smarts.bio

smarts.bio brings your bioinformatics workspace to your phone and tablet. Ask a question in plain English and get an answer grounded in your own data, then open the file, run the analysis, and check the result without going back to a terminal. WHAT YOU CAN DO • Ask anything about your data. Describe what you want in ordinary language and let the agent pick the tools, run them, and explain what came back. • Open your files properly. Built-in viewers for sequences (FASTA, FASTQ), alignments (SAM, BAM, CRAM), variants (VCF, BCF), structures (PDB, mmCIF) and tables (CSV, TSV), with real rendering, not a text dump. • Analyse what you're looking at. GC content, ORFs and restriction sites for DNA; mapping rate, MAPQ and insert-size distributions for alignments; Ts/Tv ratio and FILTER pass rates for variants; chains, resolution and secondary structure for models; descriptive statistics, correlation and group comparisons for tables. • Photograph a plate. Capture an image from the bench and get colony counts, band detection or cell counts back, with the photo saved to your workspace. • Search the literature and databases. One query across gene, protein, variant, pathway and publication sources, with results you can open or hand to the agent. • Run and watch pipelines. Start quality control, alignment or RNA-seq runs and follow their progress, with logs and the option to cancel. • Keep everything in one workspace. Upload, rename, move and organise files; edit and save them in place; everything you do here is the same workspace you use elsewhere. BUILT FOR PEOPLE AT THE BENCH Most bioinformatics tooling assumes you're sitting at a workstation. This is for the hours you're not, reading a result between experiments, checking whether a run finished, photographing a plate while your hands are still gloved. smarts.bio is a research tool. It is not a medical device and is not intended for diagnosis or treatment.