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Genomics Redefines The Boundaries Of Fungal Genomics Software In North America
76 software items found
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 ...
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 ...
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
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: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 ...
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 ...
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: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:Frameshift Labs, Inc. based inBoston, MASSACHUSETTS (USA)
Mosaic is a collaborative platform for organizing, visualizing, and understanding genomic ...
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. ...
by:CareDx, Inc based inSouth San Francisco, CALIFORNIA (USA)
AlloSeq® Tx 17 is an innovative NGS HLA typing solution that uses Hybrid Capture Technology, which eliminates the inefficiencies and limitations of traditional Long-Range PCR methods. AlloSeq Tx 17 goes beyond the traditional transplant related loci to consider more transplant associated genes and helps you to identify the best genetic ...
by:TriNetX, LLC based inCambridge, MASSACHUSETTS (USA)
The full set of base analytics are enabled on every network, except for anonymous networks such as Linked, where HCO attribution is not shown. 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 ...
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: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 ...
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:CosmosID based inGermantown, MARYLAND (USA)
The CosmosID-HUB is an online software solution that enables incredibly fast and easily accessible analysis of complex metagenomic data. The app gives scientists user-friendly access to numerous pipelines developed by CosmosID, including amplicon and shotgun data analysis. In addition to having access to version-controlled, validated pipelines, the software enables continuous splicing of ...
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:Molsoft LLC based inSan Diego, CALIFORNIA (USA)
ActiveICM (US Patent No:7,880,738) enables you to view and display 3D ICM graphical slides and animations interactively inside Microsoft PowerPoint and web browsers such as Internet Explorer, Safari and Mozilla Firefox. The files can be prepared and saved in ICM Browser, ICM Browser Pro or ICM Pro. ActiveICM is being used for scientific publishing by journals such as PLoS ONE and Nature. Please ...
by:BioDiscovery, A Bionano Genomics Company based inEl Segundo, CALIFORNIA (USA)
The MSR algorithm can be applied to any gene panel from single gene (e.g. DMD test) to large panels having thousands of gene. The image below is from the Illumina TruSightTM Oncology 500 (TSO500) panel showing a somatic cancer profile. The cytogenetic complexity of the tumor sample is clearly evident with a large copy number gain of 8p and loss of a large section of 13q. Aberrations associated ...