Alternatives to Sano

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

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    Apex LIS

    Apex LIS

    Apex Healthware, LLC

    Affordable Cloud-based LIS. Perfect for startup labs! Subscriptions start at $250/month including 3 analyzer interfaces unlimited users. CLIA-compliance suite makes it easy to comply with regulatory requirements. Easy-to-use application can be installed in a day and web-training available. LIS is easily configured to meet your exact analyzer and workflow requirements. HIPAA-compliant Phone app supports patient registration, test order and results notification. We have more than 300 deployments with clients specializing in: Fertility, Genetic testing, molecular testing, Pathology, Toxicology and virtually all other specialties. We have interfaced over 250 different analyzers including interfaces to the leading analyzers in the fields of molecular biology and genetic testing.
    Starting Price: $1500 one-time payment
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    Castor EDC
    Castor is a leading platform for clinical data management, offering advanced solutions for electronic data capture (EDC), patient-reported outcomes (ePRO), and eConsent. Designed to streamline clinical trials, Castor enables researchers to efficiently collect and manage data from multiple sources in a compliant, user-friendly environment. The platform also supports decentralized trials (DCTs), providing tools for remote patient recruitment, monitoring, and real-time data analysis. Castor is trusted by over 50,000 users globally, helping clinical research teams accelerate trials while ensuring high-quality data and regulatory compliance.
    Starting Price: $100.00/year
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    OpenClinica

    OpenClinica

    OpenClinica

    OpenClinica is a leading provider of clinical trial technology, offering a comprehensive suite of solutions to enhance the efficiency and effectiveness of clinical research. The platform provides electronic data capture (EDC), patient recruitment, eConsent, and clinical data management solutions, all designed to streamline workflows and improve data quality. OpenClinica also integrates EHR-to-EDC connectivity, allowing for seamless data acquisition and reducing errors. Trusted by life sciences companies, academic institutions, and government agencies, OpenClinica supports over 15,000 studies and has helped manage data for more than three million patients worldwide.
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    2bPrecise

    2bPrecise

    2bPrecise

    2bPrecise delivers transformative point-of-care solutions that serve as the foundation for scalable precision medicine success. Patient not responding to first-line treatments for common conditions? Pharmacogenomics helps you identify medications that are safer and more effective. Fingertip access to test results helps eliminate “trial-and-error” prescribing practices, and accelerates patient response. Detailed genetics-focused data-gathering tools help you capture and expose risk. In-workflow Pedigree visualization allows you to identify candidates that could benefit from genetic testing, and lead you to the best course of treatment. Patient presents you with a diagnostic dilemma (e.g., symptoms such as seizures or syncope correlated with multiple conditions)? Germline tests hone in on heritable factors that can inform diagnoses. Access to meaningful and actionable results during clinical decision-making enables you to initiate preventive measures.
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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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    Progeny Clinical

    Progeny Clinical

    Progeny Software

    See our quick screening tools to identify high-risk patients for breast, colorectal and other cancers. Progeny Clinical simplifies the process of managing family history, assessing risk and determining treatment options for your patients. Obtain family history data from patients online and auto-generate pedigrees before the clinic visit. Edit or create new pedigrees anytime. Run validated hereditary cancer risk assessment models at the touch of a button without re-entering data. Save time by ordering genetic testing from Ambry Genetics. Track and review results from any lab without ever leaving the software. Save time - create letters, consult notes, reports, and documents from custom templates that include patient data fields. Use pre-configured or custom data entry screens and quickly generate custom queries and spreadsheet reports. Add a hyperlink within your electronic medical record to easily display the patient’s most recent pedigree.
    Starting Price: $1600 one-time payment
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    Genomenon

    Genomenon

    Genomenon

    Pharma companies need comprehensive genomic information to drive successful precision medicine programs, but decisions are often made using only a fraction of the data available, about 10%. Genomenon delivers 100% of the data. An efficient and cost-effective natural history research solution for pharma, ProdigyTM Patient Landscapes support the development of rare disease therapies by enhancing insights contained in retrospective and prospective health data. Using a powerful AI-driven approach, Genomenon delivers a comprehensive and expert assessment of every patient in the published medical literature, in a fraction of the time. Don’t miss anything, get insight into every genomic biomarker published in the medical literature. Every scientific assertion is supported by empirical evidence from the medical literature. Identify all genetic drivers and pinpoint which variants are known to be pathogenic according to ACMG clinical standards.
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    SOPHiA GENETICS

