- Home
- Software
- usa california
- genomes
Refine by
Genomes Software In Usa California
26 software items found
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: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: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: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: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: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 ...
Manufactured by:Mammoth Biosciences, Inc. based inBrisbane, CALIFORNIA (USA)
Enhanced genome editing with an expanded CRISPR toolkit: Our CRISPR-Cas systems provide unprecedented power to edit the ...
by:BioDiscovery, A Bionano Genomics Company based inEl Segundo, CALIFORNIA (USA)
The MSR algorithm is able to create “virtual” bins with sizes proportional to the expected number of reads offering high-resolution detection of events in areas of interest (e.g. exons) while also providing a nice genome-wide ...
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: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: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: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 criteria in the ...
by:BioDiscovery, A Bionano Genomics Company based inEl Segundo, CALIFORNIA (USA)
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 with genomic scarring, such as Loss of Heterozygosity (LOH), telomeric allelic imbalances (TAI), and large-scale state transitions (LST) can be visualized and manually called with confidence. ...
by:Seven Bridges Genomics based inCharlestown, MASSACHUSETTS (USA)
It is a central hub for teams to store, analyze, and jointly interpret their bioinformatic data. The Platform co-locates analysis pipelines alongside the largest genomic datasets to optimize processing. It allocates storage and compute resources on demand, to meet the needs of ever-growing ...
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. ...
Manufactured by:Ultima Genomics based inFremont, CALIFORNIA (USA)
Our integrated analysis tools are optimized for speed, cost-efficiency, flexibility and accuracy for high quality omics data at ...
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:BioDiscovery, A Bionano Genomics Company based inEl Segundo, CALIFORNIA (USA)
The most recent version of NxClinical, the leading copy number variation (CNV) analysis software for clinical cytogenetics and molecular labs, now includes an integrated ACMG guidelines scoreboard ...
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 ...