Alternatives to GeneXproTools

Compare GeneXproTools alternatives for your business or organization using the curated list below. SourceForge ranks the best alternatives to GeneXproTools in 2026. Compare features, ratings, user reviews, pricing, and more from GeneXproTools competitors and alternatives in order to make an informed decision for your business.

  • 1
    CZ CELLxGENE Discover
    Select two custom cell groups based on metadata to find their top differentially expressed genes. Leverage millions of cells from the integrated CZ CELLxGENE corpus for powerful analysis. Execute interactive analyses on a dataset to explore how patterns of gene expression are determined by spatial, environmental, and genetic factors using an interactive speed no-code UI. Understand published datasets or use them as a launchpad to identify new cell sub-types and states. Census provides access to any custom slice of standardized cell data available on CZ CELLxGENE Discover in R and Python. Explore an interactive encyclopedia of 700+ cell types that provides detailed definitions, marker genes, lineage, and relevant datasets in one place. Browse and download hundreds of standardized data collections and 1,000+ datasets characterizing the functionality of healthy mouse and human tissues.
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    GeneXus

    GeneXus

    Globant

    Simplify and Automate Software Development with GeneXus GeneXus is a Low-Code Platform powered by AI that simplifies and automates software creation. By modeling instead of coding, it generates complete solutions—from user interfaces to backends—faster and with less complexity. With 35+ years of experience, GeneXus helps enterprises build scalable, AI-driven systems, modernize legacy software, and adapt to new technologies without rework. It supports development across web, mobile, and desktop platforms, seamlessly integrating databases, APIs, and enterprise systems. Trusted in over 50 countries, GeneXus is a leader in the low-code market.
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    SnapGene

    SnapGene

    SnapGene

    Accurately design and simulate cloning procedures. Test complicated projects, catch errors before they happen, and obtain the right constructs the first time. Cloning is easier when you can see what you are doing. The intuitive interface offers you unparalleled visibility into your work, simplifying often complex tasks. SnapGene automates documentation, so you don’t have to. See and share every sequence edit and cloning procedure that led to your final plasmid. Improve your core molecular biology procedures, and improve your results. Master SnapGene and key concepts in cloning with our new online learning center, SnapGene Academy. Containing over 50 video tutorials taught by scientific experts, SnapGene Academy helps you advance your skills across multiple molecular biology courses. SnapGene 7.2 provides a new visualization of primer homodimer structures and enhancements to file management, allowing tabs to be organized in multiple windows using drag and drop.
    Starting Price: $295 per year
  • 4
    ProcessGene BPM Software
    ProcessGene is the leading provider of software solutions for Business Process Management (BPM). The BPM software solutions are implemented within days, immediately creating visibility and centralized control. Businesses and governments worldwide use the ProcessGene™ BPM software cloud to manage, control and improve business processes, implement enterprise software, and coordinate mergers and acquisitions. ProcessGene™‘s BPM software is designed for multi-subsidiary organizations, based on our Multi-Org technology. ProcessGene™ has been a pioneer and global leader in Multi-Org BPM technology. During the past decade we have mastered a unique expertise in providing software solutions to multi-subsidiary organizations worldwide. Our BPM software cloud has been specifically designed for multi-subsidiary organizations and it features the most comprehensive solution for complex, distributed business process planning, improvement, and implementation challenges.
    Starting Price: $30.00/month/user
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    ProcessGene GRC Software
    ProcessGene is the leading provider of software solutions for Governance, Risk, and Compliance (GRC). The GRC software solutions are implemented within days, immediately creating visibility and centralized control. ProcessGene™ GRC software solutions establish an automated workflow that reduces the time and cost of GRC efforts and eliminate manual labor, maintenance of multiple excel spreadsheets, etc. ProcessGene™‘s GRC software solution is designed for multi-subsidiary organizations, based on our Multi-Org technology. ProcessGene™ has been a pioneer and global leader in Multi-Org technology. During the past decade we have mastered a unique expertise in providing software solutions to multi-subsidiary organizations worldwide. Our GRC software has been specifically designed for multi-subsidiary organizations and it features the most comprehensive solution for complex, distributed risk management and regulatory compliance challenges.
    Starting Price: $30.00/month/user
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    GritGene

