Alternatives to Kanteron

Clara's domain specific tools, AI pretrained models, accelerated applications, and accelerated AI applications are enabling AI advances in many fields, including medical device, imaging, drug discovery and genomics. Holoscan allows you to explore the entire pipeline of medical device deployment and development. With the NVIDIA IGX Developer Kits, you can build containerized AI apps using the Holoscan SDK. The NVIDIA IGX SDK includes pre-trained AI model, healthcare-specific acceleration libraries and reference applications for medical devices.

All-in-One LIMS, ELN, QMS, and DMS Platform Xybion LIMS is an all-inclusive Digital Laboratory system including LIMS, ELN, QMS, and DMS that creates optimized workflows for the unique business needs of all regulated laboratories including research, diagnostics, quality control, stability studies, and more. Xybion LIMS instills consistency, improves data quality, and supports regulatory compliance with a complete laboratory management solution that connects with your operating systems with powerful laboratory information management and analytics.

Ibex Medical Analytics is a pioneer in AI-powered pathology cancer diagnosis. We are a multidisciplinary group of entrepreneurs, data scientists and software engineers, who work together to realize our vision of transforming cancer diagnosis with AI and improving patient care. As the number of cancer tests increases each year, pathologists face increasing challenges in providing accurate and timely analysis. Ibex uses artificial Intelligence (AI) to create clinical-grade solutions that detect cancer as accurately and quickly as a human pathologist. Galen Platform uses algorithms that analyze images and grade cancer in biopsies. It also points to other clinically important findings. This helps pathologists reduce diagnostic errors and improve efficiency. Galen™, Breast and Galen™, Prostate are the first AI-based cancer detection solutions that Ibex has ever used in routine clinical practice in pathology laboratories. They have been proven to be able to detect missed cases.

To drive precision medicine programs that work, pharmaceutical companies require comprehensive genomic information. However, decisions are often made with only 10% of the data available. Genomenon provides 100% of the data. ProdigyTM Patient Landscapes are a cost-effective and efficient natural history research solution for pharmaceuticals. They enhance insights from retrospective and prospective health data to support the development rare disease therapies. Genomenon uses an AI-driven approach to deliver a thorough and expert assessment of all patients in the medical literature in a fraction time. Get a complete overview of every genomic biomarker in the medical literature. Every scientific assertion is supported with empirical evidence from medical literature. Identify all genetic drivers and determine which variants are pathogenic according ACMG clinical standards.

Eidogen-Sertanty’s Target Informatics platform (TIP), is the first global structural informatics system. It enables researchers to examine the druggable genome from an structural perspective. TIP increases the rapidly expanding body experimental protein structure information and transforms structure based drug discovery from an inefficient, data-scarce discipline to a high-throughput science with rich data. TIP is a tool that bridges the knowledge gap between bioinformatics (bioinformatics) and cheminformatics. It provides drug discovery researchers with a knowledge bank of information that is both unique and highly complementary to existing bio- and cheminformatics platform information. TIP's seamless integration between structural data management technology and unique target-to-lead analysis capabilities enhances every stage of the discovery pipeline.

We are a biotechnology company in clinical stage. We decode biology by integrating technological innovations across biology and chemistry to industrialize drug discovery. CRISPR genome editing and synthetic Biology allow for greater control over biology. Advanced robotics allows for reliable automation of complex laboratory research on an unprecedented scale. Neural network architectures allow for iterative analysis and inference from large, complex, in-house data sets. Cloud solutions increase the flexibility of high-performance computation. To build a next-generation biopharmaceutical business, we are using new technology to create virtuous learning cycles around datasets. A synchronized combination hardware, software, and data that is used to industrialize drug discovery. Redefining the traditional drug discovery process. One of the most extensive, broadest, and deepest pipelines in any technology-enabled drug company.

