• Software
    • DNASTAR LASERGENE
      Comprehensive Sequence Analysis
      • Lasergene Molecular Biology
      • Lasergene Genomics
      • Lasergene Protein
    • NOVA APPLICATIONS
      Protein Modeling
      • NovaFold AI
      • NovaFold
      • NovaFold Antibody
      • NovaDock
  • Workflows
    • Molecular Biology Workflows
      • Automated Virtual Cloning
      • Clone Sequence Verification
      • Gel Electrophoresis Simulation
      • Multiple Sequence Alignment
      • Pairwise Sequence Alignment
      • PCR Site-Directed Mutagenesis
      • PCR Primer Design
      • Phylogenetic Analysis
      • Plasmid Maps
      • Sanger Sequence Assembly
      • Sequence Editing and Annotation
  • Protein Analysis
    • Antibody Modeling
    • Antibody Phage Display
    • Epitope Prediction
    • Protein Docking
    • Protein Sequence Analysis
    • Protein Stability Prediction
    • Protein Structural Alignment
    • Protein Structure Analysis
    • Protein Structure Prediction
  • Genomics
    • Clinical Research
    • De Novo Genome Assembly
    • Mauve Genome Alignment
    • Metagenomic Assembly
    • Variant Analysis
    • Viral Genome Analysis
    • Whole Genome/Whole Exome
  • Transcriptomics
    • ChIP-Seq Data Analysis
    • De Novo Transcriptome Assembly
    • RNA-Seq Alignment
  • Services
    • Protein Services
    • Genomic Services
  • Pricing
  • Resources
    • Product Updates
    • Product Notifications
    • Blog
    • Educational Software Request
    • Documentation
    • Technical Requirements
      • File Formats
      • Licensing Options
  • Training
    • Help + Tutorials
    • Webinars
    • Technical Support Request
  • About
    • Careers
    • Distributors
    • Legal Information
    • Privacy Policy
  • Contact

QUESTIONS? CALL 866.511.5090

DOWNLOAD FREE TRIAL
SHOPPING CART
MY ACCOUNT
DNASTAR DNASTAR
  • Software
    • DNASTAR LASERGENE
      Comprehensive Sequence Analysis
      • Lasergene Molecular Biology
      • Lasergene Genomics
      • Lasergene Protein
    • NOVA APPLICATIONS
      Protein Modeling
      • NovaFold AI
      • NovaFold
      • NovaFold Antibody
      • NovaDock
  • Workflows
    • Molecular Biology
      • Automated Virtual Cloning
      • Clone Sequence Verification
      • Gel Electrophoresis Simulation
      • Multiple Sequence Alignment
      • Pairwise Sequence Alignment
      • PCR Site-Directed Mutagenesis
      • PCR Primer Design
      • Phylogenetic Analysis
      • Plasmid Maps
      • Sanger Sequence Assembly
      • Sequence Editing and Annotation
    • Protein Analysis
      • Antibody Modeling
      • Antibody Phage Display
      • Epitope Prediction
      • Protein Docking
      • Protein Sequence Analysis
      • Protein Stability Prediction
      • Protein Structural Alignment
      • Protein Structure Analysis
      • Protein Structure Prediction
    • Genomics
      • Clinical Research
      • De Novo Genome Assembly
      • Mauve Genome Alignment
      • Metagenomic Assembly
      • Variant Analysis
      • Viral Genome Analysis
      • Whole Exome/Genome Sequencing
    • Transcriptomics
      • ChIP-Seq Data Analysis
      • De Novo Transcriptome Assembly
      • RNA-Seq Alignment and Analysis
  • Services
    • Protein Services
    • Genomic Services
  • Pricing
  • Resources
    • Product Updates
    • Product Notifications
    • Blog
    • Educational Software Request
    • Documentation
    • Technical Requirements
      • File Formats
      • Licensing Options
  • Training
    • Help + Tutorials
    • Webinars
    • Technical Support Request
  • About
    • Careers
    • Distributors
    • Legal Information
    • Privacy Policy
  • Contact

DNASTAR Resources


Category Archive for "Clinical Research"

Rapid, Large-Scale Prioritizing of Human Variants with Lasergene Genomics Suite

Rapid, Large-Scale Prioritizing of Human Variants with Lasergene Genomics Suite

Sep 7, 2016

Lasergene Genomics Suite now includes access to the Variant Annotation Database (VAD) for human sequencing...

