Alternatives to G6GFINDR System

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, test PCR and sequence primers, and design and test them. CRISPR tools are powerful and make it easy to analyze your editing results, find sites, and design guide RNAs. Pre-processing NGS data with extensive tools for downstream analysis produces clean sequences. Create phylogenetic tree using peer-reviewed algorithms.

A robust platform for automatic variant prioritization and clinical interpretation, as well as report generation, is essential to ensure efficient reporting of NGS-based clinical trials. Strand Omics, a cloud-based platform that is HIPAA-compliant and fast, drives our clinical diagnostics practice. It has been refined over 4 years with over 10,000 clinical reports and multiple peer reviewed publications. Strand Omics is a combination of bioinformatics algorithms and curated databases, visualization interfaces, and reporting capabilities. It offers specialized workflows that can be used for rare inherited disorders and somatic tumor profiling tests. The platform has over 10,000 variants curated to oncogenicity, 100 genes that are curated for druggability across multiple types of cancer, and 500 drugs that have been curated for evidence.

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.

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.

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.

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).

Metabolon offers the largest Level 1 library available in the metabolomics field. Over 5,400 entries are contained in our proprietary library, which has been built over 20 years. The majority of entries are Level 1, accounting for approximately 85% of our library (4,600 entries). However, some are level 2 (approximately 15 % of the entries), due to a lack commercial standards to qualify for Level 1. Metabolon's unmatched library breadth, industry-leading annotation confidence level and unmatched library depth enable us to provide our clients with accurate, highly actionable insight for their scientific or clinical inquiries. Metabolomics is applicable to a wide variety of research, including soil health, food nutrition, preclinical research and clinical trials. Whether you are looking for trends within a group, or modifying an individual's treatment plan, metabolomics will help you find the answers you need.

Data management and simplified Bioinformatics are ideal for labs that are just getting started or for those who want to scale up their next-generation sequencing operations quickly. BaseSpace Sequence hub is an integral part of the BaseSpace Suite and is a direct extension to your Illumina instruments. BaseSpace Sequence hub allows you to manage your data with ease using a set of curated analysis apps. BaseSpace Sequence hub is powered by Amazon Web Services. Provides a secure environment. You can set up runs and monitor the quality of instrument runs. By converting sequence data into a standard format, and streaming it directly to the cloud, this tool promotes efficiency. Access to computing resources is available without the need for capital expenditures. Access to a variety of genomic analysis apps, whether provided by you, Illumina or third parties, increases organizational productivity.

Qlucore Omics Explorer makes it so simple to use that you don't have to rely on a specialist in bioinformatics for analysis and exploration of your Omics or NGS data sets. Qlucore Omics Explorer, a next-generation D.I.Y bioinformatics software, is available for research in academia, life science, and plant-tech industries. The flexible and powerful visualization-based data analysis tool delivers instant results and allows for the exploration and visualization of large data. The software was designed to allow you to choose the best workflow for your experiments and maximize the results of your research. You will be able see your results instantly by combining instant visualization with powerful statistics, flexible selection methods, and powerful statistics. You decide the workflow and starting point for your own exploration. You have complete control over the exploration process and can tailor it to your needs.

ESP is a unified, composable, and bimodal platform with a single data fabric that reduces the total cost of operations while enabling digital transformation for life sciences + healthcare. This FDA-compliant platform includes a number of best-in-class apps, including ELN, LIMS and Sample Management. ESP's REST API library and Python SDK enable flexibility and extensibility to meet customer-specific requirements. Each release is constantly updated with new applications. ESP ships with a wide range of pre-built connectors to lab Instruments, bio-process equipment, analytics, AI/ML, 3rd party software systems (such as ERP, CRM, EMR, etc.) logistics systems, bar-code printers, etc.

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.

HyperProtein, Hypercube, Inc.'s latest product, focuses on the computational science of protein sequences. The product allows you to analyze one-dimensional sequences of protein as well as subsequent three-dimensional structures. The product's most important feature is the relationship between structure and sequence. HyperProtein is not like other software programs that can perform specific functions, such as sequence alignment or protein sequence sequence, but it does combine a variety of Bioinformatics tools and Molecular Modeling tools that are related to the science that begins with a protein sequence.

