Alternatives to Jinni

Qloo, the "Cultural AI", is capable of decoding and forecasting consumer tastes around the world. Privacy-first API that predicts global consumer preferences, catalogs hundreds of million of cultural entities, and is privacy-first. Our API provides contextualized personalization and insight based on deep understanding of consumer behavior. We have access to more than 575,000,000 people, places, and things. Our technology allows you to see beyond trends and discover the connections that underlie people's tastes in their world. Our vast library includes entities such as brands, music, film and fashion. We also have information about notable people. Results are delivered in milliseconds. They can be weighted with factors like regionalization and real time popularity. Companies who want to use best-in-class data to enhance their customer experiences. Our flagship recommendation API provides results based on demographics and preferences, cultural entities, metadata, geolocational factors, and metadata.

Luigi's Box is a unique technological solution that uses AI to bring customers only relevant search results and personalized product suggestions, enhances the user experience, and unlocks the potential of your business. It is a year-by-year awarded easy-to-operate solution with a support team that acts in the interest of your continuous success. Luigi's Box offers easy no-code self-service integration - you only need to paste the tracking script into the header of your web. But there is more; we understand that every platform has different needs and preferences, and therefore we offer several more integration options to choose from. Luigi's Box offers several advanced features to increase search relevance and revenue and avoid fruitless searches and other unnecessary troubles, which reached out and helped companies such as O2, Mountfield, and Dr.Max. These use cases are proof that Luigi's Box is suitable for any business or industry platform on the online market.

Algolia is an API platform for dynamic experiences that helps businesses maximize the speed of search and discovery, while solving the pain of relevance tuning through AI. Accessing the right piece of content on websites and apps has never been faster or more intuitive. Algolia Search is a powerful, fully hosted API that delivers content to users in milliseconds. Developers can customize the relevance of their user experience and get insights on how users interact with it. Algolia Recommend is a robust API that allows you to build unique product recommendations into any digital e-commerce experience.

Utelly offers the best content discovery toolkit available for TV and OTT clients. To provide a comprehensive view of all content, we ingest core metadata catalogues. We also ingest individual feeds that are matched to the core metadata to create an enriching unified dataset for content discovery. Our AI enrichment modules enable sparse data sets that can be enhanced and used to improve content discovery experiences. Our search can be indexed on individual catalogs or a universal dataset, to provide an entertainment-focused search capability which is a future-proof approach to providing your customers with a great search experience. Our powerful recommendation engine uses the most recent ML/AI techniques to generate personalized suggestions based on key indicators that are identified during a user's life cycle and ingest datasets.

Personalized recommendations for entertainment platforms Rumo is a SaaS recommendation engine for entertainment content platforms. Our tool allows you to make personalized recommendations to increase user acquisition, retention, and the discoverability of content. This recommendation system is for creative content. Rumo is a flexible recommendation tool that can be used in any creative industry. Our number one priority will be to help your users find the content that they love. Get an easy overview of what recommendations can be displayed for any given piece. The similarity score is a measure of how items relate to one another. Rumo creates profiles that compile anonymous interactions from users on your platform to provide insight into their tastes and preferences. Each user is unique, so each user requires unique recommendations. Your users should stay longer on your platform. You can become the video clerk that helps customers find new topics and content.

You can orchestrate individual shopper experience at scale. Through brand inspiration and creativity, empower discovery by creating an emotional connection between consumers and brands. Respond to shoppers' needs at every moment. A micro-experience that is unique and relevant to the context of the interaction and the stage they are at in their shopping journey will be a memorable one. All engagement moments can be integrated across all devices, channels and locations to connect the shopper's journey. Optimize every stage of your shopper journey to meet your commercial goals. Your expertise can enhance algorithm-driven intelligence. Your technology stack should evolve. Keep your focus on the innovation components that make an impact. Eliminate silos with a single intelligence layer that delivers actionable insight.

Personalized suggestions--discovered through the things you already love. TasteDive allows you to discover new music, movies and TV shows, books, authors and games, as well as people who share your interests. You can also get suggestions as a visitor by using our recommendation engine. You can also stay a while, create a profile, discover interesting people and learn about cool movies, books, or games by visiting their profiles. To experiment with the API, feel free to ask for a few questions. You will need an access key to use the API. This key allows you to make 300 requests per hour. Please include a description of the product and some usage estimates. This will allow us to increase the quota for certain applications that require it, and gain a better understanding about how the service is being used. Register to save your discoveries, create inspirational lists, receive personalized recommendations, and connect with like-minded peers.

