Genomics Software
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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 ISRAEL
Phenome One’s revolutionary Genomics module (a.k.a. Unity) uses advanced GWAS and QTL analysis and standardized terminology to identify the genetic markers affecting the traits you are looking for. The Genomics module allows you to see the big picture, by evaluating marker effects on phenotypes not only in your study but also in ...
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based in INDIA
OncoNGx Genomic Workbench is a HIPAA compliant cloud based informatics and clinical annotation platform that will translate sequence (NGS) data from a Cancer diagnostic gene panel into actionable report/information for ...
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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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by Ovationbased in USA
Ovation's genomic data solutions enable life science and biopharma companies to accelerate research and development across a wide range of therapeutic areas including autoimmune, metabolic, and infectious ...
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based in USA
Mosaic is a collaborative platform for organizing, visualizing, and understanding genomic ...
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based in USA
Genomic testing is a management tool that is available to producers to determine the genetic merit of a dairy animal. Modeled after the traditional phenotypic indexes (which are based on actual production, reproductive data, and type information), genomic testing reads the DNA of an animal and produces predicted transmitting ability ...
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based in FRANCE
The integrated genomic analysis solution that delivers accurate results with increased efficiency and fast turnaround ...
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based in USA
As described in Chaubey et al., Journal of Molecular Diagnostics, vol. 22, No. 6 June 2020, they used 10x WGS and validated that the NxClinical algorithm detected all CNVs and AOH that were found by high-resolution SNP arrays. Figure 2. shows a small exonic deletion detected using 10x WGS with the MSR algorithm. With higher depth NGS, smaller CNVs can be detected and integrated with sequence ...
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by PierianDxbased in USA
Clinical Genomics Workspace helps you provide accurate, timely, and actionable results for patients. Developed initially by one of the first medical institutions to launch next generation sequencing tests for cancer and complex inherited diseases, Clinical Genomics Workspace provides a streamlined and clinically integrated ...
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by NRGenebased in USA
Receive the highest genome assembly quality in a record time. DeNovoMAGIC™ has already been successfully used by hundreds of customers around the globe, building the most challenging reference genomes. Now, with the availability of an accurate long read data our quality got even better. The newest version of DenovoMAGIC™ employs a ...
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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 ...
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by PierianDxbased in USA
Where Human Experts Meet Best-In-Class Technology. We offer the world’s most clinically robust, intelligent knowledgebase fueled by expert content curation, an extensive rules engine, and machine learning. ...
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by Ovationbased in USA
Ovation's real-world pathogen testing and sequencing data provides the answers researchers need to understand a pathogen's potential impact on human ...
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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 ...
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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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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 ...
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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 ...
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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
Accelerates "Time to Market" for your innovations by saving time for life scientists and bioinformaticians. Increases value to your organizations by serving as a repository for all your genomics data including historical data saving data preparation time and drives new innovations. Saves cost through increased efficiency by empowering ...
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