Products

SVCell™ provides advanced technology for the simple and intuitive recognition and quantitative analysis of data from microscopy images for a wide range of life science applications, through user directed learning without requiring image processing knowledge.

Image recognition, the definition and tracking of objects of interest in images, is the critical step in quantitative microscopy. However, existing image analysis software is difficult to use for image recognition, often requiring tedious manual drawing or the development of custom scripts. SVCell leverages SVision LLC’s advanced recognition and learning technologies to make the image recognition experience simple and intuitive for users. For the first time, scientists who use microscopy images in their experiments can count on a flexible, accurate and easy to use image recognition solution.

SVCell was launched on October 2006. SVCell’s development is partially funded by the National Institute of Health (NIH) under the Small Business Innovative Research (SBIR) program. Please visit us at www.svcell.com for more information.

Recognition Literature

Automated Kinetic Characterization of Exocytotic Events in Total Internal reflection microscopy New!

Automated Kinetic Characterization of Intracellular Single-molecule Tracking New!

Automatic quantitative characterization of kinetic events during exocytosis New!

Characterization of complex biological phenomena in time-lapse microscopy

Automatic receptor trafficking assay analysis using machine learning

Automatic Transfluor assay analysis using machine learning

Learnable tracking for multiple moving subcellular objects in time-lapse microscopy assays

Learnable analysis module for subcellular, time lapse microscopy assays

Robust tracking of multiple moving objects in subcellular time-lapse microscopy assays

Adaptive spatial-temporal detection of multiple moving objects in subcellular time-lapse assays

Automated Kinetic Analysis in Individual Cell Motility Assays

Automated Recognition and Tracking of Cells in Individual Cell Motility Assays

Spatial-temporal regulation improves the sensitivity and accuracy of synaptic vesicle recycling assays

Discovery framework for live cell synaptic vesicle recycling assays

Robust modeling for the automated analysis of synaptic vesicle recycling assays

Homologous chromosomes associate during hematopoiesis

Robust analysis of subcellular, time-lapse microscopy assays