    SOPHiA GENETICS

    SOPHiA GENETICS

    Our global data-sharing network generates clinically actionable insights from data to improve patient outcomes worldwide. SOPHiA GENETICS’ mission is to build the future of AI-assisted medicine. We are integrating multimodal healthcare-omics data, unlocking the existing data silos, and developing machine learning models to produce actionable insights that could eventually support healthcare professionals to improve patient outcomes. The revamped interface, new features, and cutting-edge capabilities are set to further accelerate precision medicine workflows, bringing us another step closer to democratizing data-driven medicine.​ Powered by AI and machine learning (ML), our global cloud-based platform provides a safe, secure, and instantly accessible environment to standardize, compute, and analyze digital health data, generating insights from complex multimodal data sets that have the potential to improve diagnosis, therapy selection, analysis, and drug development.
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    Breeders Assistant
    Breeders Assistant (BA) is a specialist animal pedigree, record-keeping, and genetics analysis application for Windows 10 and Windows 11. At its simplest, it is used to produce high-quality pedigree certificates and store all breeding records in a private pedigree database held locally on your computer. BA has many advanced genetic features, including very fast inbreeding calculations. With the extended edition, it can prioritize prospective matings in a number of ways to minimize the inbreeding that would result from the mating, to maximize the influence of specific individuals within the breeding population, or to minimize the loss of genetic diversity by minimizing mean kinship. BA is supplied in several versions carefully tailored for the specific needs of breeders of pedigree cats, dogs, horses, and many other species. There is also a generic version that can be used for any animal type where a specific custom version is not provided.
    Starting Price: $125.91 one-time payment
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    OmicsBox

    OmicsBox

    BioBam Bioinformatics S.L.

    OmicsBox is a leading bioinformatics solution that offers end-to-end data analysis of genomes, transcriptomes, metagenomes, and genetic variation studies. The application is used by top private and public research institutions worldwide and allows researchers to easily process large and complex data sets, and streamline their analysis process. It is designed to be user-friendly, efficient, and with a powerful set of tools to extract biological insights from omics data. The software is structured in different modules, each with a specific set of tools and functions designed to perform different types of analysis, such as de-novo genome assemblies, genetic variation analysis, differential expression analysis, and taxonomic classifications of microbiome data, including the functional interpretation and rich visualizations of results. The functional analysis module includes the popular Blast2GO annotation methodology and makes OmicsBox particularly suited for non-model organism research
    Starting Price: €100/month/seat
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    RAMAS IRM
    RAMAS® IRM (Insect Resistance Management) is a software platform for modeling the risk of pest adaptation to Bt crops under a broad range of resistance management strategies. The tool has enough flexibility to address all major insect crop pests through user-defined life histories. IRM modeling investigates the complex interaction of insect pest population dynamics and population genetics with agricultural technology and farming practices. The total integration of landscape, demography, and evolution places IRM at the cutting edge of landscape genetics and applied evolution. Our goal is to provide a common platform for IRM modeling that fosters both transparency and innovation in the development and management of transgenic pesticidal crops. A guiding principle in the development of this flexible tool is that it should remove barriers to powerful modeling.
    Starting Price: $200 per 6 months
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    VSClinical

    VSClinical

    Golden Helix

    VSClinical allows for the clinical interpretation of variants based on ACMG & AMP guidelines. The VSClinical guided workflow enables following the American College of Medical Genetics (ACMG) guidelines used to identify and classify causal variants for inherited disease risk, cancer predisposition, and the diagnosis of rare diseases. The ACMG/AMP joint guidelines for variant interpretation provide a set of criteria to score variants and place them into one of five classification tiers. Following the guidelines requires deep diving into the annotations, genomic context, and existing clinical assertions about every variant. VSClinical provides a tailored workflow to score each relevant criterion while also providing all the bioinformatic, literature and evidence from clinical knowledgebases to assist in the scoring and interpretation process. VSClinical is designed to allow variant scientists to efficiently process variants.
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    american fuzzy lop
    American fuzzy lop is a security-oriented fuzzer that employs a novel type of compile-time instrumentation and genetic algorithms to automatically discover clean, interesting test cases that trigger new internal states in the targeted binary. This substantially improves the functional coverage for the fuzzed code. The compact synthesized corpora produced by the tool are also useful for seeding other, more labor or resource-intensive testing regimes down the road. Compared to other instrumented fuzzers, afl-fuzz is designed to be practical, it has a modest performance overhead, uses a variety of highly effective fuzzing strategies and effort minimization tricks, requires essentially no configuration, and seamlessly handles complex, real-world use cases, say, common image parsing or file compression libraries. It's an instrumentation-guided genetic fuzzer capable of synthesizing complex file semantics in a wide range of non-trivial targets.
    Starting Price: Free
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    Genome Computer

