Vertebral Compression Fracture Software Available In Latin America
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by Qlucore ABbased in SWEDEN
Qlucore supports a wide variety of data and file formats, see list below. Great flexibility is provided with the Import ...
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based in 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 ...
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based in 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 ...
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based in USA
iVariantguide allows you to quickly analyze and interpret your VCF file with publication-ready visualizations. Single sample, Tumor/Normal, Pedigree, and Group v. ...
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Manufactured by Bionanobased in USA
Bionano Data Solutions includes a complete suite of hardware and software for end-to-end experiment management, analysis and bioinformatics processing, along with convenient web-based management and monitoring ...
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based in 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 ...
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based in 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 ...
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based in 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, ...
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by BC Platformsbased in 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 ...
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Manufactured by OncoDNA S.A.based in 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 ...
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based in 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 ...
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by Ovationbased in USA
This Ovation IBD Genomic and Clinical Linked Data sample dataset is a packaged, real-world observational cohort of 10 Inflammatory Bowel Disease (IBD) subjects. It's available at no cost for scientists interested in evaluating Ovation’s Whole Genome Sequencing and RNAseq data with up to 30x coverage. The data is linked with clinical data, including full redacted pathology reports, ...
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