    GritGene

    GritWorld

    GritGene is a new digital engine that is developed by GritWorld. With a fully customizable rendering pipeline and easy workflows for the user. GritGene enables filmmakers to easily produce VFX and animation in CGI quality without worrying about learning complicated game-engine pipelines. After years of hard work and internal use, GritGene is finally ready for closed beta to selected users. The current pace of the industry triggered us to push the boundaries of real-time graphics. Our integration of Raytracing is a perfect example of that. We are proud to contribute to shaping the future of real-time technology. Building the right thing at the right time and in the right way is not easy. That is exactly why we built the engine the way we did. Technology is ever-changing and therefore we want to be able to exchange solutions at any time. GritGene consists of a fully scalable rendering pipeline, with a strong innovative state-of-the-art UI framework and a scalable render core.
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    QIAGEN Ingenuity Pathway Analysis
    IPA can also be used for analysis of small-scale experiments that generate gene and chemical lists. IPA allows searches for targeted information on genes, proteins, chemicals, and drugs, and building of interactive models of experimental systems. Data analysis and search capabilities help in understanding the significance of data, specific targets, or candidate biomarkers in the context of larger biological or chemical systems. The software is backed by the Ingenuity Knowledge Base of highly structured, detail-rich biological and chemical findings. Learn more about QIAGEN Ingenuity Pathway Analysis (IPA). Comparison Analysis determines the most significant pathways, upstream regulators, diseases, biological functions, and more, across time points, dose, or other conditions.
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    E-GENE ITSM
    E-GENE ITSM is a cloud-based no-code/low-code IT service management solution developed by STEG. Built on ITIL best practices, it streamlines core ITSM processes such as incident, request, change, and configuration management within a single integrated platform. With flexible customization tools and powerful automation, E-GENE ITSM helps organizations enhance operational efficiency while maintaining compliance. Key Features • No-code/Low-code platform: Easily configure workflows, forms, and user interfaces without coding. • ITIL-compliant modules: Includes service request, incident, change, and configuration management. • Customizable UI tools: Use built-in Form Designer, List Manager, and dashboard tools to tailor the experience. • Workflow automation: Streamline complex processes and reduce manual tasks.
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    Kanteron

    Kanteron

    Kanteron Systems

    Kanteron Platform ingested medical images, digital pathology slides, genomics sequences, and patient data from modalities, scanners, sequencers and databases, and provided a complete data toolkit to every team in hospital networks. Pharmacogenomics for adverse medication event prevention, and Precision Medicine application at the point of care: Incorporates sources of drug-gene interaction data that were previously only available in in accessible formats (e.g. tables in a PDF document), implementing the major Pharmacogenomic databases (like PharmGKB, CGI, DGIdb, OpenTargets...) Allows the user to refine their query to certain gene families, types of interactions, classes of drugs, etc. Flexible AI means you can choose the data set that best fits your use case, and apply it to your relevant medical images.
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    SelfDecode

    SelfDecode

    SelfDecode

    Upload your clients’ health data to instantly generate risk scores, analysis summaries & personalized supplements, diet and lifestyle recommendations. Get better results by offering clients scientifically accurate and personalized recommendations based on their DNA, labs and environmental data. See more clients and improve retention with an easy-to-use platform that allows you to streamline your health services. See which genes are playing a role in your clients’ health issues. Build a plan to address the problem genes using the AI-generated list of prioritized recommendations. SelfDecode Labs is a simple tool giving more insight into your clients’ lab results. Order lab tests or upload results to see where levels fall related to the functional range, get suggestions to improve them & track them over time. Add recommendations to your clients’ easy-to-follow regimen. Track progress and make changes based on what’s working.
    Starting Price: $199 per month
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    Signals Translational
    With visual analytics powered by TIBCO Spotfire®, PerkinElmer Signals Translational provides all the necessary tools to harmonize, manage, search, aggregate and analyze data consistently across large datasets for use in translational research in a highly scalable manner. Powered by the industry-leading visual analytics platform TIBCO Spotfire®, Signals Translational enables precision medicine studies with the most advanced biomarker discovery and patient stratification solution available today. The Linear Mixed Effect App (LME) in Signals Translational allows scientists to rank the effect of multiple variables on a phenotype of interest, with the option to correct the effect of random variables in the analysis. The genes with the strongest impact on cancer stage progression can be identified independently of the origin of the patients. With the advantage of properly handling missing values and outliers, LME models are an effective tool to identify potential biomarkers.
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    VarSeq

    VarSeq

    Golden Helix

    Simple, fast, and repeatable variant analysis software for gene panels, exomes, and whole genomes. VarSeq is an intuitive, integrated software solution for tertiary analysis. With VarSeq you can automate your workflows and analyze variants for gene panels, exomes, and whole genomes. Understanding genomic data has never been easier thanks to our software. VarSeq software provides a powerful filtering and annotation engine to sift through large variant data sets. Using a chain of filters, you can quickly narrow your list of variants down to those that are most likely to be of interest. After determining the parameters that work well for your analysis, you can save the state of your filters so that you can easily apply the same analysis to another dataset. The same automated workflow can be used for each batch of samples, making VarSeq an ideal solution for high-throughput environments. Real-time filtering gives you the power to quickly prototype and tune analysis workflows.
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    Axie Infinity

