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Genome Comparative Genome Software Near Kenya
136 software items found
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Manufactured by:Analytik Jena - an EndressHauser Company based inJena, GERMANY
Destination Lab Automation stands as a milestone for liquid handling and lab automation because we add substance to all the talk about the potential of lab automation for the pharmaceutical and life science industries. With strong customer focus and deep market experience, Analytik Jena with its CyBio product line is a leading brand for high quality liquid handling and automation technologies. ...
by:Partek Incorporated based inChesterfield, MISSOURI (USA)
Partek® Pathway™ allows you to explore complex biological relationships and pathways between genes to discover meaningful biological insights. You can calculate pathway enrichment, detect disrupted or influential pathways, search for specific pathways and genes, and color code genes based on their p-values and fold changes. Partek Pathway integrates inside Partek Flow or Partek Genomics ...
Manufactured by:Alithea Genomics based inEpalinges, SWITZERLAND
Demultiplexing, alignment and gene counts at the click of a ...
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 sequencing. The ...
by:Qlucore AB based inLund, SWEDEN
Visualization is central in making it easy to understand data. By combining instant visualization with powerful statistics and flexible selection methods, you will be able to see your results ...
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 to benefit the data quality and ...
by:BC Platforms based inZürich, SWITZERLAND
BC|INTERPRET Cloud is BC Platforms’ interpretation service (running on your chosen cloud provider). This service links several BC Platforms reporting partners (Wellness, PGx, Ancestry etc.) via 2-way integration between the reporting partner and your system, allowing you to offer end customers various kinds of interpretation reports, especially from genotyping ...
by:FamilyTreeDNA based inHouston, TEXAS (USA)
Family Finder provides powerful interactive tools to help find your DNA matches, trace your lineage through time, and determine family connections. ...
by:Qlucore AB based inLund, SWEDEN
Instant exploration is one of the key features in Qlucore Omics Explorer. As a user, you decide your own workflow and starting point. You are in control and can tailor the exploration to meet your specific ...
by:Echelon Diagnostics based inReno, NEVADA (USA)
CrisprRx provides big data technology applied to gene editing techniques for the advancement of human medicine ...
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:Bionano based inSan Diego, CALIFORNIA (USA)
Bionano Access provides all the software needed for experiment management, visualization and analysis of Bionano genome mapping data in one place. This web-based hub for Saphyr operations allows the user to set up runs and monitor real-time data quality metrics remotely, as well as visualize and manipulate maps and structural variants. Video tutorials are available here that will guide you ...
by:Karyosoft Inc. based inCarmel, INDIANA (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 ...
by:Qlucore AB based inLund, SWEDEN
Qlucore supports a wide variety of data and file formats, see list below. Great flexibility is provided with the Import ...
by:NRGene based inSan Diego, CALIFORNIA (USA)
The cannabis haploid genome is comprised of 735 million base pairs (Mbp). It is highly heterozygous, which means most of the regions (loci) along the genome carry two dissimilar sequences (alleles). Most assembly tools generate a synthetic (haploid) genome, resulting in a sequence for cannabis that is typically a mix (chimera) of both alleles. NRGene’s DeNovoMAGIC assembly tool takes ...
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 population ...
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. It is platform independent and much simpler to ...
by:Igenbio, Inc. based inChicago, ILLINOIS (USA)
Quickly analysis your raw sequence files with ERGO’s integrated variant detection and annotation workflows. ERGO’s automatic workflows provide fast and accurate variant calling using academically proven software yielding rigorous results you can rely ...
by:BioDiscovery, A Bionano Genomics Company based inEl Segundo, CALIFORNIA (USA)
BioDiscovery has developed two algorithms for the detection of CNV and AOH events from NGS using its decades-long expertise in the area. One algorithm, the “Self-reference” algorithm, can be used for all WGS data regardless of sequencing depth. The second is the “Multi-Scale Reference” (MSR) algorithm that is applicable to all NGS data (WGS, WES, and Gene panels). The MSR ...
by:Advaita Bioinformatics based inAnn Arbor, MICHIGAN (USA)
iVariantguide allows you to quickly analyze and interpret your VCF file with publication-ready visualizations. Single sample, Tumor/Normal, Pedigree, and Group v. ...