Ruffus is a Python computation pipeline library. It is open-sourced and powerful, user-friendly, and widely used for science and bioinformatics. Ruffus was designed to automate scientific and other analyses with minimal fuss and effort. It is suitable for even the most basic tasks. Even complex pipelines can be handled. This will prevent make or scons from becoming cross-eyed and recursive. No "clever magic", no pre-processing. The lightweight syntax, which does one small thing well, is unambitious. Ruffus is licensed under the permissive MIT-free software license. This license allows for free use and inclusion in proprietary software. It is a good idea to run your pipeline in a temporary directory that is not connected to your original data. Ruffus is a lightweight Python module that can be used to build computational pipelines. Ruffus requires Python 2.6 and higher, or Python 3.0 and higher.

Pluto was founded in 2021 by the Wyss Institute of Harvard University. It has been a trusted partner for many life sciences organizations across the country, from biotech start-ups and public biopharma companies. Our cloud-based platform allows scientists to manage all their data, run bioinformatics analysis, and create interactive visualizations that are published-quality. The platform is being used for a variety of biological applications. These include preclinical and translational science research, cell and gene therapies and drug discovery and development.

We build products with our in-house chemists, biologists and clients to deliver outstanding performance and scientific understanding. Chemaxon offers a wide range of products, including out-of-the box solutions for scientists and IT professionals. It also includes components that add extra functionality as well as integrations with 3rd-party software, such Microsoft Excel or KNIME. Chemaxon, a leading software provider, is trusted by more than one million users. Its industry-leading tools for scientific discovery include calculation, search, and drawing tools. Our applications are used widely in education and research in the life sciences. Our clients come from a wide range of industries. The majority of major pharmaceutical companies are among them. Our offices are located at Budapest, Basel and Boston, with distributors all over the world.

Emedgene streamlines tertiary analyses for germline research and rare disease genomics. Emedgene was designed to speed up the time and certainty of user-defined variant interpretations, prioritizations, curations, and research reports. Automate your tertiary analyses with explainable AI and automation that supports genomes, exomes and virtual panels. Unify your NGS instruments and your IT systems in order to simplify and secure the entire workflow. With the latest knowledge graph options, curation abilities, and a team to support you, you can confidently keep up with evolving science, technologies, and demand. Automated workflows and explainable AI (XAI), which can be used to increase throughput without adding more staff, are a great way to do this. Implement a high-throughput WGS,WES, virtual panel or targeted panel workflow integrated into your lab's ecosystem.

Avogadro, an advanced molecule editor/visualizer, is designed for cross-platform usage in computational chemistry and molecular modeling. It provides high-quality rendering and a powerful plugin structure. Avogadro, a free and open-source molecular editor/visualization tool, is available for Mac, Windows, and Linux. It can be used in computational chemistry and molecular modeling as well as materials science and other related areas. It provides flexible, high-quality rendering and a powerful plugin structure.

Stop messing around with broken informatics tools and cloud infrastructure. Get started today on uncovering biological insights. Scientists are often limited by the fragmentation of tools across biology and bioinformatics teams. To help teams accelerate their R&D, we created a harmonized platform for bioinformatics between the cloud and the wet lab. Import raw data from your cloud service provider, your team's instruments, or your cloud. Create and deploy custom bioinformatics workflows using any language. Stop wasting time tinkering with your infrastructure. You can easily run any workflow and keep track of every analysis. Interactive visualizations of NGS data ready-to-go with point-and click plots Latch integrates with your AWS S3. You can access hundreds of terabytes in organic filesystems you are familiar with. Create bioinformatics workflows, and dynamically create no-code interfaces with Python with tunable storage and compute.

