Improve NGS Data Quality & Usability
The Platform for Science adapts to the way you work, collecting data along the way. Capture and track Next-Generation Sequencing (NGS) data easily and accurately from lineage and accessioning, to sequencing, and beyond. Meet your scientific objectives by using NGS data in context – associations are created between samples, containers, projects, and other relevant entities to ensure accurate processing and reporting of each sample.
Keep Pace with Advancements in Technology
The Platform for Science is built to work with instruments and consumables from the vendors you choose. Whether you use Next-Generation Sequencing, Microarray, Sanger, or other techniques, you can add new workflows and new hardware without losing any of your data or current processes in your lab. Long reads, short reads, and SNPs, from high-throughput down to base pairs, the Platform for Science lets you work your way when analyzing and tracking your data.
Enable Research & Clinical Workflows
NGS solutions from Core Informatics are designed to support research and clinical workflows. Collect the information needed to obtain or maintain clinically regulated certifications such as CAP/CLIA and comply with HIPAA and HITECH regulations. Choose to deploy both types of workflows in parallel, or leverage the multitenant capabilities of Core’s Platform for Science to separate your business groups.
Click to view a webinar hosted by Mount Sinai.
Lab Informatics Solutions to Meet NGS Lab Needs.
NGS is a cross-cutting technology, its impact extends across industries. Core Informatics’ customers use our NGS solutions to facilitate research for population wide association studies, study how the gut microbiome contributes to Crohn’s and bowel syndromes, profile tumor samples to better recommend courses of treatment, and more. The diversity of uses illustrates the flexibility of the Platform for Science to respond to new science and emerging needs.
Click here to learn how Core’s genomics solutions can help to manage your data and optimize processes.
Additional Integrations Available for Next-Generation Sequencing Lab Systems
With the Platform for Science Marketplace, you can choose from easily configurable apps matching your NGS workflow. Pre-configured apps are available for your library prep kits and sequencers. Connect to industry-standard quality control systems. Then integrate with leading analysis systems to rapidly convert raw data into the results that drive genomics projects.
Manage and track all aspects of sequencing on Illumina HiSeq®, MiSeq®, MiniSeq®, and NextSeq®; Ion PGM™, and Proton™ systems.
Access templates for whole genome, exome, amplicon, and RNA sequencing including an extensive array of Illumina TruSeq® Sample and Library Prep kits, Agilent SureSelect XT and XT2 Exome Library Prep, KAPA® Library Prep, Ion AmpliSeq™, and TargetSeq™, Exome Library Prep kits and more.
Capture analytical results from industry standard instruments including the Thermo Fisher Qubit®, Agilent TapeStation®, PerkinElmer LabChip® GX, Nanodrop, MD SpectraMax® and more.
Support automated processes with liquid handler robotic instrumentation including the PerkinElmer Sciclone®, Agilent Bravo™, Beckman Coulter Biomek® FX, Tecan Freedom Evo®, Hamilton Star™ and more.
Integrate with leading bioinformatics pipelining, and secondary and tertiary analysis platforms.
Capture and track genomic data from sample accessioning to final report generation, helping to optimize outcomes.
Biologics Discovery Solution
Accelerate execution of end-to-end biologics workflows and easily add new modalities, lineage requirements, and processes over time.