    Axie Infinity

    Axie Infinity

    Axie is a new type of game, partially owned and operated by its players. Build unstoppable teams of Axies and conquer your enemies! Each Axie has unique strengths and weaknesses based on its genes. With billions of possible genetic combinations, the possibilities are truly infinite! Become a land baron and start your own Kingdom! Use land to farm rare resources, tokens, and attack dungeons!
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    LEADBACKER

    LEADBACKER

    LEADBACKER

    Unleash your Leadership DNA! … and become the best version of yourself! Lead effectively Inspire talents Learn playfully LEADBACKER is the standard for instant feedback in organisations focussing on a development- and learning culture. LEADBACKER is a treasure that becomes more valuable with every application – with every failure and every getting back up again, as well as with every award and praise that is given via LEADBACKER. LEADBACKER is a trusted, digital advisor that helps you realize how to develop your leadership genes and become the best version of yourself
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    Statistix

    Statistix

    Analytical Software

    lf you have data to analyze—but you're a researcher, not a statistician—Statistix is designed for you. You'll be up and running in minutes—without programming or using the manual! This easy to learn and simple to use software saves you valuable time and money. Statistix combines all the basic and advanced statistics and powerful data manipulation tools you need in a single, inexpensive package. Statistix offers powerful data manipulation tools, import/export support for Excel and text files, linear models (including linear regression, logistic regression, Poisson regression, and ANOVA), nonlinear regression, nonparametric tests, time series, association tests, survival analysis, quality control, power analysis, and more.
    Starting Price: $395 one-time payment
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    Dotmatics

    Dotmatics

    Dotmatics

    Dotmatics is the global leader in R&D scientific software that connects science, data, and decision-making. Combining a workflow and data platform with best-of-breed applications, we offer the first true end-to-end solutions for biology, chemistry, formulations, data management, flow cytometry, and more. Trusted by more than 2 million researchers from the world’s leading biopharma, chemicals and materials enterprises, and academic institutions, we are dedicated to working with the scientific community to help make the world a healthier, cleaner and safer place to live. Learn more about our platform and products, including GraphPad Prism, Geneious, SnapGene, Protein Metrics, LabArchives, and more.
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    Pluto

    Pluto

    Pluto Biosciences

    Since its founding in 2021 from the Wyss Institute at Harvard University, Pluto has become a trusted partner of life sciences organizations around the country ranging from biotech start-ups to public biopharma companies. Our cloud-based platform gives scientists the ability to manage all of their data, run bioinformatics analyses, and create interactive and publication-quality visualizations. The platform is currently being used for a wide variety of biological applications, from preclinical / translational science research, to cell and gene therapies, drug discovery and development, to clinical research.
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    Predictive Suite

    Predictive Suite

    Predictive Dynamix

    Automated variable selection identifies key variables & variable interactions. Insightful visualization of data and model dynamics. Execution of batch commands. SQL queries and dataset browsing. Pre & post-processing for creating variables, constraining outputs, etc. Models easily deployed via ActiveX (i.e., OCX) controls or DLLs. Powerful modeling algorithms include regression, neural networks, self-organizing maps, dynamic clustering, decision trees, fuzzy logic, genetic algorithms. Predictive Dynamix provides computational intelligence software for forecasting, predictive modeling, pattern recognition, classification, and optimization applications, across all industries. Modern neural network technology are powerful computational structure for solving difficult problems involving forecasting and pattern recognition. Multi-layer perceptron neural networks have an architecture that allows multiple coefficients per input variable.
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    Platforma

    Platforma

    MiLaboratories

    Platforma is a no-code bioinformatics software that converts raw next-generation sequencing (NGS) data into insights. It offers a user-friendly interface with modular, no-code "blocks" for complex analysis tasks like immune repertoire, single-cell, and gene expression data. Building on the legacy of its predecessor, MiXCR, Platforma also enables AI-powered selection for antibody/TCR candidates. The platform is designed to be accessible to scientists without a bioinformatics background, allowing for scientists to take control of their own discoveries and reduce time to insight.
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    AmpleLogic Quality Management
    AmpleLogic's Quality Management Software (eQMS) is intricately crafted to meet the rigorous requirements of heavily regulated industries. The ISO 9001 certified cloud-based Quality Management System (QMS) is ideal for Lifesciences, Food & Beverages (F&B), Cosmetics, Medical Devices, Gene Therapy, and analogous sectors. As businesses acknowledge the challenges associated with manual quality checks—prone to both laborious efforts and errors—they are increasingly adopting QMS software solutions. These systems play a pivotal role in enhancing audit quality through process automation, efficient data management, and seamless API integration.
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    Color