Geneious Prime makes bioinformatics more accessible by transforming raw information into visualizations which make sequence analysis intuitive. Simple assembly of sequences and easy editing contigs. Automatic annotation of gene prediction, motifs and translation. Genotype microsatellite trace with automated ladder fitting, peak calling, and generation of tables of alleles. A highly customizable sequence view displays beautiful visualizations of annotated assemblies and genomes. SNP variants analysis with powerful SNPs, RNA-Seq analysis and amplicon metagenomics. Create your own searchable database of primers for PCR and sequencing and design and test them. Geneious Biologics offers a flexible, scalable and secure way to streamline antibody analysis workflows. It allows you to create high-quality libraries, and select the best therapeutic candidates.

DNAnexus Apollo™, accelerates precision drug discovery through collaboration that draws critical insights from omics data. Precision drug discovery requires the collection and analysis of large volumes of clinical and omics data. These data sets are extremely rich, but many legacy and home-grown informatics tools cannot handle their complexity and size. Silos, insufficient collaboration tools, and complex regulatory and security requirements can all hinder precision medicine programs. DNAnexus Apollo™, which supports precision drug discovery programs, empowers scientists and clinicians to analyze and explore omics and clinical data in a single environment built on a robust and scalable cloud platform. Apollo allows them to share data, tools and analyses securely with peers and colleagues from all over the world, regardless of whether they are on another floor or another continent.

We are a global provider for professional data storage solutions that are optimized for creative video, medical imaging and video surveillance. Our digital archive systems can store 100+ Petabytes of files and offer long-term, cost-effective, secure and long-term storage on RAID, LTO and optical cartridges. Our cloud solutions offer a global shared file system that makes your digital assets available to cloud computing and on-premises machines around the world.

BigOmics Analytics, a biodata analytics company, develops platforms that enable biologists to visualize and understand omics data. Omics Playground is our flagship product. It's a user-friendly software that helps users store and visualize data from experiments. BigOmics Analytics provides over 18 interactive modules and 150+ plots. This allows users to co-analyze with more than 6,500 public datasets. It also gives access to 50,000+ public pathways and gene sets. The platform integrates drug connectivity databases and drug sensitivity database with over 30,000 expression profiles. BigOmics Analytics is designed to help users discover more and spend less time on data analyses, all without the need for coding skills. The platform uses best-in class methods to ensure robust and reproducible results.

Comprehensive software for PET/CT/MR, PET/MR and nuclear medicine. Powered by world-class deformable registers and precise quantification tools. Mirada XD allows you to load unlimited multitime point follow up studies for your review, multitimepoint gated (4D), CT and PET data as well as multisequence MR or multi-phase CT data. In fused views, you can switch between MR sequences/gates at any time. You can perform efficient reading with unlimited and SPECT/CT studies. Data from a standalone NM SPECT scanner can also be fused to diagnostic CT. This eliminates the need for expensive equipment. Mirada XD allows you to perform efficient readings with unlimited SPECT or SPECT/CT studies. A standalone NM SPECT scanner can be used to fuse data with diagnostic CT without the need for expensive SPECT/CT equipment.

VIPER automates screening from remote patient identification (at point of diagnosis) through to qualified enrollment. VIPER uses artificial intelligence to match patients to precision trials within a narrow window of opportunity. This is done through the ingestion of lab-agnostic genomic and pathology data. It is tailored to the patient and the researcher. VIPER searches the personalized matching engine to locate the best clinical trials available for a patient's specific diagnosis--at that time. VIPER integrates workflow to send real-time notifications to the entire care team about a patient's eligibility in available clinical trials. This is done within a very limited enrollment window. VIPER provides interactive dashboards that allow you to access real-time data mining capabilities to aggregate patient data from both study and site levels to help you reach your study KPIs.

VSI HoloMedicine®, by apoQlar, is a software platform that uses the Microsoft HoloLens 2 hardware and transforms medical images, clinical workflows, and medical education into a 3D mixed-reality environment unlike anything else.

