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Bioinformatics Software In Europe
12 software items found
Manufactured by:CENTOGENE N.V. based inRostock, GERMANY
Analyze, interpret, and report genomic variants with our decentralized diagnostic solution – no matter where you are located. CentoCloud is a cloud-based Software as a Service (SaaS) platform specifically designed for the rapid bioinformatic analysis and interpretation of Next-Generation-Sequencing (NGS) data based on CENTOGENE’s proprietary Biodatabank and external ...
by:Champions Oncology, Inc. based inHackensack, NEW JERSEY (USA)
Lumin Bioinformatics is a dynamic analytic and visualization software that empowers cancer biologists to harness the power of computational science in a convenient and sophisticated tool. The power of Lumin is in the ability to explore and perform analysis on rich and unique datasets assembled from over 12,000 cancer patients, including thousands of clinical treatment responses ...
by:Seven Bridges Genomics based inCharlestown, MASSACHUSETTS (USA)
The Seven Bridges Platform is a cloud-based environment for conducting bioinformatic analyses. It is a central hub for teams to store, analyze, and jointly interpret their bioinformatic data. The Platform co-locates analysis pipelines alongside the largest genomic datasets to optimize processing. It allocates storage and compute resources on demand, to meet the ...
by:SOPHiA Genetics based inBoston, MASSACHUSETTS (USA)
As a result, Alamut Visual Plus™ decreases the time and effort required to assess the pathogenicity of genomic variants while maximizing lab workflow efficiency. Furthermore, visualization of different bioinformatics formats is now available in parallel, including Sanger, VCF, BED, and BAM files. Researchers can now also benefit from a simultaneous display of multiple genes ...
by:Enpicom B.V. based ins-Hertogenbosch, NETHERLANDS
Pick and choose from our specialized Apps to compose the desired end-to-end workflow to answer your biological ...
by:Champions Oncology, Inc. based inHackensack, NEW JERSEY (USA)
Cell Line Select® is Champions' online, searchable database containing over 100 Human cancer cell lines, including characterization datasets such as gene mutations identified through Whole Exome Sequencing (WES) and gene expression levels quantified using RNASeq technology. ...
by:Qlucore AB based inLund, SWEDEN
Ongoing work to comply with the CE-IVDR (clinical use). The program includes classifier models and supportive gene fusion analysis. Qlucore Diagnostics is a scalable diagnostic solution from data to report, improving clinical? workflow? with easy-to-understand analysis and visualization? for better communication between lab, clinicians, and ...
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)
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:Seven Bridges Genomics based inCharlestown, MASSACHUSETTS (USA)
The representation of the human reference genome as a linear haploid DNA sequence poses limitations when trying to incorporate the known genetic diversity of human populations. This has led to the development of graph-based references, able to naturally represent all polymorphisms, including insertions, deletions, and structural ...
by:SeqOne S.A.S. based inMontpellier, FRANCE
The integrated genomic analysis solution that delivers accurate results with increased efficiency and fast turnaround ...
by:SOPHiA Genetics based inBoston, MASSACHUSETTS (USA)
Enabling novel fusion detection in small samples to improve lung cancer management. Sensitive novel fusion detection optimized for small lung cancer FFPE biopsies enhance patient care. SOPHiA DDM™ Dx RNAtarget Oncology Solution (ROS) is a CE-marked in vitro diagnostic (IVD) application based on next-generation sequencing (NGS) enabling accurate and sensitive detection of novel ...