    Color

    Color

    Color offers one of the most accessible, clinical-grade genetic testing services available today, analyzing genes associated with risk for common cancers and heart conditions — and how the body may process certain medications. We provide a suite of services, tools, and expertise to help you enroll new patients and activate them into care journeys relevant to them over time. We use a more complete view of patient health, incorporating an individual’s genetics, personal & family health history, and lifestyle & behavior information to surface and recommend specific care or point solutions that patients can take advantage of based on their personal risks.
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    mgi

    mgi

    MARSEILLE GYPTIS INTERNATIONAL

    Visibility and predictability to optimise goods transit times. Create smooth information flows by connecting up all players in the supply chain to a door-to-door tracking goods. An optimised port information system with certified data security. At MGI, innovation is in our genes. It is a key factor for creating a smoother supply chain thanks to continuous tracability, improved predictability and faster data exchange. Big Data, blockchain, cybersecurity and Artificial Intelligence are at the heart of our innovations to provide you with a Cargo Intelligent System and prevent port congestion.
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    Bokeh

    Bokeh

    Bokeh

    Bokeh makes it simple to create common plots, but also can handle custom or specialized use-cases. Plots, dashboards, and apps can be published in web pages or Jupyter notebooks. Python has an incredible ecosystem of powerful analytics tools: NumPy, Scipy, Pandas, Dask, Scikit-Learn, OpenCV, and more. With a wide array of widgets, plot tools, and UI events that can trigger real Python callbacks, the Bokeh server is the bridge that lets you connect these tools to rich, interactive visualizations in the browser. Microscopium is a project maintained by researchers at Monash University. It allows researchers to discover new gene or drug functions by exploring large image datasets with Bokeh’s interactive tools. Panel is a tool for polished data presentation that utilizes the Bokeh server. It is created and supported by Anaconda. Panel makes it simple to create custom interactive web apps and dashboards by connecting user-defined widgets to plots, images, tables, or text.
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    KuGou

    KuGou

    KuGou

    Kugou is a digital music interactive service provider with highly technologically innovative genes in China and a leader in Internet technology innovation. It is committed to providing complete solutions for Internet users and the development of the digital music industry. In the field of technology promotion, the company has created a number of advanced innovative technologies, shared interactive networks, data transmission solutions, efficient distributed non-centralized search, song recognition technology, precise dynamic karaoke lyrics function and music recommendation management system, etc. It fills the domestic technological gap and leads the development of a new generation of Internet architecture technology.
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    NXG Logic Explorer
    NXG Logic Explorer is a Windows-based machine learning package designed for data analytics, predictive analytics, unsupervised class discovery, supervised class prediction, and simulation. It enhances productivity by reducing the time required for various procedures, enabling users to identify novel patterns in exploratory datasets and perform hypothesis testing, simulations, and text mining to extract meaningful insights. Key features include automatic de-stringing of messy Excel input files, parallel feature analysis for generating summary statistics, Shapiro-Wilk tests, histograms, and count frequencies for multiple continuous and categorical variables. It allows simultaneous execution of ANOVA, Welch ANOVA, chi-squared, and Bartlett's tests on multiple variables, and automatically generates multivariable linear, logistic, and Cox proportional hazards regression models based on a default p-value criterion for filtering from univariate models.
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    Huawei Cloud
    HUAWEI CLOUD is a leading cloud service provider, which brings Huawei's 30-plus years of expertise together in ICT infrastructure products and solutions. We are committed to providing reliable, secure, and cost-effective cloud services to empower applications, harness the power of data, and help organizations of all sizes grow in today's intelligent world. HUAWEI CLOUD is also committed to bringing affordable, effective, and reliable cloud and AI services through technological innovation. By the end of 2019, HUAWEI CLOUD had launched 210+ cloud services and 210+ solutions. News agencies, social media platforms, law enforcement, automobile manufacturers, gene sequencing organizations, financial institutions, and a long list of other industry customers are all benefiting in significant ways from HUAWEI CLOUD. 3500 applications were added to the HUAWEI CLOUD marketplace with offerings from more than 13000 business partners.
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    pidas