The QIAGEN CLC Geneomics Workbench is a powerful tool that works for all workflows. It is easy to overcome data analysis challenges with cutting-edge technology, unique features and algorithms that are widely used by scientists in industry and academia. Bioinformatics software solutions that are user-friendly allow for comprehensive analysis and interpretation of your NGS data. This includes de novo assembly and transcriptome assembly, resequencing analysis, WES and targeted panel support, variant calling, variant calling, RNA–seq, ChIP–seq and DNA methylation analysis (bisulfite sequence analysis). You can analyze your RNA-seq (miRNA, smallRNA) and smallRNA (lncRNA), data using easy-to-use transcriptomics workflows that allow for differential expression analysis at both gene and transcript levels. QIAGEN CLC Genomics Workbench was designed to support a wide variety of NGS bioinformatics programs.

Pathology Reporting Software ranks among the top Diagnostic Center Management Softwares in India. It can also be used as a Referral Laboratory Software. It can be used in both a network-based and stand-alone models. It can be used to bill diagnostic centers. It is the best pathology laboratory software. It simplifies your life with features like report generation, lab accounting, stock entries, and many more. Pathology Reporting Software is the most flexible data module for pathology labs. It can be used to disperse, record and compare data to all test performed in the lab. Pathology lab software can be integrated to centralize entire database and modules from clinics, diagnostic centers, medical laboratories, and pathological laboratories through a single interface. This framework allows you to access and maintain data such as billing, reports delivery, and many other information.

Concentriq, our AI-powered platform for software, sits at the intersection between digital and computational pathology. It connects functionality required to perform routine pathology operations with powerful AI applications to accelerate breakthroughs to improve patient outcomes. Laboratories around the world recognize the challenges we face today: a rising cancer burden and a shortage in pathologists. They also need to modernize quickly due to declining reimbursements and declining reimbursements. The time is right to grab this moment, as one billion pathology slides will be digitalized each year, creating vast amounts new data and information. Digital pathology gives today's forward-thinking pathology organisations the tools to overcome their collective challenges and fundamentally change how they work and contribute to medicine.

ACGIL offers pathology labs the flexible module for information that is used to record and disseminate data related to all laboratory tests. It allows users to receive online requests from doctors, and allows laboratory personnel create requests. It integrates pathology lab software to centralize all modules and databases of hospitals, clinics, and medical laboratories into a single interface. This system allows you to access and maintain information such as pre-booking, online receipts of requests, billing of tests and reports delivery, and many other functions. Our Clinical lab software makes it easy to keep records of all tests performed in the disciplines of Cytology/Hematology, Biochemistry and Neurology.

Geneyx Analysis provides a comprehensive solution to analyze next-generation sequencing data. It can be used by commercial and hospital labs. This advanced platform integrates AI and machine learning features to identify new biomedical insights while improving diagnostic yields. Geneyx Analysis provides a transparent and intuitive solution that allows clinicians and researchers complete control over their data analysis. This reduces the complexity of regulating internal bioinformatics workflows. Our comprehensive annotation engine can support the analysis of all genetic variations, including structural and copy-number variations, as well as regulatory components. Protocols can also be fully customized for gene panels, genomes, or exomes. Geneyx Analysis automates diagnostics from sequencer to report while creating a comprehensive resource of novel variants.

Store, archive, and manage multi-omic data sets. Illumina Connected Analytics provides a secure platform for genomic data to operationalize informatics, and drive scientific insight. CWL and Nextflow allow you to easily import, build and edit workflows. Leverage DRAGEN bioinformatics pipelines. Organize your data in a safe workspace and share it with the world in a compliant way. Our platform allows you to keep your data in the cloud. Visualize and interpret data using a flexible analysis tool, such as JupyterLab Notebooks. Data warehouses allow you to aggregate, query and analyze sample data and population data. Scale analysis operations through the creation, validation, automation, and deployment of informatics pipelines. Reduce the time needed to analyze genomic data when quick results are a key factor. Enable comprehensive profiling for the identification of novel drug targets and biomarkers of drug response. Data can be transferred seamlessly from Illumina sequencing platforms.

