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Genomics Analysis Software Near Malawi
23 software items found
by:SeqOne S.A.S. based inMontpellier, FRANCE
The integrated genomic analysis solution that delivers accurate results with increased efficiency and fast turnaround ...
by:NRGene based inSan Diego, CALIFORNIA (USA)
Pave the way to smarter breeding by unraveling the causation elements in your population genomics. Quickly discover the phenotype-genotype correlations in any organism with NRGene’s complete trait-mapping package. We’ll generate a high-resolution recombination map which is used to reveal the complete segregation pattern in each progeny. Our special ...
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:TriNetX, LLC based inCambridge, MASSACHUSETTS (USA)
With Explore Cohort, review the prevalence of diagnoses, treatments, and procedures among your cohort, retrieve lab value means and standard deviations, and count instances of variants by genome. Use Criteria Analysis to rank order your query criteria by the number of patients they disqualify. Rate of Arrival predicts the volume of new patients who will meet your ...
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" access, analyze ...
by:Partek Incorporated based inChesterfield, MISSOURI (USA)
Partek® Genomics Suite® is a statistical analysis software that lets you analyze microarray, qPCR, and pre-processed NGS data right from your desktop computer. It is fast, agile, and memory efficient. With a user-friendly interface, rich visualizations, and guided workflows for common genomics assays, Partek Genomics ...
Manufactured by:Agilent Technologies, Inc. based inSanta Clara, CALIFORNIA (USA)
Agilent's GeneSpring provides powerful, accessible statistical tools for intuitive data analysis and visualization. Designed specifically for the needs of biologists, GeneSpring offers an interactive environment that promotes investigation and enables understanding of Transcriptomics, Metabolomics, Proteomics and NGS data within a biological context. GeneSpring allows you to quickly and reliably ...
by:BioDiscovery, A Bionano Genomics Company based inEl Segundo, CALIFORNIA (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). ...
Manufactured by:10x Genomics based inPleasanton, PENNSYLVANIA (USA)
10x Genomics Cloud Analysis is a platform for data management, analysis, and collaboration to streamline and accelerate the interpretation of data generated from 10x Genomics assays. Currently only available in the United ...
by:BC Platforms based inZürich, SWITZERLAND
BC|RQUEST as a private service enables availability queries and aggregated analysis on biobanks or internal data silos through a simple web interface for query building and analysis creation. Additionally, BC|RQUEST gives biobanks tools to manage their research project portfolio and research user capability to request and follow projects through integrated ...
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 ...
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:Qlucore AB based inLund, SWEDEN
Flexibility and expansion are cornerstones. Analyze data using an easy to use statistical model. Integrate and extend the analysis with Python based Templates for scripting. Add statistical methods through the Open API to R. Filter on genomic entities such as read coverage and variants with the NGS module. Use the GSEA workbench, the kmeans++ clustering or ...
by:BioDiscovery, A Bionano Genomics Company based inEl Segundo, CALIFORNIA (USA)
Arming researchers with advanced genomic data analysis and visualization tools. Easy-to-use software provides cutting-edge statistical tools to advance scientific ...
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. ...
by:Seven Bridges Genomics based inCharlestown, MASSACHUSETTS (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 solution for high throughput molecular and ...
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)
GeneMarker®HTS software provides a validated streamlined workflow for forensic mitochondrial , STR, and Y-STR casework as well as medical research of mitochondrial DNA from massively parallel squencing platforms (MPS) - such as the Illumina® and Ion Torrent® - in an easy-to-use Windows® operating system. ...
by:NRGene based inSan Diego, CALIFORNIA (USA)
Would you like to stack all the best traits in one new variety, but not sure where to begin? Our genetics experts will support you in starting a breeding program, using your own genetics to discover markers you can use to create varieties with the best characteristics. Let us help you create the plant you've ...
by:Agronomix Software Inc. based inWinnipeg, MANITOBA (CANADA)
Develop hybrids and varieties faster, more efficiently and with greater precision via bioinformatics tools integrated into your breeding ...