    pidas

    pidas

    NEXT - that is the integrated overall solution for today's IT support: For fast and convenient support . For more freedom for your internal IT specialists. And for really happy end users. Based on our many years of expertise, we have developed an integrated overall solution that enables modern and comprehensive IT support. Digital end-to-end process with a high degree of automation. End-to-end processes with integration of chatbots and IT machines. We have them! The right people for the demanding everyday support: with broad technical know-how, high commitment and the pidas service gene. This is how we always put together the right crew for you – whether in the service desk or in field support.
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    Ontosight.ai
    Ontosight is a cutting-edge research and AI-powered Q&A platform designed to revolutionize how you access and process information. Leveraging advanced artificial intelligence, Ontosight combines the precision of academic and specialized databases with the ease of conversational search. Whether you're an undergraduate, a Ph.D. student, or a seasoned researcher, Ontosight transforms traditional research into an efficient, insightful, and engaging experience. Why Choose Ontosight? Precision and Depth: Unlike generic search engines, Ontosight AI delivers highly targeted results from specialized databases, academic journals, and clinical trials. Transparency: Always know where your information comes from, with clear citations and references. Efficiency: Save hours by summarizing lengthy papers and highlighting critical insights. Exploration of Connections: Highlights relationships between entities—like genes, molecules, or treatments—helping you uncover patterns and ideas for i
    Starting Price: $11 per month
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    Evo 2

    Evo 2

    Arc Institute

    Evo 2 is a genomic foundation model capable of generalist prediction and design tasks across DNA, RNA, and proteins. It utilizes a frontier deep learning architecture to model biological sequences at single-nucleotide resolution, achieving near-linear scaling of compute and memory relative to context length. Trained with 40 billion parameters and a 1 megabase context length, Evo 2 processes over 9 trillion nucleotides from diverse eukaryotic and prokaryotic genomes. This extensive training enables Evo 2 to perform zero-shot function prediction across multiple biological modalities, including DNA, RNA, and proteins, and to generate novel sequences with plausible genomic architecture. The model's capabilities have been demonstrated in tasks such as designing functional CRISPR systems and predicting disease-causing mutations in human genes. Evo 2 is publicly accessible via Arc's GitHub repository and is integrated into the NVIDIA BioNeMo framework.
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    BigOmics Analytics

    BigOmics Analytics

    BigOmics Analytics

    BigOmics Analytics is a biodata analytics startup developing platforms for biologists to easily visualize and understand their omics data. Our flagship product, Omics Playground, is a user-friendly bioinformatics software for RNA-seq and proteomics data that allows users to store and interactively visualize data from experiments. BigOmics Analytics offers over 18 interactive analysis modules and 150+ interactive plots, enabling co-analysis with more than 6,000 public datasets and access to 50,000+ public gene sets and pathways. The platform also integrates drug connectivity and drug sensitivity databases with over 30,000 drug expression profiles. Designed to facilitate collaboration between biologists and bioinformaticians, BigOmics Analytics helps users discover more while spending less time on data analysis, all without requiring coding skills. The platform ensures robust and reproducible results by utilizing best-in-class methods.
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    Galaxy

    Galaxy

    Galaxy

    Galaxy is an open source, web-based platform for data-intensive biomedical research. If you are new to Galaxy start here or consult our help resources. You can install your own Galaxy by following the tutorial and choosing from thousands of tools from the tool shed. This instance of Galaxy is utilizing infrastructure generously provided by the Texas Advanced Computing Center. Additional resources are provided primarily on the Jetstream2 cloud via ACCESS, and with support from the National Science Foundation. Quantify, visualize, and summarize mismatches in deep sequencing data. Build maximum-likelihood phylogenetic trees. Phylogenomic/evolutionary tree construction from multiple sequences. Merge matching reads into clusters with TN-93. Remove sequences from a reference that are within a given distance of a cluster. Perform maximum-likelihood estimation of gene essentiality scores.
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    Geneious

    Geneious

    Geneious

    Geneious Prime makes bioinformatics accessible by transforming raw data into visualizations that make sequence analysis intuitive and user-friendly. Simple sequence assembly and easy editing of contigs. Automatic annotation for gene prediction, motifs, translation, and variant calling. Genotype microsatellite traces with automated ladder fitting and peak calling and generates tables of alleles. Beautiful visualizations of annotated genomes and assemblies are displayed in a highly customizable sequence view. Powerful SNP variants analysis, simple RNA-Seq expression analysis, and amplicon metagenomics. Design and test PCR and sequencing primers and create your own searchable primer database. Geneious Biologics is a flexible, scalable, and secure way to streamline your antibody analysis workflows, create high-quality libraries and select the optimal therapeutic candidates.
    Starting Price: $1,280 per year
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    Cosmas

