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Ratings and Reviews 0 Ratings
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What is Illumina Connected Analytics?
Effectively manage, store, and collaborate on multi-omic datasets with ease. The Illumina Connected Analytics platform provides a secure environment for genomic data, enabling the operationalization of informatics and the extraction of valuable scientific insights. Users have the convenience of importing, creating, and modifying workflows using tools like CWL and Nextflow. The platform integrates DRAGEN bioinformatics pipelines, which enhance data processing capabilities. You can securely organize your data within a protected workspace that allows for global sharing while adhering to compliance standards. Retain your data on your own cloud infrastructure while taking advantage of our powerful platform. A versatile analysis environment, including JupyterLab Notebooks, is available for visualizing and interpreting your data effectively. With a scalable data warehouse, you can aggregate, query, and analyze both sample and population data, adapting to your growing needs. By constructing, validating, automating, and deploying informatics pipelines efficiently, you can significantly reduce the time required for genomic data analysis, which is crucial when rapid results are necessary. Additionally, the platform offers extensive profiling capabilities to discover novel drug targets and pinpoint biomarkers for drug response. Lastly, you can seamlessly integrate data from Illumina sequencing systems, ensuring a smooth and efficient workflow experience while optimizing your research outcomes. This comprehensive approach not only enhances productivity but also fosters collaboration among researchers.
What is Genome Analysis Toolkit (GATK)?
Developed by the Data Sciences Platform at the Broad Institute, this all-encompassing toolkit offers a broad spectrum of features that focus largely on variant discovery and genotyping. It boasts a powerful processing engine along with high-performance computing capabilities, making it suitable for handling projects of any size. The GATK is recognized as the gold standard for identifying SNPs and indels in germline DNA as well as RNA sequencing data. Its functionalities are expanding to include detection of somatic short variants, as well as tackling copy number variations (CNV) and structural variations (SV). In addition to the primary variant callers, the GATK features a variety of utilities designed for performing related tasks, such as processing and ensuring the quality of high-throughput sequencing data, and it is complemented by the renowned Picard toolkit. Initially tailored for exome and whole genome data produced by Illumina sequencing technologies, these tools exhibit enough flexibility to adapt to various other sequencing technologies and study designs. As the field of genomics continues to advance, the GATK's versatility guarantees its ongoing relevance in a wide range of genomic research projects, ensuring that it remains a pivotal resource for scientists exploring genetic variations.
Integrations Supported
Docker
Amazon S3
Illumina DRAGEN Secondary Analysis
JupyterLab
Nextflow
API Availability
Has API
API Availability
Pricing Information
Pricing not provided
Free Trial Offered?
Pricing Information
Free
Free Version
Supported Platforms
SaaS
Supported Platforms
SaaS
Windows
Mac
Linux
Customer Service / Support
Standard Support
Web-Based Support
Customer Service / Support
Web-Based Support
Training Options
Documentation Hub
Webinars
Online Training
On-Site Training
Training Options
Documentation Hub
Webinars
Company Facts
Organization Name
Illumina
Company Location
United States
Company Website
www.illumina.com/products/by-type/informatics-products/connected-analytics.html
Company Facts
Organization Name
Broad Institute
Company Location
United States
Company Website
gatk.broadinstitute.org/hc/
Categories and Features
Bioinformatics
Not specified
Genomics Data Analysis
Not specified
Categories and Features
Bioinformatics
Not specified
Genomics Data Analysis
Not specified