LASERGENE GENOMICS

Comprehensive NGS software for genomics, transcriptomics and clinical research.

Lasergene Genomics

Lasergene Genomics has established a new standard in the fields of genomics and transcriptomics. Powered by SeqMan NGen, our revolutionary and user-friendly assembler, Lasergene Genomics enables you to set up complex genomic sequencing projects in just minutes. It also automates tasks that typically require extensive manual intervention in other software packages.

Beyond intuitive project setup, Lasergene Genomics provides powerful analysis tools, including GenVision Pro, an advanced genome browser designed for visualizing and analyzing genomic data across multiple samples. Our integrated solution offers efficiency and clarity – you can seamlessly assemble sequences, identify critical variants, and determine differentially expressed genes – all in one place.

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Lasergene Genomics Workflows

ChIP-Seq Data Analysis

Clinical Research

De Novo Genome Assembly

De Novo Transcriptome Assembly

Metagenomic Assembly

RNA-Seq Alignment and Analysis

Variant Analysis

Viral Genome Analysis

Whole Exome/Whole Genome Sequencing

Lasergene Genomics Applications

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.

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

Powerful Genomic Visualization and Analysis

Visualize and analyze genomic data across multiple samples, effortlessly filter and compare variants, and generate stunning, customizable images for publication.

ArrayStar

Gene Expression and Gene Ontology

ArrayStar’s advanced filtering tools and rich visualizations enable you to easily evaluate gene expression and gene ontology for RNA-Seq and ChIP-Seq data sets.

Lasergene Genomics Benchmarks

Faster NGS Analysis Workflows

Lasergene 19 delivers improved performance across genome assembly and variant analysis workflows, helping researchers process sequencing datasets more efficiently. Performance optimizations across multiple sequencing technologies reduce runtime for both routine and large-scale projects, enabling faster turnaround from raw sequencing data to downstream interpretation and analysis. Benchmark testing demonstrated reduced analysis times across a range of dataset sizes, including complex plant and human genomes.

Faster performance across PacBio HiFi, ONT duplex, and Illumina datasets
Reduced runtime for large and complex sequencing projects
Improved efficiency across diverse genome sizes and dataset scales
Enhanced performance for modern long-read sequencing datasets

Resources

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

Lasergene Genomics Overview

View Document

Maximizing Insights from Multi-Sample Variant Analysis

Watch Webinar

7 Steps for Human Variant Analysis

Download eBook

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, GenVision Pro, and ArrayStar, as well as access to 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 Lasergene Genomics technical requirements for details.

Because performing…

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

How much does Lasergene Genomics cost?

We offer both academic and commercial pricing for convenient annual licenses of Lasergene Genomics, which include upgrades and 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

	Lasergene Molecular Biology	Lasergene Genomics	Lasergene Protein	MOST POPULARDNASTAR Lasergene
				MOST POPULARDNASTAR Lasergene
Included Applications
SeqBuilder Pro
SeqMan Ultra
MegAlign Pro
GeneQuest
GenVision
SeqNinja
SeqMan NGen
ArrayStar
GenVision Pro
Protean 3D
DNASTAR Navigator
Supported Workflows
Antibody Phage Display
Automated Virtual Cloning
Clone Sequence Verification
ELN Integration
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
Viral Genome Analysis
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
NovaCloud
NovaLocal
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