Genospace understands that genomics is driving precision medicine development, but scaling its delivery remains a challenge. We are here to help. Our platform makes biomedical data meaningful, accessible and easy to use for everyone, especially those at the frontlines of care delivery. Your clinicians and researchers will have the information they need in order to make informed decisions. Join us in our mission to leverage high-dimensional molecular data to improve patient outcomes and accelerate drug discovery and research. For drug development and research, large-scale population data is essential. Genospace platform allows you to conduct cohort-driven analyses that will inform your research activities. We are experts in clinical trial research. Genospace allows you to quickly accrue patients by matching fragmented patient data with complex trial criteria. The Genospace platform enables you to integrate genomic medicine into your mainstream clinical care.

Genoox is a growing and diverse community that gathers the most relevant data and delivers real-world genomic insights. These insights can be used to improve patient outcomes and shape the business of healthcare. Our solutions are changing genomics. Genoox leverages the power of its community to combine public data with community data to speed up the path from DNA sample through to clinical report. This improves patient care by making genomic information accessible and actionable at point of care. Genoox is a platform that enhances research and life science companies. It uses real-world data and evidence to power robust genomic analytics. This enables researchers to simplify complex genomic data and make important discoveries using the most advanced genetic tools. Genoox allows biosystems companies, such as DNA sequencing companies, to bundle their state-of-the art genomic engine with dedicated assays.

It is possible to quickly diagnose cancer accurately and affordably. One in three people will develop cancer during their lifetime. Cancer diagnosis can be slow and costly because doctors don't have the latest automated tools. Qritive is an AI-powered tool that allows doctors to analyse both microscopy images as well as text from patient data. Hospitals will be able to diagnose cancer more efficiently and save money by using Qritive. Pantheon, a CE-marked vendor-agnostic digital platform for pathology, enables digitization and rich report generation, and allows for AI analysis of whole-slide images. It can distinguish between benign and malignancies in breast tissue.

The toolkit was developed in the Data Sciences Platform of the Broad Institute. It offers a variety of tools, with a focus on variant detection and genotyping. Its powerful processing engine, high-performance computing capabilities and flexibility make it a great tool for any project. The GATK is a standard in the industry for identifying SNPs in RNAseq and germline DNA data. Its scope has now expanded to include somatic short variation calling, copy number (CNV), and structural variation (SV). The GATK includes not only the variant callers, but also many utilities that perform related tasks like processing and quality-control of high-throughput sequence data. It also bundles the Picard toolkit. These tools were designed primarily to process whole genomes and exomes generated by Illumina sequencing technology. However, they can be adapted for a variety other technologies and experimental design.

Partek bioinformatics software provides powerful visualization and statistical tools in an intuitive interface. Researchers of all levels can explore genomic data faster and more efficiently than ever before. We turn data into discovery®. Our intuitive interface makes it easy for scientists to perform sophisticated array and NGS analysis using pre-installed workflows. Public and custom statistical algorithms can be used together to quickly and accurately distill NGS data into biological insights. Genome browser, Venn diagrams and heat maps, as well as other interactive visualizations, show the biology of your next generation sequencing and array data in vivid color. Our Ph.D. scientists can be reached at any time to assist with your NGS analysis. This product is specifically designed for next-generation sequencing applications that require high-level computing. It offers flexible installation and management options.

Artificial Intelligence and RNA sequencing (RNA–seq data) are both a necessity and a way to develop therapeutics that target splicing mistakes. Machine learning allows us to quickly identify new splicing mistakes and design therapeutic compounds to correct them. SpliceCore, our AI platform for RNA therapeutics research, is what we call SpliceCore. This technology platform was specifically designed for the analysis and interpretation of RNA sequencing data. It can identify, validate and test hypothetical drug targets quicker than traditional methods. Our proprietary database of over 5 million potential RNA-splicing errors is the heart of SpliceCore. It is the world's largest database of splicing mistakes and is used to test all RNA sequencing data that is submitted for analysis. Scalable cloud computing allows us to process large amounts of RNA sequencing data efficiently at a higher speed and lower cost, thereby exponentially accelerating therapeutic innovation.

