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  • PCR Primer Design
  • Sanger Sequence Assembly
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  • Protein Docking
  • Protein Structure Prediction
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SEQMAN ULTRA

Accurately trim, assemble, evaluate, and edit Sanger and NGS sequencing data.

Home > DNASTAR Bioinformatics Software > DNASTAR Lasergene > SeqMan Ultra

SeqMan Ultra

SeqMan Ultra is the new face of SeqMan Pro, our longstanding sequence assembly software application, complete with a new modern, intuitive interface, as well as lots of performance improvements under the hood. SeqMan Ultra uses the most accurate contig assembly algorithm for Sanger sequence assemblies, and provides extensive post-assembly analysis tools for both Sanger and NGS assemblies. When compared to the competition, our algorithm does the best job assembling Sanger sequences into a single contig, and calling the most accurate consensus sequence based on trace quality and shape. Following assembly, SeqMan Ultra uniquely offers you the ability to easily edit your assembled data – exposing or trimming ends, introducing mutations – as well as analyzing your assembled data, including viewing chromatograms, evaluating coverage, analyzing variants, and examining multiple samples organized within a single contig.

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Learn more about SeqMan Ultra

Workflows   | Resources   | FAQs   | Compare Packages

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SeqMan Ultra-Related Workflows

Sanger Sequence Assembly

Clinical Research

De Novo Genome Assembly

Metagenomic Assembly

Variant Analysis

Viral Genome Analysis

Whole Genome/Exome Sequencing

Resources

Please see our resources below for more information on SeqMan Ultra.

What’s New in SeqMan Ultra 17.2?

Watch Webinar

Get to Know SeqMan Ultra Webinar

Watch Webinar

Transitioning from SeqMan Pro to SeqMan Ultra Webinar

Watch Webinar

Dr. Michael Pauly of Mapp Biopharmaceutical on Ebola and ZMapp

Read Blog Post

Sanger Sequence Assembly in SeqMan Ultra

Watch Video

SeqMan Ultra Help

User Guide

SeqMan Ultra Tutorials

Tutorials

FAQs

What’s the difference between SeqMan NGen, SeqMan Ultra, and SeqMan Pro?

SeqMan NGen and SeqMan Ultra are two applications that work together to assemble and analyze both Sanger and NGS sequencing data. SeqMan NGen is the application that assembles and aligns the data, and is fully integrated in SeqMan Ultra so that you can go from streamlined project setup to finished assembly all in one application. SeqMan Ultra is one of the sequence assembly tools that allows you to analyze and edit the assembly produced by SeqMan NGen. (Additional applications within Lasergene Genomics are available for analyzing NGS projects and more complex Sanger assemblies).

SeqMan Ultra is the new face of SeqMan Pro, our longstanding contig assembly software application, complete with a new modern, intuitive interface, as well as lots of performance improvements under the hood. SeqMan Ultra is a 64-bit application, which means when compared to the 32-bit SeqMan Pro application, it offers faster project opening, better performance for analyzing large files, increased capacity, and compatibility with macOS 10.15. SeqMan Pro will still be available in Lasergene 17, but will eventually be completely replaced by SeqMan Ultra.

Which Lasergene package includes SeqMan Ultra?

SeqMan Ultra is included with Lasergene Molecular Biology, Lasergene Genomics, and the complete DNASTAR Lasergene package.

With a Lasergene Molecular Biology license, SeqMan Ultra is available for Sanger sequence assemblies only.

With a Lasergene Genomics or DNASTAR Lasergene license, SeqMan Ultra is available for all NGS assemblies as well as Sanger sequence assemblies.

Can I edit my assembled sequences in SeqMan Ultra?

Yes. An assembly run in SeqMan Ultra or SeqMan NGen produces a fully editable project which can be edited at base-level and contig-level in SeqMan Ultra.

Compare DNASTAR Lasergene Packages

  MOST POPULARDNASTAR Lasergene
Lasergene Molecular Biology Lasergene Genomics Lasergene 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
Antibody Phage Display
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
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  
NovaDock
NovaFold
NovaFold Antibody
Pricing
Annual pricing starting at:

$699/year
See Pricing

$1,579/year
See Pricing

$799/year
See Pricing

$2,519/year
See Pricing
   

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