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GENEQUEST

Locate and annotate genes, regulatory elements, and other regions of interest on your DNA sequence.

GeneQuest

Finding and annotating the genes and regulatory elements on a sequence can often prove to be a challenge without a centralized tool for evaluating multiple analysis methods.  GeneQuest’s comprehensive set of analytical methods facilitate gene discovery and gene annotation by identifying ORFs, predicting coding regions, and analyzing the structure and composition of your sequence, all on a centralized assay surface. GeneQuest locates repetitive portions of your sequence and lets you display restriction sites and features, plot base frequency and base skew, and predict RNA folding and localized DNA bending, enabling you to easily identify and annotate genes.

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GeneQuest

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Resources

Please see our resources below for more information on the gene discovery and gene annotation tools in GeneQuest.

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Getting Started with GeneQuest

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GeneQuest Help

User Guide

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GeneQuest Tutorials

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FAQs

Which Lasergene package includes GeneQuest?

GeneQuest is included in Lasergene Molecular Biology as well as in the complete DNASTAR Lasergene package which includes all of the applications from Lasergene Molecular Biology, Lasergene Protein, and Lasergene Genomics.

What file types can I import into GeneQuest?

In addition to supporting output from most Lasergene applications, GeneQuest also accepts ABI, DNA Multi-Seq, FASTA, GenBank, Phred, RNA Fold files, .scf, .fof, and .zip files.

How can I export a publication-quality image of my annotated sequence from GeneQuest?

GeneQuest works in conjunction with GenVision to produce publication-quality images of your annotated sequences. Export your project in GenVision format by selecting File>Export as GenVision Project.

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
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
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