Combining the multiomic data and medical history of an individual to deliver more personalized healthcare. Use purpose-built databases to support large-scale analyses and collaborative research across populations. Accelerate your research with scalable workflows, integrated computation tools and integrated computing. Protect patient privacy by ensuring HIPAA compliance and using built-in data access, logging and logging. AWS HealthOmics enables healthcare and life sciences organizations and their software partner to store, query and analyze genomic, transcriptionomic, or other omics data, and then generate insights using that data. Store and analyze omics for hundreds of thousands patients to understand the relationship between omics variation and phenotypes in a population. Create reproducible and traceable workflows for clinical multiomics to reduce turnaround time and increase productivity. Integrate multiomic analyses into clinical trials to test out new drug candidates.

DNAnexus Titan™, a trusted data analysis solution, is the future of genomics and clinical pipelines. Legacy informatics tools are not designed to handle today's larger volumes of sequencing data. Research centers and clinical diagnostic test companies find it difficult to create, refine and validate pipelines using home-grown systems. DNAnexus Titan™ is a unified platform which removes bottlenecks from development and production. It brings all data and pipelines into one place, resulting in unparalleled efficiency. Let us handle the heavy lifting in managing industry- and region-specific compliance and security requirements, while meeting the global demand for sequencing information.

The award-winning XIFIN LIS, a SaaS-based laboratory information platform, is fully scalable and scalable. It offers flexible and secure connectivity, multi-specialty workflows and cutting-edge capabilities to optimize complex and high volume testing labs. The healthcare industry is changing to accommodate patient-centered and value-based coordinated care models. The rapid adoption of next-generation sequencing (NGS) and genomic testing is accelerating this shift. Laboratories will need to adapt their processes to meet the challenges of reporting and implementing these complex tests. Diagnostic insights can help reduce healthcare costs and improve patient care. It is therefore crucial that laboratories integrate better with the healthcare system. These demands drive greater interaction and communication among all healthcare and diagnostic providers.

A stack of distributed and decentralized technologies that is both enterprise-ready and developer-friendly. ProximaX Sirius is a platform that consists of multiple servers distributed across a network. It is a "hub-and-spoke" design. The core component of the platform is the blockchain or the "hub", and the other components, or the "spokes", are the service layers or "spokes". The service layers include P2P and distributed storage as well as streaming, database, and supercontract. All storage, messaging and transactions are encrypted. Streaming can be used to stream text, video, or voice data. ProximaX Sirius can offer additional service layers to provide more functionality. These layers can be anything, from specialized services like artificial intelligence to distributed computing for gene sequencing. However, performance of individual layers is not affected by the expansion of service levels. This is similar to multiple networks server nodes running simultaneously and linked together by the blockchain core.

Our healthcare-specific Natural Language Processing and AI Engine stores more than 70% of healthcare data in clinical documents, reports and patient charts, clinician notes, discharge letters, and patient charts. This allows us to identify the concepts, attributes, and context that are needed to deliver business insight, optimize billing, identify and rank patient risks, compute quality metrics, collect sentiment and outcome data, and provide business insights.

Correlation Engine, an interactive omics database, places private omics data into a biological context by combining it with highly curated publicly available data. Correlation Engine, one of the largest databases in the world for life science research, provides researchers with unprecedented access and insight to a vast number of high-quality whole genome analyses. The knowledgebase allows for novel discoveries through the interrogation of billions of datapoints derived from standard analyses of whole genome studies. A suite of applications for determining biological context, a constantly growing library of curated datasets, and support of multiple species and multi-omic data sets. Use a simple graphical interface to leverage guided workflows and APIs. Accelerate the journey from omic to decision-making and gain access to more than 25,000 multi-omics studies that have been reanalyzed (from over 250.000 signatures).

