Alternatives to Luna

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.

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.

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.

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.

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.

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).

DHI-Plus software helps dairy managers improve herd productivity and clarity by focusing on the cows that require attention. This includes vet actions, production SCC, breeding, treatment, genetic values, and more. Recording health data is essential now more than ever, especially with the addition of genomic evaluations and health data. Your operation will thrive if you use that data to make informed decisions. You can manage the animal's well-being. Keep track of health data to improve your herd's future. Protect your business and comply with FDA requirements. The Drug Tracking Module (DHI-Plus) software is ideal for maintaining FDA regulatory compliance. It can also be used to improve or enhance herd health, resulting in better milk yield. With mobile options, you can even record cow-side treatments. To meet compliance standards, record and track treatments.

Vytelle is a precision livestock business that reshapes the way cattle producers around the world optimize their herds. Our solutions reduce uncertainty and help you make the most important decisions regarding reproduction and mating. Vytelle™, our proprietary individual animal data capture software, is VytelleSENSE™. It records feed intake and inpen weight gain to help you identify high-performing animals that exhibit important economic and environmental traits. Low-contact devices capture key performance data without stressing the animal and communicate it to other information for processing and integration. Our decision tools are powered by the only AI analytic engine in the industry, based on 30 years of continuous improvement in helping producers collect and use data about cattle. It quickly processes phenotypic and genomic data, as well as performance data, to create easy-to-read dashboards, reports, and reports that allow you to make better decisions for your cattle operation.

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.

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.

Aspect Analytics is a multi-omics spatial platform for collaborative cross-disciplinary data management and analysis. For teams working in drug development, biomarker research, pathology analysis and beyond. Aspect Analytics facilitates cross-disciplinary collaboration and enables breakthrough research by bringing multi omics data into one collaborative platform. Add different spatial omics measurements to one visualization simultaneously. Our platform will combine data from all of your spatial multi-omics tests to give you the insights you require. Securely store and manage petabytes. Access it anywhere, anytime. Scale and customize your data infrastructure to meet your needs. Integrate spatial biology data across different technologies and vendors, regardless of data format. Set up automated workflows to run in-depth analysis on large datasets in parallel.

OmicsBox, a leading bioinformatics tool, offers end-toend data analysis for genomes, transcriptomes and metagenomes. It also provides genetic variation studies. The application, which is used by leading private and public research institutes worldwide, allows researchers to process large and complicated data sets and streamline their analytical process. It is designed to be efficient, user-friendly and equipped with powerful tools to extract biological insight from omics data. The software is divided into modules, each of which has a set of tools and features designed to perform specific types of analyses, such as de novo genome assemblies, genetic variations analysis, differential expression analyses, taxonomic classifications, and taxonomic classes of microbiome, including the interpretation of results and rich visualizations. The functional analysis module uses the popular Blast2GO annotating methodology, making OmicsBox a great tool for non-model organisms research.

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.

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.

Mosio allows research teams to improve subject adhesion, communications, data collection, and communication on mobile's most popular channel, text messaging. Our software helps research teams communicate more efficiently with participants by delivering interactive elements to mobile phones and messaging automation. WHO CAN WE HELP? + Clinical Trial Sponsors (Pharma & Biotech) + Cancer Centers and Clinical Research Organizations + NIH-Funded Studies + Public Health Agencies + Clinical Trial Managers/Directors and Clinical Operations Managers/Directors. Clinical Project Managers. Principal Investigators. Clinical Research (Study). Coordinators. All research staff who regularly communicate with study participants. BENEFITS + Interactive medication reminders and medication compliance alerts + Automate data collection. + Increase engagement and adherence. + Get SMS appointment reminders to fix your no-show problem. + Increase retention with automated check ins

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.

All researchers from different industries can use the same environment! ResearchManager is a platform that allows researchers to access all functions and information from one place. They can also share it with others. This platform is for researchers who are ready for the future. Future where patient and data access and sharing are central. We provide support for everyone involved in research in the life sciences sector. This is done through an online platform that includes the eClinical tools EDC and CTMS & ERMS. This allows researchers to share data and facilitates research at a higher level. We are also experts in the fields of data validation, enrichment, and collection.