    Cosmas

    MAK-SYSTEM

    Connecting patients, clinicians, hospitals, and manufacturers in a single patient-centric platform for tissue, cell, and gene therapy. Digital orchestration of advanced therapies and the complex supply chain for any human material. Flexible and scalable to meet the needs of small and large centers. From clinical trial to commercialization, Cosmas supports the traceability and management of your treatments across the complete supply chain. Manages chain of identity and chain of custody with real-time tracking of the products through a complex value chain, enabling safe and efficient treatment. Large catalog of interfaces with third-party software and lab devices available. We are a leading digital product for orchestrating advanced therapies and the complex supply chain for any human material. Cosmas will enable biotech/pharma to deliver the right dose to the right patient, and scale and optimize the personalized therapy digital landscape.
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    QIAGEN CLC Genomics Workbench

    QIAGEN CLC Genomics Workbench

    QIAGEN Digital Insights

    QIAGEN CLC Genomics Workbench is a powerful solution that works for everyone, no matter the workflow. Cutting-edge technology and unique features and algorithms widely used by scientific leaders in industry and academia make it easy to overcome challenges associated with data analysis. User-friendly bioinformatics software solutions allow for comprehensive analysis of your NGS data, including de novo assembly of whole genomes and transcriptomes, resequencing analysis (WGS, WES and targeted panel support), variant calling, RNA-seq, ChIP-seq and DNA methylation (bisulfite sequencing analysis). Analyze your RNA-seq and small RNA (miRNA, lncRNA) data with easy-to-use transcriptomics workflows for differential expression analysis at gene and transcript levels. QIAGEN CLC Genomics Workbench is developed to support a wide range of NGS bioinformatics applications.
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    StrandOmics

    StrandOmics

    Strand Life Sciences

    Efficient reporting of NGS-based clinical tests requires a robust and mature platform for automatic variant prioritization, clinical interpretation and report generation. Strand Omics is a fast, HIPAA-compliant cloud-based platform that drives our clinical diagnostics practice. It has been honed over 4 years and over 10,000 clinical reports and multiple peer-reviewed publications. Strand Omics combines bioinformatics algorithms, curated databases, visualization interfaces and reporting capabilities. It has specialized workflows for both rare inherited disorders as well as somatic tumor profiling tests. The platform contains over 10,000 somatic variants curated for oncogenicity, 100 genes curated for druggability in multiple cancer types and 500 drugs curated for evidence in multiple cancer types.
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    Geneyx

    Geneyx

    Geneyx

    Geneyx Analysis is a comprehensive solution for next-generation sequencing (NGS) data that can scale the process of FASTQ to clinical reports for hospital and commercial labs. This advanced platform integrates machine learning and AI-based features to identify novel biomedical insights, while also improving diagnostic yields and turnaround times. By providing a fully transparent and intuitive solution, Geneyx Analysis enables clinicians and researchers to have complete control over data analysis and alleviates the complexities of regulating in-house bioinformatics pipelines. Protocols can be fully customized to accommodate gene panels, exomes, and genomes, and our comprehensive annotation engine supports the analysis of all genetic variants including structural and copy number variations as well as regulatory elements. Together, Geneyx Analysis automates the diagnostic process from sequencer to report, while creating a comprehensive resource for novel variant discovery.
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    Jinni

    Jinni

    Jinni

    Jinni's taste-based content-to-audience platform provides revolutionary personalization solutions for video content discovery and targeted digital advertising for entertainment brands. Through its unique Entertainment Genome™, consisting of thousands of distinct content attributes or "genes", Jinni not only understands the most subtle differences in TV and movie entertainment content but also understands each individual's unique entertainment tastes, thereby providing the perfect match between individual and content titles! Our mission is to be the best-in-class content-to-audience platform for entertainment brands, using one platform to match & promote entertainment content to the right audiences, dramatically increasing profitability for platform operators and entertainment advertisers. Jinni's semantic algorithms that match content to users' personal tastes have been setting the direction for the next generation of content discovery & recommendations for the industry.
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    Artbreeder