Automated surveillance of any source of data, fully integrated with a GVP IX-compliant signal management platform. GVP-IX compliant signal-management platform integrated into Evidex and ready-to-use off-the-shelf. Modernize and audit-proof all your management processes without the need to switch between platforms or services. Your safety data is worth more than you think. Automating signal detection and management allows you to focus on your organization's value, not just regulatory requirements. Safety signals can be identified from traditional sources such as ICSR databases, FDA Adverse Events Reporting System (FAERS), VigiBase, and clinical trial data. Incorporate new data sources like claims, EHR, or other unstructured data. These data sources can be combined seamlessly to improve signaling algorithms, increase validations and assessment efficiency, and provide faster answers for drug safety questions.

3decision®, a cloud-based repository of protein structures, is designed to manage structural data and perform advanced analytics. This allows small molecule and biologicals discovery teams the ability to accelerate structure-based drugs design. It centralizes, standardizes, and integrates experimental and in silico protein structures derived from public sources such as RCSB PDB, AlphaFoldDB as well as proprietary information, including formats like PDBx/mmCIF, and ModelCIF. This allows for easy access to X-Rays, NMRs, cryo-EMs, and modeled protein structures. It also fosters collaboration and enhances research efforts. 3decision®, beyond storage, enriches entries by adding metadata and sequence data, including annotations of antibodies, binding site details, and protein-ligand interaction. Advanced analytical tools can identify druggable site, assess off-target risk, and enable binding sites comparisons. They transform vast structural data into actionable information. Cloud-based platform allows for collaboration between research teams.

Cellenics can help you turn your single-cell sequencing data into meaningful insights. Cellenics is an open-source analytics tool developed by Harvard Medical School for single cell RNA sequencing data. Biomage hosts the community instance. It allows biologists to explore datasets of single-cells without having to write code, and helps scientists and informaticians work together more effectively. It can take you from count matrixes to publication ready figures in a matter of hours. It can also be seamlessly integrated into your workflow. It is fast, interactive and user-friendly. It's cloud-based and scalable. Cellenics, hosted by Biomage as a community instance, is free for academics with small/medium datasets (upto 500,000 cells). Over 3000 academic researchers use it to study cancer, cardiovascular health and developmental biology.

AWS HealthImaging was designed for developers who create cloud-native applications for medical imaging. HealthImaging ingests DICOM P10 data and provides APIs to retrieve and store it with low latency. By using advanced compression and storing only one copy of each image, you can reduce costs by up to 40%. Cloud-native APIs, applications and APIs allow you to access medical imaging data from anywhere with a subsecond latency. Reduce the burden of managing infrastructure to focus on providing high-quality patient healthcare. Major medical imaging vendors support cloud-native workflows for medical imaging. Store and stream medical images directly from AWS, while maintaining low-latency performance. Save money on long-term archiving while maintaining access to images in subseconds. With the help of other tools and services, run artificial intelligence and machine-learning inferences over the imaging archives.

Interactive visualizations and analytics allow you to explore hundreds of single-cell transcriptome datasets as well as your own data. The software supports multimodal omics (e.g. CITE-seq and spatial transcriptomic. Explore the world's largest database of single-cell expression interactively. Access and query insights derived from a single cell database of millions of cells. The database is fully annotated, with cell type labels and experimental meta-data. BBrowser does not just create a portal to published works. It is an end-toend solution for YOUR single-cell data. Import your fastq, count matrices or Seurat objects and reveal the biological stories within. With a powerful package of visualizations, analyses and an intuitive interface you can easily mine insights from any single-cell dataset. Import data from single-cell CRISPR or Perturb-seq. Guide RNA sequences can be queried.

Deeplink Medical developed its offering around the MIRIO platform. This adapts to the various use cases and needs for actors involved in medical image in oncology, in clinics, and in routine. Our services are based on three complementary offerings, MIRIO, which is a platform for the monitoring of solid tumors and the treatment response of patients in oncology. The patient pathway is a link between hospitals and liberal medicine. An Imaging CRO is responsible for the monitoring of imaging data during oncological clinical trials. Our solutions are supported by a scientific board. A collaborative workflow platform that structures imaging data and radiological examinations for patients suffering from solid tumors. This allows structuration of data in real time (according to the RECIST 1.1 or iRECIST) at the initial creation of the data. Real-time evaluation of treatment response according to international guidelines RECIST.1.1 and iRECIST.

