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Genomics Software Available In Iran
67 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:Phenome Networks based inRehovot, 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 different experiments and ...
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: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: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: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 ...
Manufactured by:10x Genomics based inPleasanton, PENNSYLVANIA (USA)
Loupe Browser is a powerful visualization software that provides intuitive analysis functionality you need to explore your 10x Genomics data. This easy-to-use desktop application for Windows and MacOS is available at no cost, enabling anyone to uncover biological insights from their ...
Manufactured by:Fusion Genomics Corporation based inBurnaby, BRITISH COLUMBIA (CANADA)
FUSION GENOMICS ONETest platform offers a complete 12 hours “Benchtop to Desktop” solution for next generation sequencing based diagnostic testing of infectious diseases. The ONETest platform comprises our patent pending and proprietary UNIPrep, QUANTUMProbes and the FUSIONCloud with 1000X the sensitivity over PCR and up to 9000X target enrichment over metagenome ...
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 ...
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 ...