    Genome Computer

    Genome Computer

    Genome Computer turns your genetic data into a portable, AI-ready .genome bundle you can download, keep, self-host, and explore with Genome Intelligence, Codex, Claude Code, Cursor, or any compatible tool. The open format restructures the same underlying data found in a VCF into a structured, queryable bundle, with variants stored in fast columnar tables alongside trait associations, supporting research, gene-level context, polygenic scores, pharmacogenomics, and clear provenance. Whole-genome sequencing orders are built from gVCF data, preserving both detected variants and confidently sequenced regions where no variant was found, while FASTQ files are available on request. Existing VCF or TXT files from other providers can also be converted, imputed where needed, annotated, scored, and prepared for AI interpretation. Genome Intelligence lets you ask questions grounded in your actual genetic data, compare new research with your genotypes, and explore genetics.
    Starting Price: $15 per month
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    Volpara Health

    Volpara Health

    Volpara Health

    Facilities use Volpara Health software for early detection of breast cancer, including top US cancer screening centers. Mammography technologists rely on Volpara Health to improve mammogram quality. The most scientifically validated screening software in the breast health industry. Volpara gives you the evidence you need, right when you need it. Access to patient data for more informed breast cancer risk assessment. Each and every image we analyze improves our algorithms for early detection of breast cancer. Your aid in advocating for additional screening or genetic testing of patients. Build worklists and reports to individual preferences. Simultaneously access stats and lists from a single screen. Standardize communications for patients, referrers, and insurers. Send more compelling result letters with mammogram thumbnail images.
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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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    BreederHQ

    BreederHQ

    BreederHQ

    BreederHQ is a cloud-based breeding program management platform for dogs, cats, horses, goats, sheep, and rabbits. It replaces spreadsheets and disconnected tools with one integrated system. Core features include detailed animal profiles with health records, registries, and genetic test imports (Embark, Etalon, UC Davis); a genetics lab with species-specific analysis (up to 35+ loci), Punnett squares, offspring simulation, and coat color prediction; full breeding lifecycle management with heat cycle projection, visual calendars, and Gantt timelines; offspring tracking with neonatal care, rearing protocols, and digital completion certificates; a buyer CRM with Kanban sales pipeline, lead scoring, and waitlist matching; dual-mode invoicing (manual or Stripe), expense tracking, and contracts with e-signatures; a verified marketplace for breeder discovery with trust badges; a client portal for buyers; and iOS/Android mobile apps. Supports 583 breeds across 40+ registries, 5 languages
    Starting Price: $29/month
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    TPIL Genetics™
    TPIL Genetics™ is an AI-powered, end-to-end transfer pricing platform used by corporates globally to simplify, strengthen and scale compliance in a more efficient and cost-effective way. Built to be industry-agnostic, it brings consistency across transfer pricing policy, implementation and documentation through one centralised ecosystem. The platform streamlines data collection, automates TP calendars and workflows, supports real-time management of intercompany policies, and delivers defensible benchmarking, Pillar Two readiness and global compliance. It produces complete three-tier documentation, supports jurisdiction-specific disclosures, and enables localisation in English and additional local languages. With integrated knowledge management, audit trails and collaboration tools, TPIL Genetics™ helps multinational groups reduce risk, improve transparency and achieve audit-ready compliance across all entities and jurisdictions.
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    BioSymetrics

    BioSymetrics

    BioSymetrics

    We integrate clinical and experimental data using machine learning to navigate human disease biology and advance precision medicines. Our patent-pending Contingent AI™ understands relationships within the data to provide sophisticated insights. We address data bias by iterating on machine learning models based upon decisions made in the pre-processing and feature engineering stages. We leverage zebrafish, cellular and other phenotypic animal models to validate in silico predictions in vivo experiments and genetically modify them in vitro and in vivo, to improve translation. Using active learning and computer vision on validated models for cardiac, central nervous system and rare disorders, we rapidly incorporate new data into our machine learning models.
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    Genoox

