Medical Genomics Software For Medical Diagnostics
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based in USA
VIPER automates the screening process from remote patient identification (at the point of diagnosis) to qualified enrollment. Utilizing artificial intelligence, VIPER identifies and matches patients to precision trials in the narrow window of opportunity through lab-agnostic genomic data ingestion, EMR and pathology data in a way that is customized to both the patient and to the research. ...
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based in USA
Easy to use with just a few clicks and web-based. Flexibility to use single or multiple samples. 41 to 168 days saving for 96 samples. A simple report for whole-genome variant distribution. All your genomic variants information at your ...
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based in USA
With our LIMS configurable technology and workflow templates, projects are completed in a fraction of the time and cost of standard LIMS ...
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based in USA
Family Finder provides powerful interactive tools to help find your DNA matches, trace your lineage through time, and determine family connections. ...
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based in USA
Improving The Human Condition Through Data Innovations In Genomics; As an integrated platform, Triton™ brings together clinical data sources in a fully-scalable and customized data warehouse. Leveraging this powerful technology stack, our clients realize actionable and comprehensive results to improve ...
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based in USA
Variant Interpretation * Variant Tracking * Coverage Confirmation Save Time & Resources * Compatible with data from all NGS systems * Targeted Panels and Whole Exome Sequencing. Developed in collaboration with the Laboratory Medicine, Information Technology, and Health Science Research departments of Mayo Clinic, Geneticist Assistant NGS Interpretative Workbench is a unique tool for the ...
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based in USA
Next-generation sequencing (NGS) of the human exome has the potential to identify pathogenic variants responsible for complex phenotypes associated with rare ...
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based in USA
GeneFAX™ is a turn-key conversational AI solution for clinical and genetic testing labs. GeneFAX™ helps labs better engage with their physician-patients- ecosystems through intelligent, remote, and effective interactions which enhances the experience and extends the reach of the organization’s various ...
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based in 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 ...
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by BC Platformsbased in SWITZERLAND
BC|RQUEST as a private service enables availability queries and aggregated analysis on biobanks or internal data silos through a simple web interface for query building and analysis creation. Additionally, BC|RQUEST gives biobanks tools to manage their research project portfolio and research user capability to request and follow projects through integrated ...
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based in USA
CrisprRx provides big data technology applied to gene editing techniques for the advancement of human medicine ...
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based in USA
NLP-based AI for automated mining of clinical documents and reports.Manually extracting clinical data from unstructured text is inefficient. And yet, clinical staff often dedicate up to 30% of their working day repeating just this kind of exercise, and report low levels of satisfaction accordingly. ...
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based in NETHERLANDS
The Observer XT is the ideal tool for many researchers because it saves you time scoring behaviors and it allows you to synchronize and analyze multiple signals (video, audio, physiology, etc) all ...
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based in USA
With our LIMS configurable technology and workflow templates, projects are completed in a fraction of the time and cost of standard Lab Management Software ...
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based in USA
Arming researchers with advanced genomic data analysis and visualization tools. Easy-to-use software provides cutting-edge statistical tools to advance scientific ...
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based in USA
Across the world, numerous initiatives are currently underway to collect massive repositories of genomic and phenotypic data. These data have the potential to reveal transformative insights into the underpinnings of disease, novel therapeutic approaches, and in silico disease models. Seven Bridges ARIATM offers researchers a centralized solution for high throughput molecular and health data ...
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by Qlucore ABbased in SWEDEN
The combination of powerful statistics and instant visualization drives exciting results. Flexibility and expansion are cornerstones. Analyze data using an easy to use statistical model. Integrate and extend the analysis with Python based Templates for scripting. Add statistical methods through the Open API to R. Filter on genomic entities such as read coverage and variants with the NGS module. ...
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based in USA
Bionano's NxClinicalTM Software is the leading copy number variation (CNV) analysis software solution for cytogenetics and molecular laboratories. The latest software (v6.2) release adds three measures of genomic instability for homologous recombination repair deficiency (HRD) in solid tumors: Loss of heterozygosity (LOH). Telomeric Allelic Imbalance (TAI). Large-Scale State Transitions (LST). ...
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by NRGenebased in USA
All-to-all linear mapping of multiple denovo assemblies enables intra-species gene content variation exploration. A high-quality reference genome is a great starting point, yet in many plant species the genomic diversity within the species can be as high as 50% of the genomic sequence. The discovery of genomic variations is a hot scientific subject in many research papers, but current ...
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Manufactured by Fusion Genomics Corporationbased in CANADA
FUSIONCloud is the final component in FUSION GENOMICS’ ONETest platform. It is a secure and compliant bioinformatics platform for sensitive and multiplexed pathogen identification from (NGS) data generated by the ONETest molecular diagnostic assay ...
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