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Genomics Software Available In In Canada
76 software items found
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. ...
by:Ovation based inPortland, MAINE (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 ...
by:inDNA Research Labs 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 ...
by:BioDiscovery, A Bionano Genomics Company based inEl Segundo, CALIFORNIA (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 ...
by:PierianDx based inCreve Coeur, MISSOURI (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 software for the analysis, reporting, ...
by:NRGene based inSan Diego, CALIFORNIA (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 real hybrid assembly ...
by:SOPHiA Genetics based inBoston, MASSACHUSETTS (USA)
Deeper genomic insights, fewer missed opportunities. CGP enables clinical researchers to identify actionable variants and biomarkers across hundreds of genes using a single solution. The SOPHiA DDMTM Platform offers decentralized, in-house next generation sequencing (NGS) applications that help maximize insights from CGP data by leveraging advanced analytical capabilities, ...
by:Ovation based inPortland, MAINE (USA)
Ovation's real-world pathogen testing and sequencing data provides the answers researchers need to understand a pathogen's potential impact on human ...
by:PierianDx based inCreve Coeur, MISSOURI (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. ...
by:NRGene based inSan Diego, CALIFORNIA (USA)
Get a jump start on your breeding program even before the greenhouses are up! Identify your desired traits and create your breeding plan in silico with our ready-to-use genomics ...
by:Ovation based inPortland, MAINE (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. ...
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)
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 ...
by:Echelon Diagnostics based inReno, NEVADA (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 ...
by:Karyosoft Inc. based inCarmel, INDIANA (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 life scientists with "anywhere and anytime" ...
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:SoftGenetics, LLC. based inState College, PENNSYLVANIA (USA)
NextGENeLR Software is an effective and easy-to-use resource for the analysis of long read sequencing data such as data from Pacific Biosciences RS, RSII, Sequel, and Sequel II systems, as well as Oxford Nanopore MinION. NextGENeLR can be used for structural variation detection, STR expansion analysis, and whole genome mitochondrial DNA analysis, including low frequency SNV and ...
by:SoftGenetics, LLC. based inState College, PENNSYLVANIA (USA)
It does not require scripting or other bioinformatics support, which are often required when using programs such as CLC Genomics Workbench, Lasergene's SeqMan Pro, as well as academic software such as MAQ & SOAP, Top Hat, BWA & ...
by:NRGene based inSan Diego, CALIFORNIA (USA)
All-to-all linear mapping of multiple denovo assemblies enables intra-species gene content variation exploration. A high-quality reference genome is a great starting point, yet in many plant species the genomic diversity within the species can be as high as 50% of the genomic sequence. The discovery of genomic variations ...
by:Karyosoft Inc. based inCarmel, INDIANA (USA)
Easy to use with just a few clicks and web-based. Flexibility to use single or multiple samples. 41 to 168 days saving for 96 samples. A simple report for whole-genome variant distribution. All your genomic variants information at your ...