This SaaS product offers high-throughput data processing pipelines for bioinformatics. It provides ready-to-use pipelines and infrastructure to process and analyze large datasets efficiently. Features include automatic data ingestion and enrichment, scalable resource management, and support for various data types like RNA-seq and LCMS.
Utilize production-ready bioinformatics pipelines to process a variety of multi-omics data types. These are scientifically validated and tailored to specific data types and analysis requirements.
Use Polly’s managed infrastructure to handle large datasets cost-effectively. Offers auto-scale resources based on usage and supports selecting computational resources for complex jobs.
Polly’s harmonization engine allows for large-scale data ingestion, transformation, and curation. It automates identifier mapping, quality checks, and more, while enforcing schema requirements.
Enhances the ability to integrate multi-modal datasets from diverse sources and ensure data quality through structured pipelines.
Ensures compliance with research standards, offering top-tier data quality for reliable research outcomes.
Allows you to tailor data curation processes according to specific project needs, supporting easy integration of various data forms.
Provides the infrastructure to handle high-speed and scale data processing, with support for large cohort analyses.
Streamline clinical trial data ingestion, curation, and sharing with data integration partners. Automatically annotates experiments with metadata for regulatory filing.
Supports R&D pipelines with cloud infrastructure. SOC2, PIPA, and CIPM certified to support data transfer.
Uses AI for interpreting historical omics data and contextualizing scientific findings.
Automates workflows and harmonizes data across workflows with DIY workflow setup.
Ensures high data accuracy through continuous quality checks.
Offers standardized data processing with harmonization pipelines.
Provides flexible deployment to suit data needs across platforms.
Facilitates requests for high-impact guides from public databases, ensuring relevant and licensed sources.
Experts analyze data needs, scout free and paid sources, and deliver curated data tailored to research purposes.
Supports access to over 32 data sources including GEO, Zendata, ArrayExpress, PRIDE, and others.
Offers scalable data harmonization to align diverse data sets for analysis.
Provides indication agnostic data handling, ensuring versatile application across different research needs.
Ingest data from various sources with built-in validation to ensure data quality and consistency before analysis.
Handle diverse data types including genomics, proteomics, and phenotypic data to meet the needs of complex bioscience projects.
Drag and drop interface and API integration to facilitate easy data importation processes.
Automatic updates and synchronization of data to provide the latest information for analysis.
The platform allows for over 5000 samples to be ingested weekly for more than 30 customers. This involves harmonizing data and managing ingest processes to facilitate analytics.
The Harmonization Engine reduces processing costs by 4 times compared to industry averages. This optimization helps in managing large datasets efficiently while being cost-effective.
Provides 50+ curation models for metadata annotation. These models help ensure that data is accurately organized and analysis-ready.
Achieves 99% data accuracy which ensures that the harmonized data retains its integrity and reliability for research and analysis.
Effortlessly explore and validate data across transcriptomics, proteomics, metabolomics, and more. This feature allows researchers to move from data to insights faster.
The product integrates multiple biomedical data types and supports advanced analytics. It provides a platform for deriving insights through seamless data processing and visualization.
Users can build custom biomedical cohorts using structured data, ensuring that data is easily accessible and usable for research purposes.
Create precise cohort analyses and customized dashboards with AI assistance, making data management and insights extraction efficient.
Support for conducting comprehensive analysis, visualization, and exploration of data using more than 25 different data modalities, ensuring flexibility and depth in data handling.
Accelerate insight generation using AI tools tailored for biomolecular research, allowing faster and deeper exploration of complex biological data.
Polly operates in a secure virtual private cloud, ensuring an additional layer of data protection.
Controls data access based on user roles, ensuring that only authorized personnel can handle sensitive data.
Employs both in-transit and at-rest encryption with TLS 1.2 protocols and AES-256 encryption for data protection.
Utilizes Amazon RDS for secure database storage, with continuous monitoring and threat detection against SQL injections and brute-force attacks.
Requires additional verification for administrator access, reducing the risk of unauthorized access through compromised credentials.
Offers detailed logging and auditing of resource and user activities within the production environment.
Passwords are securely stored, ensuring conformity to stringent internal protocols.
Ensures fine-grained control over resource access, adhering to the Principle of Least Privilege.
Integrates clinical data, multi-omics data, and biomedical images as part of a unified framework to facilitate R&D efforts.
Makes it seamless to access and analyze longitudinal patient data from integrated sources, supporting research and insights.
Supports complex multi-modal data by incorporating schemas like OMOP while ensuring data integration beyond these models.