    Genoox

    Genoox

    Through our diverse and growing community, Genoox accumulates the most relevant database and delivers actionable, real-world genomic insights that impact lives, improve clinical outcomes, and shape the business of healthcare. Our solutions are changing the face of genomics. Genoox uses the power of its community and combines public data with community data to streamline the path from DNA sample to clinical report, impacting patient care by making genomic data accessible and actionable at the point of care. Genoox enhances research and life sciences companies by providing an insight platform derived from real-world data and evidence and powered by our community with robust genomic analytics, helping researchers simplify complex genomic data and make impactful discoveries using the most advanced genetic tools and applications. Genoox helps biosystems companies such as DNA sequencing companies to bundle its state-of-the-art genomic engine with dedicated assays.
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    Optitravel

    Optitravel

    Optigest

    Values such as ethics, rigor and requirement are part of Optigest genetic code. Company founded with the aim of being the preferred partner of the tourism actors and specialized in this field being his main focus. To implement a technological system that responds directly to customer needs is necessary a thorough knowledge of the operation, difficulties and needs. The close cooperation with the customers in the form of partnership is a model used by Optigest. The Optitravel – Travel Agency Manager allows you to manage on a easy way all processes of your agency, from customer management integration with accounting, anywhere in the world with secure internet access.
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    MEGA

    MEGA

    MEGA

    MEGA (Molecular Evolutionary Genetics Analysis) is a powerful and user-friendly software suite designed for analyzing DNA and protein sequence data from species and populations. It facilitates both automatic and manual sequence alignment, phylogenetic tree inference, and evolutionary hypothesis testing. MEGA supports a variety of statistical methods including maximum likelihood, Bayesian inference, and ordinary least squares, making it an essential tool for comparative sequence analysis and understanding molecular evolution. MEGA offers advanced features such as real-time caption generation to help explain the results and methods used in analysis and the maximum composite likelihood method for estimating evolutionary distances. The software is equipped with robust visual tools like the alignment/trace editor and tree explorer and supports multi-threading for efficient processing. MEGA can be run on multiple operating systems, including Windows, Linux, and macOS.
    Starting Price: Free
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    Seegnal

    Seegnal

    Seegnal

    Intuitive user interface at the point of care, in real time. A smart patient-specific platform for preventing Drug-Related Problems (DRPs). DRPs are the 4th leading cause of mortality in the US, resulting in approximately 150,000 deaths annually. DRPs are responsible for 6-10% of hospital admissions. Over 20% of patients who receive 5 concomitant medications (or more) are susceptible to severe DRPs DRPs cause billions of dollars in wasted expenditure. DRPs cause 4.5 million Americans to visit hospital emergency rooms every month. Widest scope of data. 50% additional exclusive data. Multi-source synchronization. AI/ML Patient specific. Real time patient modifiers (lab results, eGFR, etc.) Patient’s genetics, nutrition, OTC. Groundbreaking accuracy. 98% accuracy – specificity & sensitivity. No alert-fatigue. Only 6% alerting vs. legacy systems. Patented visualization at the point of care. 5-10 seconds to detect, prioritize and resolve.
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    LabData LIMS

    LabData LIMS

    Solutions Orange Data

    Our LIMS adapt to your technical, quality and administrative requirements. Through our services we can complement any need. Get great added value at no cost. LIMS specific for physical, chemical, microbiological, environmental, agronomic testing laboratories . LIMS specific for integrated laboratories in industries. LIMS specific for genetics and / or molecular biology laboratories. LIMS specific for clinical analysis laboratories. LIMS specific for research laboratories. Specific software for pathological anatomy laboratories. Beyond analytical management and production, with our tools you can cover a specific part of your procedures in your laboratory. Get higher quality and speed of work in other areas. Web platform for consulting analytics, results and reports. Platform for tablets and mobiles for the management of analytics, introduction of results, collection of samples. Software for quality management in laboratories, complying with ISO 17.025 and 9001 procedures.
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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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    Build Alpha

