Accelerate your synthetic biology research with a comprehensive, automated toolkit designed for precision—from DNA design to sequence alignments and beyond.
Create and export clear, visual representations of genetic designs for use in presentations, papers, and reports.
Customizable Genetic Schematics
Easily draw and visualize genetic designs using a variety of colors and symbols to represent DNA parts, ensuring your designs are clear and easy to understand.
Export Real Designs to Schematics
Convert your actual genetic designs into detailed schematics with just a few clicks, allowing you to create professional visuals that can be used for academic papers, presentations, and documentation.
Flexible Export Options Export your schematics as high-quality images for seamless integration into your research publications or reports, ensuring clear communication of your designs.
Reduce Human Error
Control every aspect of your combinatorial designs with advanced rule-setting capabilities.
Dynamic Ruleset Creation
Easily define validation logic to constrain and guide your designs. For example, tag parts with specifications like “backbone” or “CDS,” and apply base pair-level rules such as ensuring all coding sequences begin with “ATG.”
Enhanced Validation
Automatically validate each design as you work, ensuring parts align with your project specifications and reducing the risk of errors in assembly and production.
“Automated biological design is an essential foundation for our carbon recycling technology and TeselaGen has a reliable platform for modern industrial DNA design and cloning.”
Dr. Michael Köpke
Vice President Synthetic Biology, LanzaTech
Sequence Alignment
Align, analyze, and visualize sequences with a suite of powerful bioinformatics tools.
Pairwise and Multiple Sequence Alignment
Run pairwise alignments for comparing sequence pairs or use multiple sequence alignments to identify homologous regions across different sequences, enhancing your comparative studies.
Advanced NGS Reads Mapping Efficiently map short NGS reads to long reference sequences, simplifying variant calling and identification of mutations.
Sanger Sequencing & Chromatogram Visualization Visualize sequencing chromatograms for accurate interpretation of Sanger sequencing data, ensuring that you can confidently confirm sequence accuracy.
DAPPER Tool for Parallel Part Alignments
Align parallel parts to expose regions of diversity, aiding in the identification of critical areas for sequence optimization or protein engineering.
Push the boundaries of science. We'll handle the rest.
Our team at TeselaGen shares your passion for biotech innovation. With extensive expertise in biotech R&D, we collaborate with you to bring your vision to life, ensuring that every step of your journey is backed by unparalleled support.
Are you an academic group? A startup? An enterprise?
Don’t worry, we have something for everyone. Schedule a demo today.