- Home
- software
- usa california
- genomics redefines the boundaries of fungal genomics
Refine by
Genomics Redefines The Boundaries Of Fungal Genomics Software In Usa California
22 software items found
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: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: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: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: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 ...
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 is a hot scientific subject in many research papers, but current ...
by:DNAnexus, Inc. based inMountain View, CALIFORNIA (USA)
Partnerships fuel scientific advancements. Whether you are working together across hallways or international borders, DNAnexus Portals™ deliver a secure, fit-to-purpose, branded, online workspace that enables cross-disciplinary collaboration, scales data and pipeline distribution, and allows unique engagement with your ...
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:Optrahealth Inc based inSan Jose, CALIFORNIA (USA)
GeneFAX™ is a turn-key conversational AI solution for clinical and genetic testing labs. GeneFAX™ helps labs better engage with their physician-patients- ecosystems through intelligent, remote, and effective interactions which enhances the experience and extends the reach of the organization’s various ...
by:BioDiscovery, A Bionano Genomics Company based inEl Segundo, CALIFORNIA (USA)
The most comprehensive and up-to-date solution for cytogenetics and molecular genetics in one system for analysis and interpretation of all genomic variants from microarray and NGS ...
by:Strateos Inc. based inMenlo Park, CALIFORNIA (USA)
Use our Platform to overcome the challenges associated with generating biologically relevant, clean and structured data to advance R&D. The Strateos Platform automates chemistry, biology, and tissue analysis into closed loop robotic labs that accelerate drug discovery programs. Through a combination of best-in-class robotics and control systems, advanced software for imaging and analytics, ...
by:PointCross Life Sciences Inc. based inFoster City, CALIFORNIA (USA)
A format agnostic solution for harmonization across clinical, molecular biomarker, nonclinical and preclinical data for searchable cross study ...
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:TriNetX, LLC based inCambridge, MASSACHUSETTS (USA)
Data sourced from the EHRs of U.S. healthcare organizations forms the foundation of this combined data asset, providing a rich clinical picture of patients from encounters with providers, lab results, procedures, medication orders, and genomics. Medical and pharmacy claims provide insight into a patient’s care before and after these encounters, regardless of provider. Pre-existing ...
by:DNAnexus, Inc. based inMountain View, CALIFORNIA (USA)
DNAnexus Titan™ powers the future of genomics research and clinical pipelines with trusted, high-performance data analysis ...
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:AgriTech Analytics based inVisalia, CALIFORNIA (USA)
The fee schedule below with all of its footnotes is available at CDCB Fee Schedule Update 4-03-2019. Included below is the schedule. Additional information on changes regarding crossbred animals can be found at Genomic Evaluations Including Crossbred ...
by:CareDx, Inc based inSouth San Francisco, CALIFORNIA (USA)
Every minute of laboratory time is valuable. AlloSeq HCT can help you save time with a simple workflow and powerful analysis software, all while achieving high sensitivity chimerism monitoring. Engraftment monitoring (chimerism) testing evaluates the success of a hematopoietic stem cell transplant by measuring the relative ratio of the recipient and the donor cell population in the ...