    Build Alpha

    Axiom Futures

    Build Alpha uses a genetic algorithm to create thousands of algorithmic trading strategies at the click of a button. Combine, test and create millions of entry and exit signals with no coding necessary. Find complimentary filters to existing rules, improve existing strategies or create new ones. Ability to backtest, stress test and generate code from one algorithmic trading software with no code. Data included and partnered with various data providers and brokers. Build Alpha also generates complete code for multiple trading brokers such as: TradeStation, MultiCharts, NinjaTrader, MetaTrader4, MetaTrader5, Python and more. All asset classes, timeframes and bar types.
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    Starting Price: $1500 one-time
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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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    MultiCharts

    MultiCharts

    MultiCharts

    Freedom of choice has been the driving idea behind our MultiCharts and you can see it in the wide choice of supported data feeds and brokers. Choose your trading method, test it, and start trading with any supported broker you like — that’s the advantage of MultiCharts. Whether you need day trading software or you invest for longer periods, MultiCharts has features that may help achieve your trading goals. High-definition charting, built-in indicators and strategies, one-click trading from chart and DOM, high-precision backtesting, brute-force and genetic optimization, automated execution and support for EasyLanguage scripts are all key tools at your disposal.
    Starting Price: $97 per month
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    Fido

    Fido

    Fido

    Fido is a light-weight, open-source, and highly modular C++ machine learning library. The library is targeted towards embedded electronics and robotics. Fido includes implementations of trainable neural networks, reinforcement learning methods, genetic algorithms, and a full-fledged robotic simulator. Fido also comes packaged with a human-trainable robot control system as described in Truell and Gruenstein. While the simulator is not in the most recent release, it can be found for experimentation on the simulator branch.
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    HeartFlow

    HeartFlow

    HeartFlow

    HeartFlow's non-invasive personalized cardiac test provides unprecedented visualization of each patient's coronary arteries, enabling physicians to create more effective treatment plans for their patients. The HeartFlow FFRCT Analysis starts when a patient undergoes a standard coronary computed tomography scan at a hospital or imaging center. The CT images are securely uploaded to our cloud. Next, we use advanced algorithms incorporating artificial intelligence to build a personalized, digital model of that patient’s coronary arteries. Our team of highly trained analysts then inspects this model, making any needed edits. Once this patient-specific model is completed, the HeartFlow pathway applies physiologic principles and computational fluid dynamics to compute the blood flow and FFRCT values at every point in the model. Throughout the process, we follow rigorous and well-established protocols to ensure consistent processing for every patient.
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    Altis Labs Nota
    Altis Labs announces launch of Nota – a clinical information platform to accelerate therapeutic R&D Nota leverages. AI to predict patient outcomes from imaging data so sponsors can better prioritize their most promising therapies. Nota enables researchers to operationalize clinical trial imaging data, access predictive imaging biomarkers, and accelerate R&D at scale. Using Altis’ cloud-based software platform powered by deep learning, biopharma can incorporate comprehensive outcome predictions at the image, patient, and cohort level to improve clinical trial design and more confidently anticipate clinical endpoints. Such insights have the potential to significantly accelerate development timelines, lower drug development costs, and improve the likelihood of trial success across therapeutic areas.
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    Leapcure

    Leapcure

    Leapcure

    Leapcure is a leading patient recruitment and engagement platform that connects clinical trial sponsors with eligible patients. Utilizing advanced technology and strategies, we enhance trial participation and improve patient outcomes. Our platform streamlines the recruitment process, ensuring that trials are populated with suitable candidates quickly and efficiently. Leapcure is dedicated to advancing medical research by making clinical trials more accessible and effective. We work closely with sponsors and patients to facilitate smooth and successful trial experiences, ultimately contributing to the development of new treatments and therapies.
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    Kinvara

    Kinvara

    Kinvara

    Kinvara is all-in-one breeder software for dog breeders and catteries, replacing the spreadsheets, paper folders and text threads a breeding program usually runs on. Track every dog or cat with photos, titles, registrations, health testing and a multi-generation pedigree. Plan pairings with genetics forecasts, log litters, and record per-puppy weights, vaccinations and temperament tests. Applications flow in from your existing website and join the right waitlist in deposit order. Every buyer family gets a private portal: photos as their animal grows, health records, an e-signable contract and online payment. Invoices are paid through your own payment account, so the money lands with you and Kinvara never holds your funds. Catteries are native, not an afterthought: every screen, email and document speaks cattery, with TICA/CFA registries.
    Starting Price: $39/month
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    KoolPerform

