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Genomics Software Vendor Serving Peru
37 companies found
Software vendorbased inCreve Coeur, MISSOURI (USA)
Pierian guides healthcare organizations to develop NGS testing programs onsite and support their growth through our best-in-class technology and services. We partner with clinicians and medical facilities to advance clinical genomics and modernize ...
Where Human Experts Meet Best-In-Class Technology. We offer the world’s most clinically robust, intelligent knowledgebase fueled by expert content curation, an extensive rules engine, and machine learning. ...
Software vendorbased inPhiladelphia, PENNSYLVANIA (USA)
With extensive experience optimising processes for analytical, production and R&D laboratories across multiple industries and regulatory environments, we provide consistent, quality informatics solutions. We operate on a truly global basis, serving ...
Software vendorbased inMountain View, CALIFORNIA (USA)
DNAnexus has built the world’s most secure cloud platform and global network for scientific collaboration and accelerated discovery. We embrace challenges and partnership to tackle the world’s most exciting opportunities in human health. We are ...
DNAnexus Titan™ powers the future of genomics research and clinical pipelines with trusted, high-performance data analysis ...
Software vendorbased inLund, SWEDEN
Our mission is to make it easier to analyze the huge amounts of complex data that are generated by innovations in the fields of genetics and proteomics. We do this by providing powerful visualization-based bioinformatics data analysis tools for ...
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 ...
Software vendorbased inCambridge, MASSACHUSETTS (USA)
TriNetX is the global health research network that connects the world of drug discovery and development from pharmaceutical company to study site, and investigator to patient by sharing real-world data to make clinical and observational research ...
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 ...
Software vendorbased inPak Shek Kok, HONG KONG
Artificial intelligence for every step of pharmaceutical research and development. Our mission is to accelerate drug discovery and drug development by continuously inventing and deploying new artificial intelligence technologies. We provide AI ...
Software vendorbased inSan Diego, CALIFORNIA (USA)
NRGene is a Genomics company that provides turn-key solutions. Relying on a vast proprietary database and AI-based technologies, we provide the largest seed and food companies in the world with the computational tools they need to maximize their ...
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 ...
Software vendorbased inTartu, ESTONIA
Quretec Ltd. was established in 2006 as a software company building upon unique skills in data management solutions. The team was established in 2002 as an IT department of EGeen, a venture that started with a goal to collect and analyze the DNA ...
Software vendorbased inHackney, UNITED KINGDOM
Lifebit has created a patented technology that enables researchers to run analyses on multiple, distributed datasets in-situ and avoid risky movement of highly-sensitive data. Lifebit empowers therapeutic leaders and pioneers in precision medicine ...
Software vendorbased inCarmel, INDIANA (USA)
Karyosoft, a fast-growing genomics software and data science start-up company, empowers life scientists to effectively manage, democratize, and quickly transform a vast amount of genomics data into innovations within their secured on-premise or ...
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 ...
Software vendorbased in, INDIA
inDNA Research Labs is an early stage big-data analytics healthcare startup that is at the forefront of trying to bring comprehensive genomic analysis to routine clinical care. Our goal is to democratize the use of genomics technologies by ...
OncoNGx Genomic Workbench is a HIPAA compliant cloud based informatics and clinical annotation platform that will translate sequence (NGS) data from a Cancer diagnostic gene panel into actionable report/information for ...
Software vendorbased inBoston, MASSACHUSETTS (USA)
At PathAI, we’re dedicated to improving patient outcomes with reliable AI-Powered technology and meaningful collaboration with biopharma, laboratories, and clinicians — aiming to provide patients with access to accurate diagnoses and effective ...
Software vendorbased inBoston, MASSACHUSETTS (USA)
SOPHiA GENETICS is the creator of a global data-sharing network – we work with customers from over 790 institutions in over 70 countries. Our network advances data-driven medicine to improve health outcomes and economics worldwide. We offer a ...
Clinical interpretation has been one of the most complex and time-consuming aspects of transforming genomic data into meaningful results, until ...
Software vendorbased inSecaucus, NEW JERSEY (USA)
Quest Diagnostics empowers people to take action to improve health outcomes. Derived from the world's largest database of clinical lab results, our diagnostic insights reveal new avenues to identify and treat disease, inspire healthy behaviors and ...
Software vendorbased inEl Segundo, CALIFORNIA (USA)
BioDiscovery has been an established leader in genomic bioinformatics for more than 23 years with a mission of improving patient care through effective use of genomic data. Our platform agnostic approach allows customers to use data from any ...
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 ...
Software vendorbased inPortland, MAINE (USA)
Ovation advances human health by enabling the use of molecular and human genomic data at scale for researchers developing precision medicines. We’re on a mission to advance human health by enabling the use of molecular and human genomic data at ...
This Ovation IBD Genomic and Clinical Linked Data sample dataset is a packaged, real-world observational cohort of 10 Inflammatory Bowel Disease (IBD) subjects. It's available at no cost for scientists interested in evaluating ...
Software vendorbased inCambridge, MASSACHUSETTS (USA)
The exponential growth of biomedical data, driven by the adoption of electronic medical records (EMRs), provides an unprecedented opportunity to create transformative technologies and products in healthcare. nference partners with medical centers to ...
Software vendorbased inNew York City, NEW YORK (USA)
Led by a team of experts in the fields of life sciences, oncology, pathology, technology, machine learning, and healthcare, Paige strives to transform cancer diagnostics. We make it possible not only to provide additional information from digital ...
Software vendorbased inChicago, ILLINOIS (USA)
Igenbio, Inc. develops genome analysis products and services for the life science industry. Our scientists have broad experience in both in silico and wet lab sequencing, research and development with more than 100 relevant publications in these ...
ERGO 2.0 provides a systems biology informatics toolkit centered on comparative genomics to capture, query, and visualize sequenced genomes. Using Igenbio's proprietary algorithms, and the most comprehensive ...
Software vendorbased inTampa, FLORIDA (USA)
Inspirata, Inc. helps patients fighting cancer, and the clinicians they trust, make every moment matter. Our comprehensive cancer informatics solutions bring together disparate data throughout the entire cancer care journey to drive informed ...