Swiss-PdbViewer, also known as DeepView, is an application that allows you to analyze multiple proteins simultaneously. To compare active sites and other parts, the proteins can be superimposed. The intuitive interface and graphic make it easy to find information about amino acid mutations, Hbonds, angles and distances between atoms. Nicolas Guex has been developing Swiss-PdbViewer (aka DeepView), since 1994. Swiss-PdbViewer was originally tightly connected to SWISS-MODEL (an automated homology modeling server) that was developed at the Structural Bioinformatics Group of the Biozentrum in Basel. The SWISS-MODEL interface has evolved to the point that advanced modeling can now be done directly. It is no longer possible to maintain a direct interface with SwissPdbViewer.

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.

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.

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.

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.

IDBS Polar is the first BioPharma lifecycle management (BPLM) platform in the world. It eliminates repetitive manual tasks and allows you to execute your processes efficiently while curating data. This will allow you to accelerate the time to market, by tackling the most challenging challenges of process design, optimization scale-up and technology transfer. Interactive data analytics applications such as bioreactor comparision designed specifically for biopharmaceutical development scientists. IDBS Polar is an integrated platform that manages drug progress in contexts such as workflow, integration and insight. Workflows designed for the BioPharma lifecycle, with process-aware design, planning, and execution. Integrations that give meaning to your data. Rapid integration into your development environment, enabling automation, and curating a data backbone based on processes.

Legacy R&D software can be a drain on scientific potential. It slows down R&D progress and scatters data between silos. Benchling is the industry's most trusted life sciences R&D cloud. All the tools you need to accelerate, measure, and forecast R&D, from discovery through bioprocessing, all in one place. A suite of seven applications that are natively unified and can be used to accelerate R&D at all levels. Open integration, codeless configuration, and dashboards that are tailored to your needs. For continued success, deep life science R&D and consulting expertise are essential. Benchling is a unified R&D platform that allows you to spend less time searching for data and more time working together in order to advance your research. Scientists, managers, executives, and researchers can optimize R&D output by having complete visibility into the experimental context, program performance, resource utilization, and program performance.

The XetaBase platform is unique in that it simplifies tertiary analyses by aggregating, indexing and enriching secondary genome data. This allows for a continual reinterpretation of the data to unlock clinical and research insights. XetaBase enables the rapid management of genomic data and its cost-effective use in the laboratory and clinic. XetaBase is a genomic-scale platform. The greater the volume and the complexity, the better the insights and outcomes. XetaBase, a genomic-native platform, is built on the OpenCB open-source software platform. It meets the demands of genomic medicine for speed, scale, and reinterpretation. Zetta Genomics provides genomic data management that is fit for the precision-medicine age. XetaBase offers a novel solution for the challenges of genomic information. It replaces outdated flat file approaches and brings meaningful and actionable genome data to the lab and clinic. XetaBase allows for continual reinterpretation and scales seamlessly as databases expand to include genome sequences.

Microsoft's experience and scale in managing exabyte-scale workloads can be used to reduce the need for you to manage your own data center. Microsoft Genomics on Azure gives you the performance and scalability that comes with a supercomputing facility of the highest caliber, all on demand. Take advantage of an MPI backend network that has a latency of under three microseconds, and a non-blocking throughput of 32 gigabits per seconds (Gbps). This backend network features remote direct memory access, which allows parallel applications to scale up to thousands of cores. Azure offers high memory and HPC class CPUs to help get results quickly. Scale up or down according to your needs and only pay for what you actually use. Azure's worldwide network of data centers can help you meet your compliance needs and address data sovereignty issues. Easy integration into your existing pipeline code with a REST API and simple Python client.

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.

Polly allows you to harness the power of biomedical information. The Polly Platform allows you to scale batch jobs, workflows and visualization applications. Polly supports resource pooling, optimizes resource allocation based upon your usage requirements, and makes use of spot instances when possible. This results in optimization, efficiency, quicker response time, and lower costs for resources. Access a dashboard that allows you to monitor and track resource usage and costs in real-time. This will allow you to reduce overheads when resource management is done by your IT team. Polly's infrastructure is built around version control. Polly uses a combination dockers and interactive notebooks to ensure version control for your analyses and workflows. We have created a mechanism that allows data, code, and the environment to co-exist. This, along with cloud data storage and the ability for users to share projects, ensures reproducibility in every analysis.