Our global data-sharing networks generate clinically actionable insights to improve patient outcomes globally. SOPHiA GENETICS is on a mission to build the future in AI-assisted medical care. We are integrating multimodal data from healthcare-omics, unlocking existing data silos and developing machine learning models in order to produce actionable insight that can eventually support healthcare professionals improve patient outcomes. The new interface, features, and cutting edge capabilities will accelerate precision medicine workflows and bring us closer to democratizing the data-driven medicine.

The Bioconductor Project aims to develop open source software that allows for repeatable and precise analysis of biological data. We encourage a collaborative and inclusive community of data scientists and developers. Resources to maximize Bioconductor's potential. Our tutorials, guides, documentation, and guides cover everything from basic functionality to advanced features. Bioconductor is an open-source and open-development software that uses the R statistical language. It has an active user base and two releases per year. Bioconductor offers Docker images with every release, and supports Bioconductor in AnVIL. Bioconductor, founded in 2001, is an open-source project widely used in bioinformatics. Over 1,000 developers have contributed over 2,000 R packages, which are downloaded over 40 million times per year. Bioconductor is cited in over 60,000 scientific publications.

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.

Our cutting-edge platform, the Medidata Clinical Cloud, transforms clinical trial experiences for patients, sponsors and CROs. The Medidata Clinical Cloud is the only unified technology platform that focuses exclusively on clinical research. It addresses every step of the research process, from start to finish. Our platform helps medical device and life science organizations reduce development costs, minimize risks, and bring treatments and devices to market quicker. The Medidata Clinical Cloud will allow you to access the power of any product you choose for your clinical trials program. Medidata is leading the digital transformation in clinical research. Our platform, powered by artificial intelligence, machine-learning, advanced analytics, and advanced research, brings together researchers, study managers and investigators to accelerate research. Obtain regulatory-compliant, patient-friendly electronic informed consent for clinical trials.

Accelerating the development and delivery of life-saving medicines, and enabling cancer patients to have access to the best quality of cancer research and care. Our software revolutionizes patient access to innovative drugs & clinical trials. FICS is a software that allows the collection of regulatory standards data during patient care. FICS combines traditionally separate and noncommunicating applications to create a novel end-to-end platform. This allows clinical trials to be performed faster, easier and with greater quality.

Founded in order to improve lives through high-value care, the hc1 platform has become a leader in bioinformatics for precision prescribing and testing. The cloud-based hc1 high-value care platform® organizes large amounts of live data, including genomics and medications, to provide solutions that ensure the right patient receives the right test and prescription. The hc1 Platform is a platform that powers solutions that optimize diagnostic testing, prescribing, and patient care for millions of patients across the country. Visit www.hc1.com to learn more about the proven approach of hc1 to personalizing care and eliminating waste for thousands upon thousands of health systems, diagnostic labs, and health plans.

Choose Curebase to conduct your next study. You will experience more diversity, better enrollment, and better retention. Our innovative approach allows patients to participate at their own homes and with community doctors, resulting in faster, more cost-effective, and more diverse studies. Curebase offers a unique combination: Curebase has in-house virtual CRCs, paired with a global network virtual PIs working with community doctors to bring studies anywhere. Patients don't usually live near traditional research sites. Our trials bring the research into patients' homes, as well as real-world medical settings such community doctors' offices. Patients enrolled in Curebase infectious diseases trials were successful thanks to a new model that meets patients at their location through virtual and community healthcare.

We help healthcare systems reduce their burden by providing automated analysis, diagnosis and treatment solutions to healthcare professionals and patients around the world. Congenica was founded by pioneering work done at the Wellcome Sanger Institute in the UK and the NHS. Our products combine the latest technology, automation and AI to create a platform that is uniquely differentiating. This platform can be used in any area of human disease, where genomic data is critical to unlocking actionable insight. We are a digital healthcare company that provides software and solutions to analyze and interpret genomic data at large scale. Full automation using powerful APIs and ML, to reduce the burden of specialist staff, increase case throughput, speed up decision-making and streamline reporting. Platform for accurate, certified, and secure clinical decision support with the highest level of confidence in clinical outcome.

