Automating High-Throughput Sample Prep for Analysis of Complex Diseases Using Next-Gen Sequencing
Increasing NGS Sequencing Capacity with High-Throughput Automated TruSeq Stranded mRNA Library Construction
This educational webinar includes an overview of the transcriptome, Illumina's RNASeq Stranded Library Kits and automation considerations and insights for generating sequence-ready libraries and quality results.
First in a three-part series on automation for smaller labs and those less familiar with automation who are interested in automation to standardize workflows and improve results. This webinar provides an introduction to automating NGS workflows including library preparation methods overview and automation considerations.
Michaela Bowden (CEMOP Associate Director, Dana Farber Cancer Institute) presents the utility of Biomek automation (library prep, etc.) and using biopsied/low RNA-input (FFPE) samples for clinically relevant results. Includes overview of the RNA-Seq workflow and Illumina's Script-Seq Complete, TruSeq Stranded mRNA kits.
This educational webinar offers an overview of FFPE samples—opportunities and challenges with this sample type, DNA extraction from FFPE for genomics sequencing and impacts to downstream applications such as NGS, FFPE extraction kit overview and automated method.
Part 2 in three-part series covering automated NGS workflows. This session addresses automated DNA & RNA sequencing methods including whole genome sequencing and Illumina products (TrueSeq DNA PCR-Free, Nano DNA); targeted DNA sequencing including Agilent HaloPlex; the transcriptome and automated total RNA and mRNA sequencing and library construction/QC, including a results overview.