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.

How can you make a profit from a 20% fee account? These are the most difficult problems we face with existing technologies. Artificial intelligence and expert systems are the best options. "Expert systems" are computer programs which can imitate the behavior of a human expert. Artificial intelligence is a term used to distinguish it from "human intelligence". This term is associated with memory lapses, inconsistencies and fatigue, as well as the need for vacations. Quantrax Corporation in 1990 proposed, designed, and built a new software system that would use artificial intelligence as its foundation, changing the software landscape forever. Understanding the product and the development process is key. One must understand the differences between expert systems and traditional data-based systems. Data-based systems are computer programs that use data to produce results.

ResoluteAI's secure platform allows you to search multiple databases, including scientific, regulatory and business databases. Combining interactive analytics with downloadable visualizations, you will be able to make connections that lead directly to breakthrough discoveries. ResoluteAI's enterprise product for science is Nebula. Your institutional knowledge is enhanced by structured metadata and a variety of AI capabilities. This includes NLP and OCR, image recognition, transcription, and other AI capabilities that make your proprietary information easily searchable and accessible. Nebula gives you the ability to unlock hidden value in your research and experiments, market intelligence, acquired assets, and other research. Structured metadata is created from unstructured text. This includes semantic expansion, conceptual searching, and document similarity searches.

JobArch is an easy-to-use and powerful Applicant Ranking System. It allows for efficient and affordable recruitment and selection. It is a modern version of a traditional ATS that uses Artificial Intelligence to read CVs and job requirements and then automatically match them by ranking applicants with searches. The system does all the pre-screening. JobArch uses Artificial Intelligence to analyze all incoming CVs, match offers, and create applications. Our integrated technology for skill match allows us to identify the best candidates and to recognize those who are most compatible with the job openings. Main features: - AI CV Matching cross-language - Ranking of candidates sorted by % of compatibility of hard and soft skills - JobArch Candidate Database always consultable - Match, not only actives candidates, but of all candidates in the DB - Integrated multiposting - Employer branding - Customized question and and psycho-aptitude test to assess candidates - Available in 6 languages - CRM

Skillskan by Arca24 brings the best AI recruiting technology available as a web service for staffing and corporate organizations to empower their talent acquisition strategy. Our Artificial Intelligence multilingual tools include: - Resume and job matching: match resumes to the job offer and quickly draw up a shortlist of candidates or employees to fill a vacancy, ranked from most to least compatible. - Semantic search: discover the true value of your candidate database, leverage the applications you already have to complete a job search faster. - Resume parser for text and images: turning the millions of applications into structured data to create a structured database of candidates for a digitized recruitment process. - External sourcing: boost your talent acquisition by hunting candidates in multiple databases - Lead generator: discover the labor market to support your strategic plan and use our semantic search system to analyze data - Tools to develop an advanced search system in your ATS: create an advanced search system in your ATS: extract a content from different sources, normalize a text and identify semantic tags to create semantic searches.

Data engineers and scientists can be 95% better at their jobs with ready access to the most flexible semantic layer, explainable AI and reusable data modelling. They can create and expand semantic models, understand data interrelationships, and run federated query to speed up time to insight. Stardog's graph data virtualization and high performance graph database are the best available -- at a price that is up to 57x less than competitors -- to connect any data source, warehouse, or enterprise data lakehouse without copying or moving data. Scale users and use cases at a lower infrastructure cost. Stardog's intelligent inference engine applies expert knowledge dynamically at query times to uncover hidden patterns and unexpected insights in relationships that lead to better data-informed business decisions and outcomes.

Haystack’s pipeline architecture allows you to apply the latest NLP technologies to your data. Implement production-ready semantic searching, question answering and document ranking. Evaluate components and fine tune models. Haystack's pipelines allow you to ask questions in natural language, and find answers in your documents with the latest QA models. Perform semantic search to retrieve documents ranked according to meaning and not just keywords. Use and compare the most recent transformer-based language models, such as OpenAI's GPT-3 and BERT, RoBERTa and DPR. Build applications for semantic search and question answering that can scale up to millions of documents. Building blocks for the complete product development cycle, including file converters, indexing, models, labeling, domain adaptation modules and REST API.