    Artbreeder

    Artbreeder

    Make a simple collage from shapes and images, describe it with a prompt, and watch as Artbreeder brings it to life. Splicer lets you create images by mixing them together and editing their genes. Create portraits, landscapes, paintings, and more, then watch as others take your art in exciting new directions. Artbreeder brings creativity and collaboration together. Remix any image you see to make it your own. Follow your favorite creators and share your work with a vibrant AI art community. Whether it’s concept art, history, or music videos, artists are finding incredible ways to bring Artbreeder into their creative processes. Artbreeder aims to be a new type of creative tool that empowers users' creativity by making it easier to collaborate and explore. Originally Ganbreeder, it started as an experiment in using breeding and collaboration as methods of exploring high-complexity spaces. Artbreeder is named after the research of Picbreeder.
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    GenomeStudio
    Visualize and analyze data generated on Illumina array platforms with GenomeStudio Software. This powerful solution supports the genotyping analysis of microarray data. Performance-optimized tools and a user-friendly graphical interface enable you to convert data into meaningful results quickly and easily. Analyze SNP and CNV data across 5 million markers and probes. Detect sample outliers. Analyze differentially expressed genes across different genomes. Profile miRNA expression. Combine mRNA and microRNA data in a single project. Detect cytosine methylation at single-base resolution. Identify methylation signatures across the entire genome. At Illumina, our goal is to apply innovative technologies to the analysis of genetic variation and function, making studies possible that were not even imaginable just a few years ago. It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers.
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    SyncGene

    SyncGene

    SyncGene

    SyncGene synchronizes your data automatically*, so you can keep your Contacts and Calendar events in sync and up to date across all of your accounts. You just need to add at least 2 sources you want to sync (Google/Exchange/iCloud). The changes, which you make in one source, will be automatically transferred to another without any duplicates. You can share the latest information from your address book or calendar with other people. Merge your personal information from various places. We'll unify this information into one synced view of one Calendar, one Address Book and one To-do list for your hassle-free management. No more lost, duplicate or incomplete entries. Manage and update your events, contacts and tasks from any connected device, service or app.
    Starting Price: $5.83 per month
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    ndCurveMaster

    ndCurveMaster

    SigmaLab Tomas Cepowski

    ndCurveMaster is a specialized software designed for multivariable curve fitting. It automatically applies nonlinear regression equations to your datasets, which can consist of observed or measured values. The software supports curve and surface fitting in 2D, 3D, 4D, 5D, ..., nD dimensions. This means that no matter how complex your data is or how many variables it has, ndCurveMaster can handle it with ease. For example, ndCurveMaster can efficiently derive an optimal equation for a dataset with six inputs (x1 to x6) and an output Y, such as: Y = a0 + a1 · exp(x1)^-0.5 + a2 · ln(x2)^8 + ... + a6 · x6^5.2, to accurately match measured values. Utilizing machine learning numerical methods, ndCurveMaster automatically fits the most suitable nonlinear regression functions to your dataset and discovers the relationships between the inputs and output. This robust tool offers linear, polynomial, and nonlinear curve fitting, utilizes crucial validation and goodness-of-fit tests.
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    Jeeva eClinical Cloud

    Jeeva eClinical Cloud

    Jeeva Informatics Solutions

    Jeeva's patent-pending modular solution is designed from the ground up on the most powerful cloud platform with one login from any browser-enabled mobile device for remote patient screening, education, enrollment, electronic informed consent, bi-directional communications via video calling, telemedicine, SMS, email, and evidence generation including electronic patient-reported outcomes and clinical outcomes assessments, with a modern user experience. Delays in patient recruitment & retention are keeping them up at night. Generating enough evidence of safety and efficacy of investigational new medicines is critical to get timely approval from regulatory agencies. Whether you are a patient group setting up a registry or natural history study, or a biopharma sponsor of a clinical trial, or a long-term follow-up study for gene therapy, Jeeva can save you time, and money while improving user experience for study team and trial participants.
    Starting Price: $100/mo/user
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    NLREG

    NLREG

    NLREG

    NLREG is a powerful statistical analysis program that performs linear and nonlinear regression analysis, surface and curve fitting. NLREG determines the values of parameters for an equation, whose form you specify, that cause the equation to best fit a set of data values. NLREG can handle linear, polynomial, exponential, logistic, periodic, and general nonlinear functions. Unlike many "nonlinear" regression programs that can only handle a limited set of function forms, NLREG can handle essentially any function whose form you can specify algebraically. NLREG features a full programming language with a syntax similar to C for specifying the function that is to be fitted to the data. This allows you to compute intermediate work variables, use conditionals, and even iterate in loops. With NLREG it is easy to construct piecewise functions that change form over different domains. Since the NLREG language includes arrays, you can even use tabular look-up methods to define the function.
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    Hippocrate

    Hippocrate

    HIPPOCRATE

    Engage, Diagnose, Prescribe and improve Patient Experience, Satisfaction and loyalty through a Patient-Centric Approach to Medicine. Get access to more Patients and increase your profitability while decreasing your costs! Connect, Discuss, Refer a Patient securely and Present your toughest cases to colleagues. Collaborate with other Medical specialists and share your knowledge and experience, in our fully encrypted smart Medical Social Network. A Highly Secure and Scalable Big Data Health Platform, designed for Medical Researchers. Play with our anonymized Health data, MRT, fMRI, Genes, discover behind patterns and improve Patients Treatments with Big Data and Analytics! Hippocrates was selected to present the Best Big Data Health platform in the most prestigious Medical University in the world: Stanford Medical School. We introduced our new research in Health Care Systems and Medical Technology and explained how our solutions can revolutionize the Medical Field at no cost.
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    NLMatics

