Sequencing
Sequencing pipelines
QC, alignment, variant calling and expression analysis, from FASTQ to a report, as versioned and reproducible pipelines.
In silico research tools
Bioinformatics pipelines and analysis apps designed around your data and your questions. Built by a scientist, tested like software, and handed over so your team can run them.
What we build
Every tool is built for one team's data, questions and infrastructure, and every one ends in something a bench scientist can use.
Sequencing
QC, alignment, variant calling and expression analysis, from FASTQ to a report, as versioned and reproducible pipelines.
Microbiology
Assembly, annotation, strain typing and phylogenies, and screening for resistance and virulence genes across your isolates.
Structure
Structure prediction with AlphaFold 2, ESMFold or other models licensed for commercial use, docking and virtual screening, and sequence-to-structure analysis at scale.
Design
Primers and probes, CRISPR guides, codon optimization and in silico cloning, with your lab's rules built in.
Analysis
Dose-response and growth-curve fitting, qPCR quantification, and models trained on your own assay data.
Interfaces
Web interfaces around all of the above, so nobody needs a terminal, a cluster account or a bioinformatician to run an analysis.
Try it
Paste a DNA sequence, or use the EGFP coding sequence below, and get the first things a bench scientist checks. Nothing is uploaded: every calculation runs on your device.
Open reading frames, all six frames
Frame +1, 1..720, 720 nt, 239 aa. 1 ORF of at least 50 aa in total.
Longest ORF, translated
MVSKGEELFTGVVPILVELDGDVNGHKFSVSGEGEGDATYGKLTLKFICTTGKLPVPWPTLVTTLTYGVQCFSRYPDHMKQHDFFKSAMPEGYVQERTIFFKDDGNYKTRAEVKFEGDTLVNRIELKGIDFKEDGNILGHKLEYNYNSHNVYIMADKQKNGIKVNFKIRHNIEDGSVQLADHYQQNTPIGDGPVLLPDNHYLSTQSALSKDPNEKRDHMVLLEFVTAAGITLGMDELYK
TTACTTGTACAGCTCGTCCATGCCGAGAGTGATCCCGGCGGCGGTCACGAACTCCAGCAGGACCATGTGATCGCGCTTCTCGTTGGGGTCTTTGCTCAGGGCGGACTGGGTGCTCAGGTAGTGGTTGTCGGGCAGCAGCACGGGGCCGTCGCCGATGGGGGTGTTCTGCTGGTAGTGGTCGGCGAGCTGCACGCTGCCGTCCTCGATGTTGTGGCGGATCTTGAAGTTCACCTTGATGCCGTTCTTCTGCTTGTCGGCCATGATATAGACGTTGTGGCTGTTGTAGTTGTACTCCAGCTTGTGCCCCAGGATGTTGCCGTCCTCCTTGAAGTCGATGCCCTTCAGCTCGATGCGGTTCACCAGGGTGTCGCCCTCGAACTTCACCTCGGCGCGGGTCTTGTAGTTGCCGTCGTCCTTGAAGAAGATGGTGCGCTCCTGGACGTAGCCTTCGGGCATGGCGGACTTGAAGAAGTCGTGCTGCTTCATGTGGTCGGGGTAGCGGCTGAAGCACTGCACGCCGTAGGTCAGGGTGGTCACGAGGGTGGGCCAGGGCACGGGCAGCTTGCCGGTGGTGCAGATGAACTTCAGGGTCAGCTTGCCGTAGGTGGCATCGCCCTCGCCCTCGCCGGACACGCTGAACTTGTGGCCGTTTACGTCGCCGTCCAGCTCGACCAGGATGGGCACCACCCCGGTGAACAGCTCCTCGCCCTTGCTCACCAT
MVSKGEELFTGVVPILVELDGDVNGHKFSVSGEGEGDATYGKLTLKFICTTGKLPVPWPTLVTTLTYGVQCFSRYPDHMKQHDFFKSAMPEGYVQERTIFFKDDGNYKTRAEVKFEGDTLVNRIELKGIDFKEDGNILGHKLEYNYNSHNVYIMADKQKNGIKVNFKIRHNIEDGSVQLADHYQQNTPIGDGPVLLPDNHYLSTQSALSKDPNEKRDHMVLLEFVTAAGITLGMDELYK*
Standard genetic code (NCBI table 1). An ORF starts at ATG and ends at the first in-frame stop codon; positions are 1-based on the sequence as entered, and minus-strand ORFs are shown as complement(start..end). A demo, not a validated tool: the pipelines we build for you are tested against data with known answers.
Microbial genomics
A microbiologist knows which question the genome has to answer: which strains are related, what they carry, and whether the lab should worry.
Results you can defend
Pipelines are versioned, containerized and pinned, so the same input gives the same result next year.
Before you rely on a pipeline, it runs on data where the answer is known, and the comparison is in the handover.
Every release comes with the versions, parameters and references you need for a report, a paper or an audit.
Your cloud account, your cluster or your own servers. Large files stay put; the pipeline goes to them.
Next step
Tell us in a 30-minute call. You'll leave with a clear next step, whether or not we end up working together.