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.

Software that acquires, learns, and grows customers to maximize growth with mathematical certainty. Machine learning and marketing automation make predictive marketing easier, more efficient, and more enjoyable for customers both online and offline. BuyerGenomics is more than a legacy ESP, CDP or CRM. It has become the Predictive Marketing Automation tool of choice for modern retail marketing professionals. It is crucial to organize and capture customer data. BuyerGenomics constantly updates its 360-degree, multichannel customer profile. BG adapts the content and timing of marketing to provide the best experience for customers. BuyerGenomics converts the insights it has on customers into action and revenue, but it also produces meaningful analytics that will inform your marketing strategy.

g.nome is a cloud-native, workflow-optimized platform that provides streamlined, scalable and interoperable workflows to perform next-generation sequencing analyses. g.nome offers a low-code/no code pipeline build. Using pre-built toolkits and workflows from a curated collection, g.nome gives researchers the power to import custom code and handle large datasets reliably. With g.nome you can remove long-standing barriers related to workflow language, visibility of process flow, and quality control. All that's left is streamlined, interoperable, and scalable genomic workflows. This allows research teams to focus on what they do best, which is the science.

IQVIA is trusted by thousands of organizations worldwide to accelerate drug development, improve product quality and safety and commercial effectiveness, get the right treatments for patients, improve healthcare delivery and access, and ultimately drive better outcomes. Connect data, technology and analytics to optimize clinical development. The result? The result? Faster decision making and lower risk, so you can deliver life-changing treatments faster. IQVIA offers specialized capabilities to customers in the healthcare industry, thanks to its foundation in data, advanced analytics and expert insights. Watch the latest from IQVIA data scientists and doctors, as well as other subject matter experts, on the topics that are important to you. You can find everything you need, from industry trends to how our capabilities are being applied to help, here.

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.

Mednet is an eClinical technology company that specializes in healthcare solutions for the global life science community. Mednet's flexible, EDC-centric eClinical platform increases the efficiency of clinical research of all sizes. Mednet's comprehensive solution suite provides all the tools necessary to create and manage clinical research. It can also adapt to changing demands and requirements. Mednet has been trusted by CROs in every sector of the pharmaceutical, medical device, and biotechnology industries for almost 20 years. They provide the expertise, reliability, and innovation that they need to succeed. Mednetsolutions.com has more information.

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.

Deep 6 AI disrupts clinical trial enrollment by changing the way researchers identify eligible patient. DEEP 6 AI uses artificial intelligence and natural-language processing to mine structured and unstructed patient data. This allows DEEP 6 AI to find more patients that are better-matched for trials in a matter of minutes, rather than months. Deep 6 AI is used by some of the most prestigious health systems, pharmaceutical companies, and CROs around the globe. This makes the DEEP 6 platform an essential step in their clinical research workflow, greatly speeding up patients' access to clinical trial. Deep 6 AI locates more patients for clinical trials than it takes months. This allows people to receive life-saving treatments much faster. Deep 6 AI analyzes both structured data such as ICD-10 codes and unstructured clinical information, including doctor's notes and pathology reports. It also provides free-text access to important medical data that cannot be searched easily.

Alissa Interpret provides a universal software solution for the interpretation of genomic data in clinical decision support. Alissa Interpret is a platform that can be used for CGH or NGS tertiary analyses. It will increase your productivity, reduce turnaround time and maintain regulatory compliance. Alissa interpret, Agilent's SureSelect NGS reagents and intuitive Alissa Reporter for secondary NGS analysis, Magnis walkaway automated, and TapeStation QC will help you achieve complete operational efficiency. You can access external and internal variant knowledgebases. Automated variant analysis solution accelerates CGH/NGS tertiary analyses. SNVs and InDels are all handled by the same platform. CNVs, LOHs, fusions, CNVs and InDels can also be analyzed. Integrate with your LIMS to eliminate bottlenecks in genomic data analysis. Connect with peers to share knowledge and improve diagnostic yield.

