Next-generation sequencing applications enable researchers to delve deeper into the human genome. Although NGS applications allow diverse and detailed analysis, NGS library preparation is encumbered by extensive hands-on and labor-intensive workflows. To address this, the Apollo system provides a complete, walkaway solution using validated protocols and chemistries that produce consistent libraries for DNA-seq, RNA-seq, and ChIP-seq applications.
Simplify NGS library prep with a flexible, streamlined workflow
The Apollo system offers best-in-class performance and flexibility. Manual NGS library prep workflows are labor-intensive and prevent you from conducting other valuable experiments. The Apollo system frees you from manual steps by automating the critical portions of the workflow, reducing your hands-on time to just 30 minutes, depending on the sample throughput and script used.
The Apollo system can also run flexible batch sizes without wasting reagents or time. In addition to both DNA and RNA NGS library prep protocols, this versatile system efficiently performs related protocols for sample preparation and cleanup, such as poly A+ RNA enrichment, rRNA depletion, and PCR cleanup.
Maximize yield and consistency with automated processing and validated protocols
Manual NGS library preparation is not only time-consuming, but it is also subject to human error, affecting the quality of your data. Consistency is key when processing multiple samples; the Apollo system, combined with PrepX chemistries and scripts, allows you to create consistent target libraries without the variability caused by manual pipetting.