High-quality medical image management in a HIPAA-compliant environment. Mirror PhotoFile is the backbone of medical image capture systems. It features the industry-standard Mirror medical interface and patient chart structure. Mirror PhotoFile makes your medical images immediately accessible and provides HIPAA security features. Mirror software is used by hospitals for medical image management. Mirror consultation app for iPad®, combines powerful image-based patient communications with tablet convenience. Access your entire Mirror client database and data from anywhere within the facility. Ensure that your clients are connected while you discuss the options for aesthetic treatments. Clients can access a secure, password protected web portal to view their photos, treatment recommendations, and track the progress of treatments from the comfort of their own homes.

Disks from outside organizations are flooding hospitals and imaging centers. Manual import of data can be very time-consuming and costly. Automated Disc Importer allows organizations to import large volumes of discs into local or temporary cloud storage. This automates the process and eliminates the need for human intervention. After discs have been read, users can reconcile the data and then import it into their archive. The Automated Disc Importer takes a photo of each disc label being read to provide additional security. The photo clearly identifies the disc's origin. Automated Disc Importer ingests reports and medical images from DICOM discs. This drastically reduces the time required for manual importing.

Choose two custom cell groups and compare their top differentially-expressed genes. Use millions of cells in the integrated CZ CELLxGENE Corpus for powerful analyses. Use an interactive, no-code interface to perform interactive analyses of a dataset. Explore how spatial, environmental and genetic factors influence gene expression patterns. Use published datasets to understand them or as a starting point for identifying new cell subtypes and states. Census allows you to access any custom slice of standard cell data from CZ CELLxGENE in R or Python. Explore an interactive encyclopedia that contains 700+ cell types, detailed definitions, markers genes, lineage and relevant datasets. Browse and download 1,000+ datasets and hundreds of standardized data sets that characterize the functionality of healthy human and mouse tissues.

A global, infinitely scalable, AI powered, collaborative cloud platform that is globally accessible and meets the highest standards for security and compliance. A leading, easy-to-use platform for neuroscience professionals. It was designed by data scientists and neuroimaging experts to meet the unique and challenging needs of the community. Optimized for your specific needs, whether you are conducting clinical trials, designing new algorithms, or leveraging brain-related data.

The Acuo VNA image management system consolidates all imaging information within an enterprise into one repository. This allows for seamless communication with core information technology systems like the EMR. The Acuo VNA gives healthcare organizations true ownership of all non-DICOM and DICOM imaging information through standard data formatting. Your imaging platform with Acuo healthcare software is highly scalable, flexible, and ready for change. Acuo's multi-tiered VNA Database Architecture keeps a complete history of image ownership. This allows images to move easily with hospitals through mergers, acquisitions, and new business models. Acuo is one VNA that supports this capability, allowing you to have centralized image management and still support individual department workflows and data-ownership. Flexible deployment options, including hybrid, cloud, and on-site.

Software for fast, simple, and repeatable analysis of variants in gene panels, whole genomes, and exomes. VarSeq provides an intuitive and integrated software solution for tertiary analyses. VarSeq allows you to automate workflows and analyze variations for gene panels, whole genomes, and exomes. Our software makes it easier than ever to understand genomic data. VarSeq is a powerful software that provides a powerful filtering engine and annotation engine for sifting through large variant data. You can narrow down your list of variants quickly by using a series of filters. You can save the filters you have created after you have determined the parameters that are most effective for your analysis. This allows you to easily apply the same analysis on another dataset. VarSeq is ideal for high-throughput environments because the same automated workflow can apply to each batch of samples. Real-time filtering allows you to quickly prototype and fine-tune analysis workflows.