OpenText™, a leading provider of information management solutions for life sciences organizations, helps them to harness insights from data and content to improve their decision-making and accelerate product development. Integrate, manage and securely exchange data between people, systems, and things. Use information assets to drive innovation and commercialization. Cloud-native software can run anywhere, giving you freedom of choice. OpenText for life sciences accelerates discovery by delivering actionable insights that can be used to drive innovation in pipelines. Intelligent capture allows you to capture and manage research papers in electronic lab notebooks. Text mining can help you gain insights. Unstructured text in clinical trial reports, study protocol, clinical safety and efficiency findings, can be used to extract knowledge. Learn how to intelligently analyze and classify clinical trial documents and extract them to reduce the risk for costly stops and starts.

JADBio is an automated machine learning platform that uses JADBio's state-of-the art technology without any programming. It solves many open problems in machine-learning with its innovative algorithms. It is easy to use and can perform sophisticated and accurate machine learning analyses, even if you don't know any math, statistics or coding. It was specifically designed for life science data, particularly molecular data. It can handle the unique molecular data issues such as low sample sizes and high numbers of measured quantities, which could reach into the millions. It is essential for life scientists to identify the biomarkers and features that are predictive and important. They also need to know their roles and how they can help them understand the molecular mechanisms. Knowledge discovery is often more important that a predictive model. JADBio focuses on feature selection, and its interpretation.

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.

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 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.

Clarity LIMS, a laboratory information system, is designed for genomics laboratories to track samples and manage workflows in order to optimize and efficiently run the lab. Clarity LIMS is capable of much more than just tracking samples. It is the digital backbone for your lab and actively manages all laboratory operations from sample and data collection to people, instruments and consumables. Clarity LIMS automates and standardizes workflows to save time and reduce the risk of human error. It can be scaled to fit your laboratory ecosystem and accommodate new technologies. Clarity LIMS is a laboratory information management system. Pre-packaged workflows, Illumina sample/library preparation kits and instruments and quality control features flagging poor-quality samples help your laboratory save time. Supports compliance with eSignatures, audit trails, reagent tracking and lot tracking and privacy and security controls Automated business logic and error checking promote accuracy

ESMFold demonstrates how AI can provide new tools for understanding the natural world. It is similar to the microscope which allowed us to see the world at a tiny scale and gave us a new understanding of the world. AI can help us see biology in a different way and understand the vastness of nature. AI research has largely focused on helping computers understand the world in a similar way to humans. The language of proteins is a language that is beyond human comprehension. Even the most powerful computational tools have failed to understand it. AI has the potential of opening up this language to our comprehension. AI can be studied in new domains like biology to gain a better understanding of artificial intelligence. Our research reveals connections across domains. Large language models that are behind machine translation, natural speech understanding, speech recognition, image generation, and machine translation are also able learn deep information about biology.

EvidentIQ's eCOA optimizes real-time, direct from-patient data collection. It offers a simple interface that provides advanced patient assessments to improve the patient experience and data quality. Customers can either benefit from an entire eCOA package, or choose the elements that meet their specific needs to create value. Get a demo from our experts to see how we can help you improve your study ROI. EvidentIQ's eCOA brings together data science and technology. Customers can either benefit from an entire eCOA package that covers all aspects of the process or add value by choosing elements that meet specific requirements. The solution can be used independently of any specific eClinical technologies, such as EDC systems. However, it can be integrated into any existing eClinical software. It has been created to collect any patient/clinician/observer reported outcome data in a streamlined, compliant and efficient way.

LexisNexis Health Equity and Inclusion Insights provides comprehensive and actionable data at the individual level on social drivers of healthcare (SDoH). The insights allow healthcare organizations to advance initiatives in population health, health equity, and clinical research. The solution helps identify barriers in care, improve the delivery of care, and create more diverse clinical research and healthcare options. It provides deidentified datasets which can be combined with another deidentified dataset using LexisNexis Gravitas. This tokenization solution leverages a referential layer to match deidentified records with unprecedented precision. To achieve these goals and improve health equity, it is important to identify barriers to health and predictors for poor health outcomes. This will allow targeted action that can make a difference to each patient.

