Sanger Sequencing Analysis
Improve your mapping accuracy and decrease your analysis time with simple sequence assembly and easy editing of contigs.
Easily identify, examine and resolve disagreements with powerful SNP detection and variant calling.
Next Generation Sequencing Analysis
Beautiful visualizations of annotated genomes and assemblies displayed in a highly customizable sequence view.
Powerful SNP variants analysis, simple RNA-Seq expression analysis and amplicon metagenomics.
NGS Pre-Processing, Assembly and Mapping
Ensure accurate downstream analysis with extensive NGS pre-processing tools producing clean sequence data.
Reliable reference mapping for short or long reads with exclusive mapping algorithms and flexible de novo genome assembly.
Alignment
Perform pairwise and multiple alignments of DNA or protein using trusted algorithms, including MAFFT and Clustal Omega.
Phylogenetics
Build phylogenetic trees using peer-reviewed algorithms, including RAxML and PAUP*, and adjust display settings.
Cloning
Simulate low and high throughput cloning experiments including Golden Gate, Gateway, Gibson, Restriction and Parts Cloning.
Validate your cloning with a visual tool for automating sequence alignment during batch plasmid validation.
Primer Design
Design and test PCR and sequencing primers, and create your own searchable primer database.
Be confident your primers will only bind in a single location with automatic identification of any additional, off target, binding sites.
CRISPR
Powerful CRISPR tools make it easy to find specific sites, design guide RNAs and analyze your editing results.