Improve efficiency and empower your team with the knowledge to make intelligent decisions about IT operations and patient outcomes. Seamless data integrations and highest data security standards enable data access from any location or device. Eliminate legacy tools and multiple vendors in order to unlock the cost savings and efficiency gains that come with a system-wide unified imaging network. Silverback becomes smarter, faster, and stronger with each data interaction. Over time, the engine tracks and identifies patterns to deliver predictive insight throughout the image network. Vue, the dynamic DICOM router at the core of the Silverback platform distributes studies intelligently throughout the enterprise. The router orchestrates images across multiple sites and vendors using customized logic rules. Vue can be placed in front or behind the PACS to capture, manage and distribute studies across the network.

AES Medical's PathoSys®, cellular pathology reporting software, was developed in partnership with consultant pathologists. It was the first to receive recognition by the Royal College of Pathologists. The system incorporates the Royal College of Pathologists data. It provides standard reporting and structured data capture, which facilitates rapid real-time audits and export of structured pathology data. Laboratory system integration - eliminates double entry of report and demographic data while distributing reports. Pathology Network was designed from the ground up to provide support for multiple laboratories, facilitating network-wide audit and reporting. It is easy to use, quick real-time search and audit reverse the (90%/10%) balance in workload to gather data instead of analyzing it for clinical audit.

GenomeStudio Software allows you to visualize and analyze data from Illumina array platforms. This powerful tool supports genotyping analysis of microarray datasets. Performance-optimized tools and a user-friendly graphical interface enable you to convert data into meaningful results quickly and easily. Analyze SNP/CNV data across 5,000,000 probes and markers. Detect outliers in sample data. Analyze differentially expressed genes across multiple genomes. Profile miRNA expression. Combine microRNA and mRNA data into one project. Single-base resolution detection of cytosine methylation. Identify methylation signatures throughout the entire genome. Illumina's goal is to use innovative technologies to analyze genetic variation and function. This will allow us to do studies that were impossible just a few short years ago. We believe it is vital to provide innovative, flexible, and scalable solutions that meet the needs of customers.

Galaxy is a web-based, open-source platform for data-intensive biomedical studies. Start here if you are a new Galaxy user or consult our support resources. Install Galaxy yourself by following the tutorial. You can choose from thousands of tools in the tool shed. This instance of Galaxy uses infrastructure generously provided to it by the Texas Advanced Computing Center. Additional resources are available primarily via the Jetstream2 cloud, via ACCESS and with support from National Science Foundation. Quantify, visualize and summarize mismatches from deep sequencing data. Build maximum-likelihood trees. Phylogenomic/evolutionary tree construction from multiple sequences. Using TN-93, combine matching reads to form clusters. Remove sequences that are within a certain distance of a cluster from a reference. Estimate gene essentiality scores using maximum-likelihood.

Color offers one the most accessible and clinical-grade genetic tests available today. It analyzes genes associated with cancer risk and heart conditions, as well as how the body processes certain medications. We offer a range of services, tools and expertise to help you recruit new patients and engage them in care journeys that are relevant to them. We take a comprehensive view of the patient's health, including genetics, family history, lifestyle and behavior, and personal health information, to recommend specific solutions or care based on personal risks.

AIDDISON™, a drug discovery software, combines the power and efficiency of artificial intelligence (AI), computer-aided design (CADD), and machine learning (ML) to provide a valuable toolkit that can be used for medicinal chemistry. It is a unified platform that integrates all aspects of virtual screening, including ligand-based design and structure-based design. It also supports methods for in silico lead optimization and discovery.

Aiforia provides powerful cloud-based technology and deep learning to assist pathologists and scientists in clinical and preclinical labs. This allows them to improve their image analysis tasks. Aiforia's expertise and experience can transform healthcare from diagnosis to treatment. It can help researchers identify novel biomarkers of disease and support R&D scientists in speeding the time-to market of new drugs. Aiforia Clinical Suites are a suite of tools that can be used to improve the productivity and accuracy of clinical pathology labs. We are currently working on Suites for some the most common cancers in the world and have CE-IVD marking to mark AI models in breast and lung cancer.