Improve team productivity and generate greater returns on research. Interactive data visualization allows you to share private and public data with other teams. Rosalind is a multi-tenant SaaS designed for scientists. Analyze, share, interpret, plan, validate and generate new hypotheses. Code-free visualization, AI-powered interpretation, best-in-class collaboration. ROSALIND is suitable for scientists of all levels, since it does not require any programming or bioinformatics knowledge. ROSALIND's powerful downstream analysis and collaborative capabilities make it a platform for discovery and data hub that connects experiment design, quality assurance, and pathway exploration. ROSALIND manages tens or thousands of cores of computing and petabytes in storage to dynamically scale each experiment up and down to deliver results. Share results instantly with other scientists around the world with audit tracking, so everyone can concentrate on interpretation and not the processing.

All your business's reopening can be managed from one dashboard. Passport is a secure, customizable dashboard and app that helps employers and communities to navigate their return to the workplace. Follow the CDC guidelines and then create specific rules for each work location. The app generates a digital badge for employees when they check in. It's valid for 24 hour. You can track your employees' status by checking in on badge check-ins. Your employees can download Passport and fill out their health survey declaration to get started. The app generates a QR code that is time-limited and cryptographically signed. Your dashboard can be configured in minutes to manage your community or workforce without any IT management or integrations. Passport, as all doc.ai products is, is designed to protect all users' privacy. Passport securely stores personal information such as health symptoms on the user's phone.

Clinical Conductor CTMS (Clinical Trial Management System) is a cutting-edge system for managing clinical trials. It's suitable for hospitals, research sites and asset management companies. Site networks, health systems, contract research organizations (CROs), and other healthcare facilities. This cloud-based solution makes clinical trials more efficient and helps research organizations make better business decisions. The key features include electronic data capture and enrollment management, document management, recruitment management, and many more.

High-quality ePRO/eClinRO can unlock more evidence. Electronic Clinical Outcome Assessments (eCOA) measure how patients feel and function during clinical trials. By capturing clinical data electronically, you can be confident that your patient's data is high-quality and regulatory-compliant. eCOA eliminates the time and quality issues that paper diaries can cause, such as illegible answers and transcription errors, inconsistent or conflicting data, and saves you both time and money. ePRO is also recommended by the FDA. Patients can report on their health using questionnaires or assessments. Examples include activity outcomes or quality of life. The outcomes were reported by the clinician. A clinician reports health outcomes. A physical exam such as PASI is an example. Performance outcomes are measures of the patient's performance in completing specific tasks. One example is performing a timed task.

Research and clinical trials were traditionally conducted outside of local hospitals and doctors' offices. Patients didn't know that research could improve their health or their outcome, and doctors weren't always informed. Elligo allows for a wider participation in clinical research. With access to more than 150 million patients and their data (and more than 150 million others), physicians can offer research as an option to patients who otherwise wouldn’t have access. Traditional methods of recruiting are limited by geographical limitations, such as the proximity of patients to research sites. Patients prefer to work with their trusted healthcare provider.

Collaboration and document control. myClin is an eTMF platform that allows for collaboration and collaboration. You can upload and share your study documents on myClin's secure central channels. You can access your documents quickly and receive critical updates and training faster. You have full control of your data. The "File it!" feature allows you to see who has read and understood your study materials. You can record evidence of study execution and review training actions such as views, filing or downloading at individual or team level. Inspection readiness. Always be ready for inspection. Our compliance score shows how compliant each study site or team member is with the appropriate study information. You will be guided to areas that are less compliant in your study. This helps you improve risk management. We will create a myClin channel so you can share myClin with the team in just a few hours. It's that simple.

PicnicHealth brings together patients and researchers to provide the most accurate, relevant real-world data. We can create the most comprehensive picture of patient health by working directly with patients, and not just one specialist or care site. With our established patient communities and quick recruitment through dozens if not hundreds of established direct-to patients channels, it is easy to build the right patient cohort. Patients can sign up in just 10 minutes and gain access to their medical records. Are you a part of ongoing trials or registries for patients? PicnicHealth will help you set them up. Our platform provides real-world data tailored to each patient. You can specify the data elements you want to extract from medical records. This includes narrative text, doctors' notes, and more. Patients can contribute more with our unique patient-centric approach to real world data.