Docking
Protein Sequence Analysis
Protein Stability Prediction
Protein Structural Alignment
Protein Structure Analysis
Protein Structure Prediction
Integrates with
DNASTAR Cloud Data Drive
DNASTAR Cloud Assemblies  
NovaDock
NovaFold
NovaFold Antibody
Pricing
Annual pricing starting at:

$599/year
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$1,499/year
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$799/year
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$2,399/year
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