Security is a key part of our business. That's why Active Directory settings are the most secure distribution of rights. This ensures that files are only visible to the person who has been assigned. Many companies desire their own innovative search for the website and intranet. The Hulbee Enterprise Search software allows you to perform a semantic search that returns relevant results. You can also customize your search with API and SDK. Many companies are very technical and can adapt Hulbee Enterprise Search to suit their needs. We would be delighted to offer this opportunity! You can modify and expand our software in the same way as a Lego system. Everything can be linked via API and expanded with SDK, no matter if it is intranet or internet. You can also connect to our search your own development environment, so you are not dependent on third parties.

In a single environment, you can manage all activities of collegiate bodies within your organization. In less than three minutes, you can prepare and call complete meetings. Integrating agendas, materials, and participants' calendars with attendance management. Atlas Bluebook consolidates all meeting data into one file with single pagination. Bluebook converts all documents into a single pdf file and watermarks every page to ensure information security and traceability. You can make appointments, take notes and share them with others. Bluebook will save any annotated material that is deleted or overwritten. Your minutes are automatically based on information such as organization, collegiate, date and time, place, participants, agendas and deliberations. You can search within the system and files for words, documents, and terms. This is done using artificial intelligence to optimize your search.

Adsby can increase the effectiveness of your Google Search campaigns by up to 5x. We understand the challenges faced by business owners. Due to limited budgets and fierce competition, each ad click counts. We've created a tool that optimizes your ad's performance and reach. Immerse yourself in a world where advertising and artificial intelligence meet. Adsby AI analyses, adapts and amplifies your campaigns, ensuring they are always one step ahead. No more waiting, no more second-guessing. Our AI quickly generates eye-catching ad text, ensuring that your message is memorable and resonates. Our high-performance keywords will help you reach more people. Our negative keyword insights will help you avoid pitfalls and make sure your ads are seen by the right people. Adsby's daily AI-optimizations ensure that your campaigns are optimized to maximize growth and return. Adsby helps you create Google search ads easily with the help of artificial intelligence.

Revseed is a Strategy Management System that helps in hotel revenue management and data analytics. It is a leading company that offers hotel revenue management strategies that focus on volume, rate and market-linked availability with Artificial intelligence (AI) & Machine learning(ML) and Algorithms.

Artificial intelligence can help you improve your Google presence. "Hack The SEO", a SEO booster, boosts your SEO through an analysis of your traffic and positions. It performs a thorough search for relevant keywords and automatically creates articles. With just a few mouse clicks, you can see a rapid rise in your traffic. Write SEO articles in five minutes with AI that generates traffic Hack the SEO gives you all the keys for a site to soar on Google. Keyword research - Writing with real time data on the topic - Analysis of competitors SEO optimization NLP editor Hack the SEO's NLP semantic analysis (Natural Language Processing), which optimizes SEO, involves understanding and interpreting content. It analyzes the relevance and importance of words and phrases with respect to specific topics in order to enhance the content's visibility on search engines.

The Keyword Explorer allows you to fine-tune your keyword strategy. It takes the guesswork out keyword selections and targets audiences with precision. Our intuitive system gives you insight into the business of your competitors without wasting any time or energy. You can spend your time on brands and wholesale products that are in high demand, earning great profit. No more frustration and uninformed product choices. Our data-rich tools will help you improve efficiency and make your arbitrage business more lucrative. Compare how your products and those of your competitors rank against a keyword. Search our database of more than 10M products to assess the competition level. Advanced Search can be used to find out more about your niche.

Semantee, a managed database that is easy to configure and optimized for semantic searches, is hassle-free. It is available as a set REST APIs that can be easily integrated into any application in minutes. It offers multilingual semantic searching for applications of any size, both on-premise and in the cloud. The product is significantly cheaper and more transparent than most providers, and is optimized for large-scale applications. Semantee also offers an abstraction layer over an e-shop's product catalog, enabling the store to utilize semantic search instantly without having to re-configure its database.