DNASTAR LabViews: Blaire Bacher of Orion Genomics

DNASTAR LabViews: Blaire Bacher of Orion Genomics

Jun 21, 2016

In this installment of DNASTAR LabViews, we talk with Blaire Bacher of Orion Genomics about her work sequencing...

Dr. Michael Pauly of Mapp Biopharmaceutical on Ebola and ZMapp

Dr. Michael Pauly of Mapp Biopharmaceutical on Ebola and ZMapp

Oct 7, 2015

The Ebola epidemic in West Africa has proven to be a devastating reminder that humans...

How Accurate Is Your Variant Caller?

How Accurate Is Your Variant Caller?

Sep 23, 2015
Discovery of Gene Candidates from NGS Data Using A Researcher Friendly Pipeline and Filters

Discovery of Gene Candidates from NGS Data Using A Researcher Friendly Pipeline and Filters

Nov 20, 2014

In the past decade, the ability to determine complex mechanisms underlying disease has been made...

Q&A With Dr. Sheldon Garrison of Promentis Pharmaceuticals

Q&A With Dr. Sheldon Garrison of Promentis Pharmaceuticals

Nov 14, 2014

We chatted with Dr. Sheldon Garrison, Director of Pediatric and Rare Diseases at Promentis Pharmaceuticals...

GIAB Use Case:  Bringing NA12878 Call Sets to Kidney Disease

GIAB Use Case: Bringing NA12878 Call Sets to Kidney Disease

Oct 7, 2014

Nephropath™ incorporates DNASTAR pipeline for validating processes against NIST “gold standard.” The resources provided by...

Q&A with Dr. Luke Daum of Longhorn Vaccines and Diagnostics

Q&A with Dr. Luke Daum of Longhorn Vaccines and Diagnostics

Sep 25, 2014

We chatted with Dr. Luke Daum, Chief Scientific Officer at Longhorn Vaccines and Diagnostics about...

Search Blog Posts

Categories

  • Best Practices
  • Clinical Research
  • DNASTAR Customer Stories
  • DNASTAR News
  • Events
  • Long Read Sequencing
  • Molecular Biology
  • Newsletters
  • Next-Gen Sequencing
  • Press Releases
  • Product Notifications
  • Product Updates
  • Publications
  • Resources
  • Structural Biology
  • Webinars
  • Workflows

Recent Posts

  • Lasergene 17.3.3 Release Notes June 29, 2022
  • Streamlining Variant Identification and Analysis Webinar June 23, 2022
  • Variant Annotation with Lasergene Genomics: The easy way to discover, annotate and filter sequence variants June 10, 2022
  • Expert-Guided Protein Structure Prediction Webinar May 13, 2022
  • Lasergene 17.3.2 Release Notes May 9, 2022

Tags

assembling sequences cloud Cloud Assemblies customers De Novo Assembly DNASTAR Genomics Lasergene Metagenomics Metagenomic Sequencing NCBI GenBank newsletters next-gen NGS NGS Sequence Alignment NGS Sequence Asembly publications seqbuilder pro SeqMan NGen sequence assembly Webinar

Archives

Find us on

Most Commented Posts

  • Lasergene 15.3 Release Notes By Katie Maxfield on October 24, 2018 4
  • EditSeq, PrimerSelect and classic MegAlign retired with the release of Lasergene 16.0 By Sharon Yildiz on July 12, 2019 4
  • How much disk space do I need for my templated genome assembly? By DNA STAR on November 24, 2015 4

Would you like to receive technical tips and special offers straight to your inbox?

  • Pricing
  • Software
  • Workflows
  • Resources
  • Training
  • About

Get a 14-Day free trial of our complete Lasergene package. Try before you buy!

FREE TRIAL DOWNLOAD

© 2022 — DNASTAR Privacy Policy

This website uses cookies to improve user experience and understand our web usage. By continuing to use our website, you consent to our use of cookies. Accept
Privacy & Cookies Policy
Necessary
Always Enabled