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Undefined Software Near USA
16,621 software items found
by:Aiforia Technologies  based inCambridge, MASSACHUSETTS (USA)
Creates a heatmap assisting the pathologist in automatically finding the critical areas of the sample. Rapidly distinguishes between normal and cancerous tissue supporting the pathologist in the quick detection of tumor epithelium. Automatically scores the ER positive and negative cells of epithelial origin from either WSI or selected image areas, saving the pathologist time. Provides intelligent ...
by:Aiforia Technologies  based inCambridge, MASSACHUSETTS (USA)
Rapidly distinguishes between normal and cancerous tissue supporting the pathologist in the quick detection of tumor areas. Automatically scores a quantitative Gleason grade score and grade group from WSI, saving the pathologist time. Provides visual feedback as it allows to view images in different magnifications, move in different x-y-z-locations, view image analysis results, and mark and ...
by:Aiforia Technologies  based inCambridge, MASSACHUSETTS (USA)
Creates a heatmap assisting the pathologist in automatically finding the critical areas of the sample. Rapidly distinguishes between normal and cancerous tissue supporting the pathologist in the quick detection of tumor epithelium. Automatically scores the PD-L1 positive and negative cells of epithelial origin from whole slide images (WSI) saving the pathologist time when evaluating patient ...
by:Aiforia Technologies  based inCambridge, MASSACHUSETTS (USA)
Rapidly displays AI-assisted analysis results in an intuitive and easily readable format and enabling case prioritization based on severity. Automatically generates reports from analyses by clinical AI models, significantly saving the pathologist time and improving the lab’s overall output efficiency. Supports full interaction with the pathologist by allowing viewing of images in different ...
by:Aiforia Technologies  based inCambridge, MASSACHUSETTS (USA)
Automate manual tasks, standardize analysis, and find the hard to spot objects with our cloud-based AI software for image analysis. Aiforia Create is made for seamless use by the medical professional to create and use AI models to increase the speed and accuracy of any image analysis ...
by:Frameshift Labs, Inc.  based inBoston, MASSACHUSETTS (USA)
The engine behind Mosaic. A population-scale variant warehouse enabling complex annotation, phenotype, and genotype queries in ...
by:Frameshift Labs, Inc.  based inBoston, MASSACHUSETTS (USA)
Mosaic is a collaborative platform for organizing, visualizing, and understanding genomic ...
by:SOPHiA Genetics  based inBoston, MASSACHUSETTS (USA)
Metabolic disorders are a major cause of morbidity and mortality, representing a growing health concern worldwide. Over the last decade, substantial progress has been made in the discovery of genetic variants influencing a range of metabolic diseases.1 The advances in next generation sequencing (NGS) technologies have contributed to elucidation of the pathogenic role of variants associated with ...
by:SOPHiA Genetics  based inBoston, MASSACHUSETTS (USA)
Next-generation sequencing (NGS) of the human exome has the potential to identify pathogenic variants responsible for complex phenotypes associated with rare ...
by:SOPHiA Genetics  based inBoston, MASSACHUSETTS (USA)
Alamut Visual Plus™ enables deep assessment of variants on a genomic scale, empowering clinical researchers to make accurate decisions for their data interpretation. Alamut Visual Plus™ is a full genome browser designed to help researchers investigate variations of the human genome. The software combines a wide set of external data with high-quality missense and splicing predictors in ...
by:SOPHiA Genetics  based inBoston, MASSACHUSETTS (USA)
Next-generation sequencing (NGS) has the potential to revolutionize the diagnosis and treatment of cancers and rare diseases but creates extremely large, complex, and noisy datasets for analysis. Without the right analytical technology, pinpointing causative variants and obtaining actionable insights from NGS data requires specialist skills, multiple resources, and considerable time. The ...
by:SOPHiA Genetics  based inBoston, MASSACHUSETTS (USA)
Pioneering Innovation, Streamlining Adoption: We are pushing the boundaries of today’s liquid biopsy capabilities. Bring liquid biopsy to your lab with our streamlined DNA-only NGS workflow, taking you from cell-free DNA sample to comprehensive report in record time. Powered by state-of-the-art proprietary algorithms, the SOPHiA DDMTM Platform reveals deep genomic insights from cell-free ...
by:SOPHiA Genetics  based inBoston, MASSACHUSETTS (USA)
Identifying patterns of genomic scarring in ovarian cancer samples. Accurate identification and reporting of Homologous Recombination Deficiency (HRD) status are critical for better patient management. SOPHiA DDM Dx HRD Solution is a CE-marked in vitro diagnostic (IVD) application leveraging low-pass Whole Genome Sequencing (WGS) and a proprietary deep-learning algorithm. Powered by the advanced ...
by:SOPHiA Genetics  based inBoston, MASSACHUSETTS (USA)
Confidently assess genetic variants predisposing to cancer. Hereditary causes account for ∼10% of cancer cases, and an estimated 20% of cancer patients have a family history of cancer.1 Identification of an individual with a suspected hereditable cancer can lead to additional examinations and help formulate the most appropriate prevention strategies. Evaluating the predisposition to develop ...
by:SOPHiA Genetics  based inBoston, MASSACHUSETTS (USA)
Maximize your biologically actionable insights from small tumor samples with the SOPHiA DDM™ RNAtarget Technology end-to-end solutions. Gene fusions have been associated with various tumors and are recognized as valuable cancer biomarkers in cancer research1. Targeted RNA sequencing is recommended to maximize novel fusion detection by identifying transcribed and potentially actionable ...
by:SOPHiA Genetics  based inBoston, MASSACHUSETTS (USA)
Deeper genomic insights, fewer missed opportunities. CGP enables clinical researchers to identify actionable variants and biomarkers across hundreds of genes using a single solution. The SOPHiA DDMTM Platform offers decentralized, in-house next generation sequencing (NGS) applications that help maximize insights from CGP data by leveraging advanced analytical capabilities, intutive interpretation ...
by:SOPHiA Genetics  based inBoston, MASSACHUSETTS (USA)
Genomic profiling is driving precision oncology. From targeted to comprehensive solutions, Next-Generation-Sequencing (NGS) offers the capacity to simultaneously analyze a select set of genes, regions, and biomarkers based on known involvement across solid tumor such as lung, colon, breast, melanoma, gastric, and ovarian cancers. However, as tests either expand or become more specialized, ...
by:SOPHiA Genetics  based inBoston, MASSACHUSETTS (USA)
Most rare and inherited diseases have a neurological component, likely because more than 80% of human genes are expressed in the brain.1 Neurological disorders are multifactorial and heterogeneous, meaning that their genetic basis is often poorly understood. Indeed, only 30-50% of neurological disorders have a molecular genetic diagnosis.2 ...
by:SOPHiA Genetics  based inBoston, MASSACHUSETTS (USA)
Hematological tumors represent the fourth most frequent cancer type in the developed world. In addition to the continuously evolving clinical guidelines2, harnessing of all the available information when investigating hematological disorders into meaningful insights can be outdated, inaccurate, costly, and time-consuming. This ultimately risks limiting researchers’ productivity, thus ...
by:SOPHiA Genetics  based inBoston, MASSACHUSETTS (USA)
Hereditary causes account for ∼10% of cancer cases, and an estimated 20% of cancer patients have a family history of cancer. Identification of an individual with a suspected hereditable cancer can lead to additional examinations and help formulate the most appropriate prevention strategies. Evaluating the predisposition to develop inherited cancer depends on the ability to characterize genes ...