As the volume of genomic data continues to grow, translating it into meaningful scientific insights becomes increasingly challenging, demanding substantial computational power and advanced bioinformatics techniques. This is further complicated when data resides across different laboratories and biobanks, creating bottlenecks and delaying research progress. Our upcoming webinar explores how Seqera is lowering the barrier to bioinformatics tools, making it easier than ever to perform end-to-end scientific data analysis all in one place:
About
Join Esha Joshi (Scientific Engagement Lead) and Rob Syme (Scientific Support Lead) as they showcase how Seqera is bridging the gap between the wet lab experimentation and computational analyses.
- Discover the right data pipeline: Use Seqera AI, the bioinformatics agent built for the R&D lifecycle, to find the most suitable data pipeline for your genomics analysis, with clear, comprehensive explanations.
- Locate pipelines with ease: Quickly locate your chosen data pipeline with one-click using Seqera Pipelines, an open-source repository of pipelines from organizations including Sanger and QBIC.
- Centralize your data analysis: Keep your experimental data organized, monitor sample processing from submission to results (with clear status updates and QC metrics) and perform interactive analyses.
- Collaborate in real-time: Easily collaborate with bioinformatics teams and colleagues by sharing your data and validating results in a secure environment, enabling faster validation and feedback.
Form not loading? Check your browser security settings, or try a different browser. If the problem persists, please contact marketing@seqera.io.
Speakers
Esha Joshi
Scientific Engagement Lead at Seqera
Rob Syme
Scientific Support Lead at Seqera