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Publications Citing Lasergene for Variant Detection and Analysis

07/28/2016 by Ellie Thomas
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  Did you know DNASTAR software has been cited in over 52,000 peer-reviewed publications? Every year for the past 31 years, our software has been cited in peer reviewed publications more than any competitor’s software.   Featured here are just … Continue reading →

Publications Citing Lasergene Molecular Biology Suite

07/28/2016 by Ellie Thomas
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  Did you know DNASTAR software has been cited in over 52,000 peer-reviewed publications? Every year for the past 31 years, our software has been cited in peer-reviewed journals more than any competitor’s software.   Featured here are just a few publications … Continue reading →

Publications Citing Lasergene for Bacterial Genome Assembly

05/24/2016 by Ellie Thomas
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Did you know DNASTAR software has been cited in over 52,000 peer-reviewed publications? Every year for the past 31 years, our software has been cited in peer reviewed publications more than any competitor’s software.   Featured here are some recent … Continue reading →

Lasergene Weekly: Got a minute? Check out Lasergene’s easy-to-use Gene Ontology workflow

05/17/2016 by Ellie Thomas
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Lasergene Genomics Suite makes it easy to integrate gene ontology data into your RNA-Seq, ChIP-Seq, microarray and variant analysis projects. See for yourself in our 60-second video, and check out the rest of our Quick Tips to see more Lasergene … Continue reading →

Lasergene Weekly: Join us for a Webinar on May 18th

05/10/2016 by Ellie Thomas
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  Webinar: Highly Accurate Protein Structure Prediction in NovaFold When: Wednesday, May 18th at 12:00 PM EDT   Would you like to hear from our experts about what’s new in NovaFold version 13? Want to get a first look at … Continue reading →

Lasergene Weekly: Have you tried Lasergene 13 yet?

05/03/2016 by Ellie Thomas
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  From molecular biology to genomics to structural biology, Lasergene 13 has something for everyone. This release is filled with new features and enhancements for easier research, and more accurate and comprehensive results. So what’s new in Lasergene 13? Visit … Continue reading →

Lasergene Weekly: 12 Studies Using Lasergene for Multiple Sequence Alignment

04/26/2016 by Ellie Thomas
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Did you know Lasergene is cited in peer reviewed publications more often than any other sequence analysis software? Check out our latest blog post to see highlights of 12 recent publications in which scientists use the Lasergene Molecular Biology Suite … Continue reading →

Publications Citing Lasergene for Multiple Sequence Alignment

04/25/2016 by Ellie Thomas
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Did you know DNASTAR software has been cited in over 52,000 peer-reviewed publications? Every year for the past 31 years, our software has been cited in peer reviewed publications more than any competitor’s software.   Featured here are some recent … Continue reading →

Lasergene Weekly: Join Us for a Webinar on April 27th

04/19/2016 by Ellie Thomas
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  Webinar: RNA-Seq for Non-Model Organisms When: Wednesday, April 27th at 12:00 PM EDT   Would you like to see how you can perform gene expression analysis for any organism, even without a reference genome? Join us for a webinar … Continue reading →

Lasergene Weekly: Predict a Protein in 3 Simple Steps

04/12/2016 by Ellie Thomas
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The Lasergene Structural Biology Suite allows you to run a protein structure prediction in just three steps. In 60 seconds, you can see how it’s done with this week’s Quick Tip video. Check out the rest of our Quick Tips … Continue reading →

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Follow Us:
  • WHAT'S NEW?
  • Software
    • DNASTAR Lasergene
    • Molecular Biology
    • Genomics
    • Structural Biology
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  • Contact Us
    • Company Profile
    • Careers
    • Distributors
    • Event Schedule
    • Legal Information
    • Press Releases
    • Privacy Statement
    • Download Free Trial
    • Request Educational Software
    • Request Quote
  • Molecular Biology
    • Cloning
    • Gene Discovery
    • Plasmid Auto-Annotation
    • Primer Design
    • Sanger Sequence Assembly
    • Sequence Alignment
  • Genomics
    • Automated Genome Closure
    • De Novo Genome Assembly
    • Genomic Visualization
    • Mendelian Gene Panels and Exome Analysis
    • Metagenomic Assembly with Host Removal
    • Reference Guided Genome Alignment
    • SNP Validation Control
    • Variant Analysis
  • Transcriptomics
    • ChIP-Seq Analysis
    • Combined Analysis for NGS Projects
    • De Novo Transcriptome Assembly
    • RNA-Seq Alignment
  • Clinical Research
    • Association Studies
    • Cancer Genomics
    • Gene Panels
    • Microarray Gene Expression Analysis
    • NGS Assembly with Sanger Validation
  • Structural Biology
    • Antibody Modeling
    • Epitope Prediction
    • Molecular Motion Visualization
    • Protein Docking
    • Protein Sequence & Structure
    • Protein Structure Prediction
    • Structural Alignment
  • NGS Support Materials
    • #1 in NGS Accuracy
    • Genome Template Packages
    • Benchmarks
    • Supported Sequencing Technologies
    • dbNSFP Gene Level Annotations
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