    KoolPerform

    Sapien Technology

    KoolPerform provides detailed data analysis, reporting and sharing capabilities. Bullet point Interface with breed societies, Breedplan and Sheep Genetics Australia. Bullet point Filter and sort for advanced data analysis. Bullet point Extensive standard and custom reporting options. KoolPerform is designed for seedstock producers, with KoolPerform you can identify lists of animals based on any information you have previously collected. Produce detailed reports on your animals and get full use out of the data you collect.
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    Superpower

    Superpower

    Superpower

    Superpower is a comprehensive digital health platform designed to help individuals live longer, prevent disease, and optimize their well-being. By combining whole-body testing with personalized health programs, Superpower provides members with an all-in-one health membership that includes testing for hormones, thyroid function, heart health, toxins, genetics, microbiome, cancer risk, and more. Members receive an annual roadmap detailing actionable steps to enhance various aspects of their health, transitioning from uncertainty to control. The platform offers access to a private concierge clinician, enabling members to communicate via text for assistance with orders, scheduling, questions, and coaching. Superpower also features a curated marketplace of health products, tests, and services at insider prices, with new additions weekly. Personalized programs target areas such as gut health, hormone optimization, aging, toxin exposure, disease risk, body composition, etc.
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    Artemis

    Artemis

    TurinTech AI

    Artemis leverages Generative AI, multi-agent collaboration, genetic optimization, and contextual insights to analyze, optimize, and validate codebases at scale, transforming existing repositories into production-ready solutions that improve performance, reduce technical debt, and ensure enterprise-quality outcomes. Integrating seamlessly with your tools and repositories, it uses advanced indexing and scoring to pinpoint optimization opportunities, orchestrates multiple LLMs and proprietary algorithms to generate tailored improvements, and performs real-time validation and benchmarking to guarantee secure, scalable results. A modular Intelligence Engine powers extensions for profilers and security tools, ML models for anomaly detection, and an evaluation suite for rigorous testing, all designed to lower costs, boost innovation, and accelerate time-to-market without disrupting existing workflows.
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    IAL (InterActive Lab)

    IAL (InterActive Lab)

    Interactive Technology Services

    IAL (Interactive lab) Platform is modular platform which enables labs to manage samples end to end workflow. IAL is a Laboratory information System (LIS / LIMS) which is a web based application system that empowers your testing facility with the ability to improve efficiency, better manage samples and test results, and automate workflows and associated information. The IAL platform is modular with each module to fit in lab operation workflow. IAL is the best solution for managing your molecular diagnostics and genetic testing lab. Secure and HIPAA compliance Works with a wide range of testing systems and high complexity analyzers Interfaces with wide range of healthcare systems. Web-based access, order entry, test scheduling, and results queries Modular, you can choose the modules to fit your custom lab workflow to enhance your operations scalability Customizable Exportable Views through dynamic grid Can be hosted in our cloud or on your servers. Custom Reporting.
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    SwimScore

    SwimScore

    SwimScore

    SwimScore is a modern platform for male reproductive health testing designed for clinics and healthcare providers. It offers lab-grade semen analysis with up to 21 clinically relevant parameters. The platform supports at-home sample collection when appropriate, improving patient comfort and compliance. SwimScore also includes optional hormone testing, such as testosterone, FSH, and LH levels. It provides advanced sperm quality analysis, including DNA fragmentation testing. Clinics benefit from automated tracking, result delivery, and reduced need for in-office sample handling. A centralized portal gives providers real-time visibility into patient testing and results. By combining diagnostics with streamlined workflows, SwimScore enhances both patient experience and clinical efficiency.
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    OneStudyTeam

    OneStudyTeam

    Reify Health

    We build solutions that connect and empower the clinical trial ecosystem. The Enrollment Performance Management platform that sites love and sponsors depend on. Used by 2,000 research sites across 26 countries and by half of the top-20 global biopharma companies. Sites spend less time with redundant and manual tasks so that they can move patients forward. Less double work for sites. Fewer logs, phone calls, and emails for both sites and sponsors. Sponsors can optimize enrollment proactively with real-time access to novel pre-screening and enrollment data. Surprisingly simple patient recruitment and enrollment solution trusted by more than 1,800 sites across 26 countries. Access powerful recruitment and enrollment insights to run faster, more predictable clinical trials. Eliminate redundant work so you can get back to the work that matters most: helping patients. Manage recruitment across all trials, sponsors, or CROs. Enter information once and it goes where you need it to go.
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    Advanced Human Imaging