Use user feedback and semantic relevance to reliably retrieve optimal document chunks for your retrieval-augmented generation system. In your search system, combine semantic relevance with document freshness because recent results are more accurate. Create a personalized ecommerce feed in real-time using user vectors based on the SKU embeddings that were viewed by the user. A vector index in your warehouse can be used to discover behavioral clusters among your customers. Use spaces to build your indices, and run queries all within a Python Notebook.

Our executive management system creates value in a data-driven manner. All you need in one executive administration system. Our artificial intelligence and industry benchmarks combine to optimize your recommendations. Streamline your planning based on your data. Fully integrated and intelligent executive management suite. One system for planning and reporting. Deep industry-specific content and best practices. Relevant semantic data model, KPIs/dashboards, deep-drills, benchmarks, recommendations, etc. The standard solution is easier, cheaper, and quicker to set up. For quick setup and operations, no IT or BI team are required. Executives will find it easy to use Excel for a flexible and simple user experience. P&L prediction, root cause analysis, and recommendations are all part of the intelligent integration technology-powered industry-specific data schema.

IntraFind's Enterprise Search Solution iFinder is a central platform for all your company's data. iFinder can be connected with all data sources in your company. Are your data sources constantly growing? iFinder will help you be ready for the future. Our product is based upon Elasticsearch technology, and can adapt to any amount of data with ease. It improves search results by using artificial intelligence to deliver intelligent enterprise search functionality. iFinder allows you to find important data and documents on company drives, intranets, wikis, e-mail systems, or on company drives. Our enterprise search application will allow you to centralize access to all company data, enabling you to take the next step in your company’s digital transformation. iFinder enhances search results by deploying AI to deliver smart enterprise search functionality.

Anolytics offers data annotation services for image, video and text for machine learning and AI based computer vision. Anolytics provides low-cost annotation services for machine learning and the development of artificial intelligence models. It provides the annotated data in text, images, and videos using various annotation techniques. It also ensures the quality and accuracy. It is highly skilled in Image Annotation, Video Annotation, and Text Annotation. Anolytics provides all the leading data annotation services used for data training in machine learning or deep learning. It provides Bounding boxes, Semantic Segmentation and 3D Point Cloud Annotation as well as 3D Cuboid Annotation. These services are useful in fields such as healthcare, autonomous driving, drone falying, security surveillance, agriculture, and retail. Anolytics offers a scalable solution that is available quickly and at a cost-effective price for clients around the world.

Clarity's technology uses multiple layers of artificial Intelligence and automation to comb through global networks in search of an unprecedented quantity of data. Our team of analysts uses their expertise to create a report which gives you the best from both worlds. We process and deliver results faster than anyone else in the industry, whether you order a comprehensive report or an automated one. Intelligo's expanded data sources can uncover potential red flags that manual searches may miss. AI allows for extensive searches across multiple data sources, covering much more information than could be achieved with a traditional background search. Analysts with years of experience collect manual data, review results that are automatically matched, and confirm automated flags to ensure transparency. Interact with your team by adding comments and tagging colleagues. Share reports, or integrate your due diligence system.

AI-powered ATS and CRM can revolutionize recruitment productivity and accelerate hiring. Our applicant tracking system allows you to distribute jobs, search for applicants across major job boards, and use intelligent semantic search in order to find and rank the most qualified candidates based on their experience. You can also bulk upload resumes and smart parse them for future searches. Send marketing campaigns to different audiences and move candidates through the interview pipeline faster. Boost hiring and recruiting productivity metrics by planning and assigning projects, collaborating with internal and external teams and tracking and analyzing the project statuses using Kanban boards.

OpenAI's mission, which is to ensure artificial general intelligence (AGI), benefits all people. This refers to highly autonomous systems that outperform humans in most economically valuable work. While we will try to build safe and useful AGI, we will also consider our mission accomplished if others are able to do the same. Our API can be used to perform any language task, including summarization, sentiment analysis and content generation. You can specify your task in English or use a few examples. Our constantly improving AI technology is available to you with a simple integration. These sample completions will show you how to integrate with the API.