What solutions are available at MindWalk?

MindWalk information

- The MindWalk Retrieve and Relate application
- The MindWalk Variation Analysis: coming soon
- The MindWalk AI platform

MindWalk transformed the current methodology in omics analysis into an indexing problem, using HYFTSTM, structural anchor points in genetic code, With the MindWalk approach a wide variety of analyses on -omics data can be executed in one operation, at a lightning fast speed. Because we use exact matching, accuracy is unprecedented.

MindWalk’s transformational technology is the gateway to -omics data discoveries allowing for analysing petabytes of data, in sync with today’s data production. We greatly reduce the complexity of -omic data analysis and make analysis effective and available for a lot more researchers. So end users / researchers and users can say goodbye to errors, delays and frustration. Companies using our SaaS tools will be able to increase efficiency of their R&D departments and accelerate their development cycles.

Our patent-pending technology: Face Recognition Technology for genomics Smart applications – such as Face-Recognition Technology– recognize multiple features and translate them into a unique code representing one’s individual signature. This unique facial signature is then matched to other images. By introducing a FRT-like approach to -omics analysis we can recognize genetic or amino-acid sequences in an instance, detects patterns, and compare the reconstructed sequenced string with other - omics data to uncover similarities and differences between subjects and species in mere seconds.

The MindWalk Retrieve and Relate application 

With this tool you can compare, identify, relate and locate sequences. Searching for sequence similarities takes one mouse click and is executed simultaneously in RNA, DNA and proteins. Simply paste a biological sequence or certain functions, species or other metadata in the search bar to find similar sequences. Our revolutionary algorithm retrieves more relevant results than any other method. No need to set any preliminary parameters to restrict the search space. Multiple databases can be searched simultaneously. You can also add your own
data and filter your results in multiple granularities.

For more information visit our website

The MindWalk Variation Analysis: COMING SOON

We like to keep things simple and comprehensive. So, discover all kinds of variations (SNP’s, indels, structural variations…) across all domains with just one tool, less is more. We deliver the next level in accuracy, speed and flexibility. There are no limitations in the number of subjects or even species that can be compared.

Genomes can be added or left out of the equation with instant updating of results. These dynamic updates can be done without rebuilding the entire data-structure. Results can be clustered easily based on similarities and differences, which facilitates patient profiling and population studies and enhances developments in precision medicine. Large scale clustering makes variant identification less dependent on the reference genome or even surpasses the reference.

The MindWalk AI-platform

The accuracy of our variation analysis and our ability to detect structural anchor points (specific HYFTST TM or HYFTTM patterns related to disease, function...) is via AI techniques combined with all kinds of structured and unstructured data such as patient record data, scientific literature, data on protein structures and more. This enables us to identify very specific targets in patient subgroups or in crops of interest and optimises lead selection. Our AI toolbox enables identification of target areas for drug and biomarker development, assay design and gene therapy.

For more information, visit our website

For confidential consultation to discuss your research project requirements, schedule a meeting.