    Advanced Human Imaging

    Advanced Human Imaging

    Advanced Health Intelligence (AHI) offers digital biomarker-derived health risk assessments, enabling proactive risk management for global populations through user-friendly, smartphone-based solutions. Our digital health Assessment provides comprehensive insights into cardiovascular, metabolic, and mental health risks. FaceScan delivers health vital estimates via the web or smartphone using camera-sensor inputs in around two minutes. BodyScan allows users to self-assess body composition and dimensions, along with associated health risks, in comfort and privacy. AHI's solutions offer population risk stratification, greater access to prevention support, contactless and non-invasive risk assessment, digital biomarker underwriting, convenient self-administration, and engagement with remote populations. Our unique portfolio of healthcare technologies holds patents across many countries.
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    PacBio

    PacBio

    Pacific Biosciences (PacBio)

    PacBio (Pacific Biosciences) is a premier life science technology company that is designing, developing and manufacturing advanced sequencing solutions to help scientists and clinical researchers resolve genetically complex problems. Our products and technologies stem from two highly differentiated core technologies focused on accuracy, quality and completeness which include our HiFi long-read sequencing and our SBB® short-read sequencing technologies. Our products address solutions across a broad set of research applications including human germline sequencing, plant and animal sciences, infectious disease and microbiology, oncology, and other emerging applications. The Revio system adds affordability, high throughput, and ease of use to a foundation of long reads, exceptional accuracy, and direct methylation detection. The Onso system is an innovative benchtop short-read DNA sequencing platform with an extraordinary level of accuracy using PacBio sequencing by binding.
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    AForge.NET

    AForge.NET

    AForge.NET

    AForge.NET is an open source C# framework designed for developers and researchers in the fields of Computer Vision and Artificial Intelligence - image processing, neural networks, genetic algorithms, fuzzy logic, machine learning, robotics, etc. The work on the framework's improvement is in constants progress, what means that new feature and namespaces are coming constantly. To get knowledge about its progress you may track source repository's log or visit project discussion group to get the latest information about it. The framework is provided not only with different libraries and their sources, but with many sample applications, which demonstrate the use of this framework, and with documentation help files, which are provided in HTML Help format.
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    Douyin

    Douyin

    Douyin

    Here, you can learn about the latest star content and events! The stars you like are all on Douyin! Smart matching of music, one-click video, and a lot of original special effects, filters, scene switching to help you become a blockbuster in one second, so that your life can be easily recorded on Douyin! Life coups, food practices, travel strategies, scientific and technological knowledge, news and current affairs, and city information, all the practical content you need is on Douyin! Original musicians, Peking opera actors, non-genetic inheritors, barbecue stall owners, courier brothers, etc., everyone's real life is in Douyin!
    Starting Price: Free
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    HEKMA

    HEKMA

    HEKMA

    HEKMA is an AI-powered clinical trial intelligence company focused on accelerating clinical research by improving patient recruitment, trial feasibility, and patient engagement. The company serves CROs, pharmaceutical sponsors, hospitals, and patients through an integrated platform that connects electronic health records (EHRs), AI-driven trial matching, clinical trial management, and patient engagement tools. Its mission is to reduce enrollment delays, improve access to clinical trials; particularly for underserved populations and make clinical research more efficient, transparent, and patient-centric. HEKMA combines expertise in healthcare, artificial intelligence, and clinical operations while maintaining compliance with industry standards such as HIPAA, 21 CFR Part 11, GDPR, and HL7/FHIR.
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    AI Jobs