The fastest way to relevant search and recommendations. Increase engagement, conversion and revenue using a configurable, real-time system. We help your users find the content or products that are most relevant for them by surfacing those products. We do this while taking into consideration your business objectives in order to ensure that all sides of your marketplace or platform are being optimized fairly. Shaped is an automated, real-time recommendation system that consists of four stages. It contains all the data, machine-learning, and infrastructure required to understand and serve your discovery needs at scale. Connect and deploy quickly with direct integration into your existing data sources. Ingest and rerank in real-time based on behavioral signals. Optimize LLMs and neural rankings models to achieve the best performance. Build and experiment with retrieval and ranking components for any use cases.

Show your customers that you are able to understand them and earn their trust. Google has spent years creating recommendations across its flagship properties, such as YouTube, Google Search, Google Ads, and Google Search. Recommendations AI uses that machine learning expertise and experience to provide personalized recommendations that are tailored to each customer's preferences and tastes across all touchpoints. Customers will love more of the things they love. You don't need to preprocess data or train or hyper-tune machine-learning models, load balance or manually provision your infrastructure for unpredictable traffic spikes. We do it all automatically. Google's machine learning models and expertise in recommendation technology allow you to take advantage of their expertise. They can correct for seasonality and bias, and excel in situations with long-tail items and cold-start users. Integrate data, manage models and make recommendations to improve performance.

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.

roboMUA, an AI startup, is revolutionizing how people shop for beauty products. Our platform uses advanced machine-learning & artificial intelligence algorithms, an augmented reality system, and unique inclusive data sets covering over 100 skin colors to provide personalized recommendations for beauty products. This includes skincare, makeup, and fashion (shape/bodywear), all from the convenience of your smartphone. No need to visit a store. Our platform also offers a variety of educational tools and resources to help users make informed decisions about their beauty regimens, such as curated makeup tutorial videos that showcase specific makeup products from different brands. Over 50 beauty brands are currently represented in our algorithms. We offer custom algorithms via cloud APIs and Chrome Extension, Shopify Apps, Android and iOS Mobile Apps. roboMUA is developing the next-generation beauty retail using AI. roboMUA is your personal makeup artist in your pocket.

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.

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.

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.

Look no further if you are looking for a personalization solution that will increase sales, customer engagement, and provide better insight into your customers than any other solutions. Imagine a tool that knew the preferences of your customers before they visited your site and could recommend the right products to them at the right time. Segmentify provides a personalized shopping experience at every touchpoint for each customer, giving you an advantage over your competitors. Segmentify, powered by machine-learning technology tracks and targets individual website visitors based on their unique online shopping habits better than any personalisation tool on the market. Forbes named us one of the top machine-learning companies to watch.

To get people consuming, subscribing, and engaging with your content, Froomle provides AI powered recommendations that help your user access the right content regardless of the channel. Froomle is composed of experts in recommender systems for the digital publishing & eCommerce industry allowing us to offer an extensive catalog of specialized modules that are tailored to meet your specific business needs.

To make health breakthroughs more rapid, people must be involved in research. We have created a platform that connects individuals, communities, researchers, and others through trust, transparency, shared value, and shared benefit. Every person has unique information that could lead to the next medical breakthrough. Sharing your health data can help uncover new insights. Communities bring people together to quickly find answers. We manage your data and health experiences so you can start right away. We bring together individuals and communities to share their health data in order to answer the most pressing questions of life. People can unite with a common vision of fairness and responsibility, and it can change the face of established systems and institutions. A team of passionate technology and genomics leaders created it.

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.

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.

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.

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.

The Genome Solution allows enterprises from all industries to harness the power of analytics to offer highly personalized experiences to their customers. The solution allows enterprises to capture customer behavior across all channels, including digital, social, offline, and data residing within an enterprise. It then collates it based upon behavioral attributes (genomes). The solution includes over 5,000 pre-made customer genomes. This allows enterprises to optimize data preparation and analysis time, which frees up 80% of the time required to prepare the data. This significantly increases the time available for data analysis. It also provides a foundation for prescriptive and predictive analytics to enable persona-based contextual insights.

