Let Lasergene Genomics do the heavy lifting, so you can focus on the results.
As the availability of NGS technology has increased over the last decade, so have the tools for genomic data analysis. However, NGS data analysis often remains a challenge due to the sheer volume of data, the computing power needed, and the technical expertise required to prepare a project for assembly and analysis.
Lasergene Genomics stands apart in the field of genomic data analysis due in part to SeqMan NGen, our revolutionary wizard that enables you to set up your entire genomic sequencing project in mere minutes, and automates tasks that typically require extensive manual intervention in other commercially available NGS data analysis tools.
Our patented assembling algorithms enable you to assemble and align your genomic sequencing data with unsurpassed ease and speed, but should your project require more computing power, we provide integrated access to DNASTAR Cloud Assemblies, so that you can utilize our cloud computing resources to align and assemble your NGS data, and free up your local computer to do other things.
“This is the complete package, from assembly to analysis”
Never experienced a problem
“I have never experienced a problem with this easy to use package…I recommended it highly.”
Easy and fast
“It is easy and fast to identify SNPs, structural changes, and CNVs.”
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.”
Genomics Workflows FAQs
Which Lasergene package do I need for genomic data analysis?
Lasergene Genomics includes all the applications you need for our genomics and transcriptomics workflows. We also offer DNASTAR Lasergene, our complete software package which includes Lasergene Molecular Biology, Lasergene Protein, and Lasergene Genomics. We offer both academic and commercial pricing for convenient annual licenses, which include upgrades and unlimited access to our technical support team.
How do I access the genomics data analysis workflows in Lasergene?
Our genomic data analysis workflows can be accessed by clicking on the Genomics tab in DNASTAR Navigator.
What types of read technology are supported for genomic data analysis?
Lasergene Genomics supports Illumina, Oxford Nanopore, PacBio, 454, Sanger/ABI and Ion Torrent sequencing technologies. For a full list of supported file types, see our File Formats resource.
Can I try before I buy?
Yes! We offer free, no-obligation trials of our complete DNASTAR Lasergene package. We also understand that NGS data analysis can be complex and sometimes overwhelming. We get it! That’s why we offer free, one-on-one demonstrations, customized to your specific research objectives, and led by our scientists on staff.