    AI Jobs

    AI Jobs

    Strengthen your teams with the best AI professionals in France. Welcome to AI Jobs, the largest job site for finding and posting job offers in the field of artificial intelligence. AI Jobs is the only job site in France 100% dedicated to artificial intelligence. We federate a community of 19,000 standby professionals and specialized AI profiles in active search in order to push your offer to the right candidates. Each month, 1,200 companies such as Thales , Tinyclues, and Sophia Genetics trust us to recruit their specialized AI profiles in France. Artificial intelligence is arguably the most impactful disruption since the early days of the Internet. That's why we created AI Jobs. We thus enable companies to find the best talents to accelerate this revolution. Don't worry if everything isn't perfect the first time, it can be edited anytime after it's posted! Increase the visibility of your job offer thanks to a colored highlight ( +23% of applications ).
    Starting Price: €37 per ad
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    Genospace

    Genospace

    Genospace

    At Genospace, we understand that genomics is driving the development of precision medicine, yet scaling its delivery is an unsolved challenge. We’re here to help. Our platform is designed to make biomedical data meaningful and accessible to everyone, especially those on the front lines of care delivery. Arm your clinicians and researchers with the information they need to make informed decisions and join us in our mission of leveraging high-dimensional molecular data to improve individual patient outcomes and accelerate drug development and research. Large-scale population data is necessary for drug development and research. Conduct cohort-driven analyses to inform your research activities with the Genospace platform. We specialize in clinical trial research. Use the Genospace platform to match fragmented patient data to complex trial criteria and expedite patient accruals. Integrate genomic medicine into mainstream clinical care with the Genospace platform.
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    75health

    75health

    Kaaspro

    75Health is a cloud-based electronic health record (EHR) solution that helps medical professionals working in small and midsize medical clinics to manage patient information and digital records. Key features include a built-in scheduler, drug list management, automated email generation, a tracker for diagnostic tests, vaccination tracking and more. Users can upload and store patients' records and practice documents like consent forms, handouts, and x-rays. They can also scan records for allergies, medications, lab results and symptom lists and create patient care plans with tests and guidelines using the solution. 75Health features e-prescribing that enables professionals to submit electronic prescriptions and manage patient statements. The solution's clinical decision support gives clinicians information about patient allergies, the dosage of drugs and more. Reminders can also be sent to patients when their tests are overdue. 75Health offers support via email, phone and etc..
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    Signant Health

    Signant Health

    Signant Health

    Signant Health is a global evidence-generation company that helps modernize clinical trials by meeting patients where they are and reimagining the path to proof. They offer comprehensive clinical technology solutions, including electronic Clinical Outcome Assessments (eCOA), Electronic Data Capture (EDC), electronic clinician ratings, and a unified eClinical platform. Their patient engagement tools encompass a patient engagement app, eConsent, and telemedicine capabilities. Signant Health also provides clinical data and analytics services, such as COA data analytics and data aggregation and intelligence. With over 30 years of experience, they have supported thousands of trials and contributed to hundreds of drug approvals, making them a trusted partner for sponsors and CROs aiming to deliver high-quality data for trial decisions and regulatory submissions.
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    Elucid

    Elucid

    Elucid

    Deliver personalized patient care with the only histologically validated, objective, and quantitative CTA-based arterial analysis software. Utilize ground-truth histology to visualize the source of myocardial ischemia and inform heart attack and stroke risk. Heart attack and stroke are primarily caused by non-obstructive, but unstable plaque in the arteries that goes undiagnosed and untreated. Current non-invasive testing cannot visualize the biology deep inside artery walls where heart disease develops. Elucid is harnessing scientific imaging and artificial intelligence to enable quick, accurate, noninvasive diagnoses and precise treatment of cardiovascular disease to enable better patient outcomes. Assess plaque composition with histology-validated software. Quantify heart attack and stroke risk with greater accuracy. Visualize a comprehensive and objective view of arterial disease to enable personalized treatment plans before a patient ever enters the hospital.
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    LiveLink for MATLAB
    Seamlessly integrate COMSOL Multiphysics® with MATLAB® to extend your modeling with scripting programming in the MATLAB environment. LiveLink™ for MATLAB® allows you to utilize the full power of MATLAB and its toolboxes in preprocessing, model manipulation, and postprocessing. Enhance your in-house MATLAB code with powerful multiphysics simulations. Base your geometry modeling on probabilistic or image data. Use multiphysics models together with Monte Carlo simulations and genetic algorithms. Export COMSOL models on state-space matrix format for incorporating into control systems. Interface in the COMSOL Desktop® environment enables the use of MATLAB® functions while modeling. Manipulate your models from the command line or script to parameterize the geometry, physics, or the solution scheme.