Kanteron Platform ingested digital pathology slides, medical images, and patient data from modalities and sequencers. It then provided a complete data toolkit for all hospital network teams. Precision Medicine at the point-of-care: Pharmacogenomics is used to prevent adverse medication events. It also incorporates data sources that have drug-gene interactions that were not previously available in easily accessible formats (e.g. Tables in a PDF document) and implementing the major Pharmacogenomic Databases (like PharmGKB or DGIdb, OpenTargets ...). This allows the user to refine their query to specific gene families, types, interactions, etc. Flexible AI allows you to choose the data set that is most appropriate for your use case and then apply it to your relevant medical images.

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.

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.

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.

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.

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.

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.

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.

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.

Dendi is a configurable LIS platform that gives clinical labs the flexibility to support a variety of modalities (toxicology, clinical chemistry, molecular, PGx, CGx, genomics, and more). Designed by a team of medical lab experts and modern software developers, the end product is one that hundreds of lab professionals trust for high-volume and novel testing workflows.

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.

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.

GeoMx Digital Spatial Profiler allows you to quickly resolve tissue heterogeneity, and the complexity of the microenvironment with the most flexible and robust multi-omic spatial platform for analysis of FFPE tissue sections and fresh frozen tissue. GeoMx is a spatial biology platform which non-destructively profiles RNA and proteins from distinct tissue compartments, cell populations and an automated workflow that integrates standard histology staining. You can spatially profile the entire transcriptome and over 570 protein targets, either separately or simultaneously, using your choice of sample inputs. These include whole tissue sections (WTS), tissue microarrays or organoids. GeoMx DSP is the spatial biology platform you should choose for biomarker detection and hypothesis testing. Let the tissue guide you with a biology-driven profile that allows you to select the tissue microenvironments or cell types that are most important to you.

This free tool provides stunning visualizations of genomic data, giving you the power to see exactly what is happening at each base pair within your samples. GenomeBrowse is a desktop application that runs natively on your computer. You no longer have to compromise on speed or interface quality in order to achieve a consistent experience across platforms. It was designed with performance in mind, to provide a faster browsing experience than any genome browser currently available. GenomeBrowse has also been integrated into the powerful Golden Helix VarSeq annotation and interpretation platform. VarSeq is a powerful tool for filtering, analyzing, and annotating your data. If you enjoy the visualization experience provided by GenomeBrowse then try it out. GB can show all your alignment data. You can find context-relevant findings by looking at all your samples together.

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.

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.

Illumina DRAGEN Secondary Analysis is a comprehensive and accurate analysis of next-generation sequence data. Machine learning and graph reference genome drive unprecedented accuracy. Ultra-efficient workflow. Can process a whole 34x human genome in under 30 minutes using DRAGEN server version 4. Reduces FASTQ files up to 5x, resulting in an ultra-efficient workflow. Analyzes data from next-generation sequencing (NGS), including whole genomes, transcriptomes, methylomes and exomes. Available on the platform of your choice and scalable according to needs. DRAGEN analysis is the most accurate for germline and somatic mutation calling, as demonstrated by precisionFDA's industry challenges. DRAGEN analysis allows labs of any size and discipline to do more with genomic data. DRAGEN analysis is based on highly reconfigurable FPGA technology to provide hardware-accelerated implementations for genomic analysis algorithms.

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.

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.

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.

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).

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.

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.

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.

Universal Analysis Software (UAS), a platform that analyzes and manages forensic genomic data, simplifies complex bioinformatics. The UAS is an all-inclusive solution that includes analysis modules for all ForenSeq workflows, including ForenSeq MainstAY and ForenSeq Kintelligence. It also contains ForenSeq DNA Signature prep, ForenSeq DNA Whole Genome, ForenSeq Control Region, ForenSeq mtDNA Whole Genome and ForenSeq UAS Control Region. UAS quickly generates FASTQ files and performs alignment. It also calls forensically relevant variants using NGS data. The extensive testing behind UAS's variant calls ensures that they are reliable and deliver accurate results in a user-friendly package that does not require per-seat licenses. UAS is a tool for forensic analysts. It streamlines the handling of base-bybase sequence information. It also includes a variety of features that allow you to perform everything from a quick review of everyday STR profiles to detailed analysis on the most difficult samples.

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.

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.

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.