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Genomics Partnering With Genome Software In Europe
39 software items found
Manufactured by:Alithea Genomics based inEpalinges, SWITZERLAND
Demultiplexing, alignment and gene counts at the click of a ...
by:Qlucore AB based inLund, SWEDEN
Visualization is central in making it easy to understand data. By combining instant visualization with powerful statistics and flexible selection methods, you will be able to see your results ...
by:Qlucore AB based inLund, SWEDEN
Instant exploration is one of the key features in Qlucore Omics Explorer. As a user, you decide your own workflow and starting point. You are in control and can tailor the exploration to meet your specific ...
by:Qlucore AB based inLund, SWEDEN
Qlucore supports a wide variety of data and file formats, see list below. Great flexibility is provided with the Import ...
by:Portable Medical Technology Ltd. based inKillarney, IRELAND
ONCOassist is the go-to app for oncology and haematology professionals. It offers easy access to relevant, up-to-date tools and content when and where it is needed. With the advent of genomic sequencing, combined with an aging population, and new therapies. The decision-making process for oncology/haematology HCP’s is becoming increasingly complex. Unfortunately, there is not always easy ...
by:TriNetX, LLC based inCambridge, MASSACHUSETTS (USA)
The full set of base analytics are enabled on every network, except for anonymous networks such as Linked, where HCO attribution is not shown. With Explore Cohort, review the prevalence of diagnoses, treatments, and procedures among your cohort, retrieve lab value means and standard deviations, and count instances of variants by genome. Use Criteria Analysis to rank order your query ...
by:Lifebit based inHackney, UNITED KINGDOM
It’s challenging to make biomedical data both secure and usable. Lifebit CloudOS brings researcher’s analysis and computation to where the data resides, while enabling them to link other data sources virtually. This translates to faster insights from your data, accelerating patient ...
Manufactured by:Agilent Technologies, Inc. based inSanta Clara, CALIFORNIA (USA)
Agilent's GeneSpring provides powerful, accessible statistical tools for intuitive data analysis and visualization. Designed specifically for the needs of biologists, GeneSpring offers an interactive environment that promotes investigation and enables understanding of Transcriptomics, Metabolomics, Proteomics and NGS data within a biological context. GeneSpring allows you to quickly and reliably ...
by:BC Platforms based inZürich, 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 ...
by:BC Platforms based inZürich, SWITZERLAND
BC|GENOMEis a data management and analysis platform for clinical genomic data production for healthcare organisations and genomics labs. Data is collected and stored on the platform, and users have access to data and tools through an application account. All common data types for NGS, Genotype, and variant analysis can be managed on the platform. BC|GENOME scales up from starting a clinical ...
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:Quretec Ltd based inTartu, ESTONIA
Quretec has made Estonian 2011 census data collection solution, holding world record with 66% of country population participated in the e-census. Qure Data Management Platform is a web-based database software, that can be used for collection, handling, and analysis of data under high quality, security, and robustness requirements. Qure Data Management platform is well suitable for diagnosis or ...
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) 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)
Cardiac diseases are the #1 cause of death globally1,2. Genetic testing is frequently considered a key component of the clinical management process of inherited cardiac disorders, such as hypertrophic, dilated, and arrhythmogenic cardiomyopathies, aortopathies, and inherited arrhythmia syndromes3. This approach is typically reserved for patients with a confirmed or suspected diagnosis of an ...
by:Qlucore AB based inLund, 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. ...
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)
Clinical interpretation has been one of the most complex and time-consuming aspects of transforming genomic data into meaningful results, until ...
Manufactured by:sci2sci UG based inBerlin, GERMANY
VectorCat is an AI-driven platform crafted to streamline the adoption of FAIR principles—Findability, Accessibility, Interoperability, and Reusability—for data management within the biotech and pharmaceutical sectors. It addresses the critical need for proper data governance by ensuring that valuable research insights, experimental outcomes, and regulatory information are not isolated ...
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 ...