    NLMatics

    NLMatics

    Easiest way to extract data points from unstructured text. Simultaneously search through research reports, prospectus, customer requests or feedback to extract, track and analyze meaningful, custom defined data points. Access 100+ unique data points for your investment & risk management strategy. Search and create custom data sets from EDGAR and other public or private sources. Streamline your deal underwriting process. Streamline your capital markets and structured finance legal flow. Instantly extract 100+ data points to categorize, compare and collaborate with your clients. Deconstruct unstructured text in PubMed and clinical trial data into diseases, genes, proteins, symptoms & more. Get all your research in a single place. Bring in research from any source into your workspaces using our Chrome plug-in. Make digital PDFs to machine readable. JSON and HTML output with detailed section hierarchy, multi-level tables, lists, header, footer and watermarks removed.
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    Analyse-it

    Analyse-it

    Analyse-it Software

    The powerful statistical modelling & analysis you'd expect from an expensive statistics package. Includes multiple regression & model-fitting, ANOVA, ANCOVA, multiple comparisons, principal component analysis (PCA), factor analysis & hypothesis testing and other tools for exploratory data analysis. Statistical process control and quality improvement tools to meet customer expectations and keep them satisfied. Meet regulatory compliance demands with analytical and diagnostic method validation and verification. All the power of Analyse-it, combining all the features of the other editions. We've developed statistical software for more than 25 years, have a reputation for high-quality software, and have worked worked with some large companies on the back of that solid reputation.
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    IBM SPSS Amos
    IBM® SPSS® Amos is a powerful structural equation modeling (SEM) software that helps support your research and theories by extending standard multivariate analysis methods, including regression, factor analysis, correlation, and analysis of variance. Build attitudinal and behavioral models reflecting complex relationships more accurately than with standard multivariate statistics techniques using either an intuitive graphical or programmatic user interface. Amos is included in the Premium edition of SPSS Statistics (except in the campus edition, where it is sold separately). You can also buy Amos as part of the base, standard and professional editions of SPSS Statistics, or separately as a stand-alone application.
    Starting Price: $3,830 per user per month
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    Plug&Score Modeler
    An extremely easy-to-use scoring system. A tool created by scoring experts for small and medium size credit organizations. Exactly what you need for accurate real-time scoring (and only for scoring) without obsolete hard-to-learn features. The best cost to value ratio on the market. Up and running within a few days. Easy to use due to its wizard-based scorecard modeling interface. Monitor and validate scorecards using a set of pre-defined reports. Reject Inference with automated and manual inference methods. Automated binning based on chi-square and manual binning based on WOE. Automatic and manual sampling. Graphical statistics. Portfolio data filtering, sorting and re-assignment to “Good” and “Bad”. Transformation of numeric variables into categorical ones. Correlation coefficients (correlation coefficient is provided for each pair of variables for the dataset before and after the binning procedure).
    Starting Price: $9950 one-time payment
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    SmartstatXL

    SmartstatXL

    Smartstat

    SmartstatXL: Powerful Statistical Analysis Right in Excel. Unlock the full potential of your data with SmartstatXL, the Excel add-in that integrates advanced statistical analysis seamlessly into your familiar spreadsheet environment. This tool is designed to simplify your data analysis process by combining the robust capabilities of statistical software with the accessibility of Excel. Key Features of SmartstatXL: • Full Excel Integration: Perform sophisticated data analyses directly within Excel. SmartstatXL's integration allows you to leverage Excel's functionality alongside advanced statistical tools without switching between applications. • Extensive Analytical Tools: Equipped with a wide array of features, SmartstatXL offers everything from Descriptive Statistics, Normality Tests, and Hypothesis Tests (including t-Tests and z-Tests) to more complex analyses such as Correlation, Regression, ANOVA, Time Series, Reliability Assessments, Factor Analysis, PCA, Discriminant Analysis
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    Number Analytics

    Number Analytics

    Number Analytics LLC

    Number Analytics is a web based statistical software for marketing research with easy to use interface working on the cloud. It has basic statistical analysis like t-test, ANOVA, regression analysis, and more marketing focused applications like choice based conjoint analysis and perceptual mapping.
    Starting Price: $29.00/month/user