Ensures compliance with security protocols such as HIPAA to safeguard data privacy and security in healthcare applications.
Allows for structured and unstructured data ingestion, enabling seamless integration of different data types into one platform.
Involves human expertise in the data harmonization process to ensure accuracy and reliability in handling biomedical data.
Produces high quality data products by integrating and harmonizing various data modalities, allowing for more comprehensive analyses.
Offers customizable dashboards to visualize data and provides AI-driven insights to accelerate research and decision-making processes.
Efficiently processes large-scale omics data with customizable pipelines.
Automates and manages data processing workflows to increase efficiency.
Monitors data processing pipelines to ensure accuracy and speed.
Adds metadata to datasets for better analysis and management.
Structures data for efficient storage and retrieval.
Keeps track of data changes and history for consistency.
Manages storage and access to large datasets.
Integrates data from various API and streaming sources.
Implements AI-driven tools for data analysis and processing.
Provides user-friendly interfaces for data management.
Offers tools for advanced data analysis and scientific research.
Configure and run multiple ETL pipelines tailored to specific data processing needs in biopharma research, ensuring adaptability for different projects and requirements.
Handle large datasets seamlessly with optimizations to prevent bottlenecks and ensure efficient handling and processing of high data volumes.
Automatic monitoring and updating of pipelines to ensure optimal performance without manual intervention, reducing downtime and resource use.
Efficient resource management and optimized pipeline operations lead to significant cost reductions compared to traditional ETL solutions.
Ensures curated metadata attains high accuracy levels by combining AI tools with expert human input. This improves gene ID and cell annotation processes.
Leverages curated data to offer advanced analytics for better insights. Provides tools to process and analyze complex datasets efficiently.
Integrates various metadata types across the organization to ensure consistency and accessibility. Centralizes metadata for streamlined processes.
Supports over 26 different data modalities ensuring robust handling of various data types like single-cell RNA sequencing (scRNA-seq), bulk RNA-seq, etc.
Offers personalized curation of datasets including fields such as age, cell line, cell type, disease, drug, organism, geographical location, sequencing technology, and tissue. This ensures the data is tailored to specific research needs.
Provides customized curation strategies across 25+ data types and 32+ sources, allowing users to handle complex data specific to various indicators and treatments.
Manages large datasets efficiently, ensuring that curation can be performed on a large scale without losing quality or precision.
Ensures datasets are interoperable and scalable for future needs, supporting evolving research requirements like public, in-house, and EDC-curated data.
Use Polly’s APIs to stream data into existing analytical setups, reducing time on formatting and building integrations. It allows users to work with tools of choice.
Host proprietary or open-source applications on Polly’s cloud with production-ready capabilities. Use command line interface and scale applications as needed.
Collaborate with experts to build and customize science-backed applications catered to research needs. Dedicated managers provide support and handle custom requests.
Supports single-cell data types for analysis and machine learning. Allows integration and processing of complex datasets.
Handles bulk RNA sequencing data to facilitate large-scale genomic analyses. Enables integration into the data processing pipeline.
Supports proteomics data to study proteins and their functions. Integrates with existing data models for comprehensive analysis.
Compatible with microarray data analyses, enabling detailed examination of expression patterns and supporting various use-cases.
Create personalized single-cell RNA-seq atlases using your data and publicly available datasets to streamline your research process.
Integrate machine learning solutions to gain deeper insights from your single-cell RNA-seq data, enhancing the precision of your analysis.
Utilize advanced visualization tools to interpret and represent complex single-cell data effectively and communicate your findings clearly.
Access bioinformatics analysis tools specifically designed to handle single-cell RNA-seq data for more structured and in-depth data examination.
Work with curated datasets that ensure the integrity and quality of your single-cell RNA-seq data, providing reliability in research outcomes.
Configures curation processes to fit analysis needs with metadata accuracy and completeness.
Provides solutions for bulk RNA-seq data processing to accelerate discovery workflows.
Utilizes machine learning for enhanced data analysis and insights.
Offers tools for visualizing bulk RNA-seq data for easier interpretation and presentation.
Generates insights from bulk RNA-seq through comprehensive bioinformatics workflows.
Polly delivers Log2 (RMA) transformed microarray datasets, ready for seamless integration with any ML model or normalization method.
Polly automatically cleans, harmonizes, and structures your microarray data, annotating it to fit your custom schema.
Polly’s platform ensures the data is high-quality, checking for integrity, errors, and bias while adhering to scientific compliance standards.
Harmonize microarray data using Polly to integrate and manage datasets efficiently on Polly’s secure cloud.