Vertebral Compression Fracture Software
12 software items found
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:Advaita Bioinformatics based inAnn Arbor, MICHIGAN (USA)
iVariantguide allows you to quickly analyze and interpret your VCF file with publication-ready visualizations. Single sample, Tumor/Normal, Pedigree, and Group v. ...
by:Karyosoft Inc. based inCarmel, INDIANA (USA)
A central repository for all your millions of SNPs and Indels. Data organized in project specific and/or organism specific (microbes, animals, plants, humans and more). Hosted on your internal servers or any cloud servers. No more data loss; No need to open on excel. Web-based and user-friendly for anywhere and anytime on any ...
by:ArrayGen Technologies based inPune, INDIA
The ANG genome browser is a visualization tool, developed by ArrayGen Technologies Pvt. Ltd. This is a fast and an efficient genome browser, built with Javafx and Java swing. ANG Genome Browser was built for latest next generation sequencing data analysis. It is platform independent and much simpler to ...
by:SoftGenetics, LLC. based inState College, PENNSYLVANIA (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 ...
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:Molecular Health GmbH based inHeidelberg, GERMANY
Use worldwide knowledge to reliably determine the risk of genetic disease. MH Guide/Mendel is optimized for the evaluation of germline variants associated with hereditary diseases. The software application is a module of MH Guide and supports human geneticists in the evaluation of germline variants. Just like MH Guide, MH Guide/Mendel analyzes gene variants in comparison with data from Dataome, ...
by:BC Platforms based inZürich, SWITZERLAND
BC | INSIGHT is a data and research management solution for clinical genomics studies. Genomic and phenotypic 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, GWAS, variant analysis, linkage, and other statistics can be managed on the platform. BC|INSIGHT scales up from small candidate gene studies ...
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 ...
Manufactured by:OncoDNA S.A. based inGosselies, BELGIUM
OncoKDM® is an online platform that turns your NGS data into actionable clinical information. Moreover, OncoKDM® can integrate NGS results with IHC, MSI and TMB data. The resulting comprehensive and interactive report includes updated information about approved and investigational treatments for each patient, as well as NGS quality control data, patient clinical data and comprehensive NGS ...
by:Igenbio, Inc. based inChicago, ILLINOIS (USA)
ERGO 2.0 provides a systems biology informatics toolkit centered on comparative genomics to capture, query, and visualize sequenced genomes. Using Igenbio's proprietary algorithms, and the most comprehensive genomic database integrated with the largest collection of microbial metabolic and non-metabolic pathways, ERGO™ assigns functions to genes, integrates genes into pathways, and ...
by:SeqOne S.A.S. based inMontpellier, FRANCE
The integrated genomic analysis solution that delivers accurate results with increased efficiency and fast turnaround ...