A study design tool that combines private data with public data sets for rapidly building and exploring cohorts.
Integrated into Illumina Connected Analytics, Illumina Connected Analytics Cohorts combines multiomic and phenotypic data in a single place to allow for greater analysis of cohorts and increase novel research insights. Illumina Connected Analytics Cohorts delivers:
Leverage data models for combining genomic and phenotypic data and access professional services for custom loading and harmonization.
Use the browser to find the right subjects for your cohort and integrate genomic and phenotypic data to review summary statistics.
Easily access workflows, including DRAGEN pipelines, and export to Illumina Connected Analytics Bench for enhanced data science studies.
| Instruments | MiSeq System, iSeq 100 System, NextSeq 550 System, NextSeq 2000 System, NextSeq 1000 System, MiSeqDx in Research Mode, MiniSeq System, NovaSeq X System, NovaSeq 6000Dx in Research Mode, NextSeq 500 System, iScan System, NovaSeq 6000 System, NovaSeq X Plus System |
|---|---|
| Software format | Cloud |
| Technology | Sequencing |
HIPAA Compliant Attested by Schellman
Illumina Connected Analytics features an information security program that leverages the Amazon Web Services infrastructure and provides multiple layers of security. Its risk management program conforms to the specifications of the Health Insurance Portability and Accountability Act (HIPAA) Security Role and the Health Information Technology for Economic and Clinical Health (HITECH) Breach Notification Rule.
ISO 27001 Certified by Schellman
Illumina has received ISO 27001 certification of its information security management system (ISMS) supporting Illumina Connected Analytics. This certification ensures that sensitive data contained or collected by these solutions are protected. The certification was performed by Schellman, an ANSI National Accreditation Board (ANAB) and United Kingdom Accreditation Service (UKAS) accredited certification body based in the US.
ISO 27701 Certified by Schellman
Illumina Connected Analytics is compliant with global and local data privacy and requirements with 27701:2019 certification and guaranteed data residency.
ISO 13485 Certified by BSI
llumina Connected Analytics (ICA) was developed in accordance with Illumina’s Software Life Cycle (SLC) process under Illumina’s Quality Management System.
Illumina operates and maintains a Quality Management System (QMS) which complies with the requirements of ISO 13485. The scope of the QMS covers the Design, Development, Manufacture, Distribution, Installation and Servicing of Genotyping, Gene Expression and PCR – products instruments and software - used for genetic analysis. Additionally, processes within Illumina’s QMS have adopted industry best practices and relevant standards, such as ISO 14971 for Risk Management and IE62304 for SLC.
GDPR
Illumina Connected Analytics features multiple system controls that you can use to manage authorization, authentication, and data control, including deletion as needed. Access logs are retained for seven years. These features help researchers ensure compliance with the General Data Protection Regulation (GDPR).
An Illumina Connected Analytics license is required. There are no additional costs in iCredits, storage, or consumption for ICA Cohorts.
Illumina Connected Analytics Cohorts combines subject- and sample-level metadata with molecular data to perform tertiary analyses on selected subsets of individuals for a wide variety of applications, including drug discovery, cancer research, and more.
Efficient sample tracking and workflow management for genomics labs.
Streamlined cloud-based run setup and monitoring.
A secure, scalable bioinformatics platform for seamless sequencer integration and flexible workflows.
Accurate, comprehensive, and efficient analysis of NGS data.
Accurate, comprehensive and efficient secondary analysis for Infinium microarray-based assays.
BaseSpace Sequence Hub offers a wide variety of NGS data analysis apps for common Illumina sequencing methods.
Emedgene streamlines tertiary analysis workflows for rare disease genomics and other germline research applications.
An interactive omics knowledge base that analyzes private omics data with highly curated public data to help researchers put their data into biological context.
Use multiomics profiling to multiply discovery power and better connect genotype to phenotype.
Our variant annotation and analysis software tools can help researchers extract and report biological insights from large volumes of genomic data.
Illumina provides an innovative portfolio of NGS systems, products, and services for many phases of the drug development pipeline.
Using whole-genome sequencing to study early-onset Parkinson’s Disease
NysnoBio is developing a gene therapy to slow progression of Parkinson's disease in people under age 50.
Illumina Connected Analytics Cohorts: Multiomic cancer workflow demo
Learn how Illumina Connected Analytics Cohorts helps researchers build a case and control oncology cohort definition out of complex datasets.
An Illumina Connected Analytics license is required. There is no additional cost in iCredits, storage, or consumption for Illumina Connected Analytics Cohorts.
Learn more about:
* 250 iCredits expire after 30-day introductory trial.
** Available for systems with control software that support Universal Copy Service. Not available for all legacy systems.
Illumina Connected Analytics Cohorts provides a friendly user interface for filtering and visualizing genomic and phenotypic data of cohorts. Easily evaluate data comparisons for feasibility analysis on select cohort definition.
Connecting multiomics data with informatics
In this webinar, you’ll hear bioinformatics experts discuss multiomics data set integration challenges, tools to overcome these challenges, and informatics hurdles yet to be resolved.
Using analytics to improve cancer research
Learn how the Genomics Platform Group uses Illumina Connected Analytics to transform sequencing workflows by optimizing analytics pipelines and collaborating in a secure, compliant data environment.
ICA Cohorts
20065842
Illumina Connected Analytics (ICA) Cohorts empowers scientists to analyze aggregated genomic data to understand genotype-phenotype relationships, identify potential disease drivers, and discover new biomarkers.
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If a study has been loaded into the Illumina Connected Analytics Cohorts, customer administrators can select permission to share the study with collaborators.
Yes. Private data can be imported into the Illumina Connected Analytics Cohorts and analyzed independently or combined with public data to expand cohort analysis.
Illumina Connected Analytics Cohorts supports genomic data from DNA sequencing (eg, single nucleotide changes, CNV, germline, and somatic calls) and RNA-Seq (eg, TPM and differential expression) studies, phenotypic data of medical attributes (eg, demographics, medical history, and therapeutic interventions), and over 27,000 subject-level data sets across public databases (eg, TCGA, Broad RGP, DRAGEN 1kGP, and GEO).
Advanced chemistry, optics, and informatics combine to deliver exceptional speed and data quality, outstanding throughput and scalability.
Optimized reagent kit that provides increased cluster density and read length, improving sequencing quality scores compared to earlier versions.
Enable CGP with a large pan-cancer panel covering all major variant classes plus gene signatures (TMB, MSI, and HRD) from FFPE tissue.
A fast, integrated workflow for preparing libraries for use in a wide range of sequencing applications.
Operationalize informatics and drive scientific insights with Illumina Connected Analytics. Contact us for information on pricing, subscriptions, and more.
Maximize genomic insights with DRAGEN secondary analysis, learn about the latest updates, read FAQs, and find product support.
An interactive omics knowledge base that analyzes private omics data with highly curated public data to help researchers put their data into biological context.
* 250 iCredits expire after 30-day introductory trial.
** Available for systems with control software that support Universal Copy Service. Not available for all legacy systems.
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