Automation for KAPA® HyperPlus™ Kits
Automation for KAPA® HyperPlus™ Kits | The Sciclone® G3 NGSx iQ™ workstation (Figure 1) is specifically designed to automate the most complex Next Generation Sequencing (NGS) library construction workflows.
Automate your Twist® Human Core Exome Kit on the Sciclone® G3 NGSx Workstation!
Exome Sequencing using Rapid Automation Technology | Efficient library construction for Next Generation Sequencing (NGS) of human whole exome sequencing (WES) is fundamentally improved with the superior oligo prob design and performance of the Twist® Human Core Exome Kit. This kit enables increased uniformity and enables increased uniformity and deeper coverage of difficult regions while driving down the cost per sample.
Preventing Cross Contamination with Automated Walk-Away Library Prep
Contamination-Free, Worry-Free, Walk-Away Library Prep Automation | Automation of library preparation increases throughput, reduces labor costs, and eliminates many of the sources of human error. As most next generation sequencing (NGS) library preparation protocols include one or more polymerase chain reaction (PCR) steps, an on-deck thermal cycler is needed to achieve true walk-away automation.
Perspectives on Small RNA Sequencing
Challenges and Complications of Small RNA Library Prep | This webinar will address a range of methods for optimizing small RNA library preparation. Anitha Jayaprakash, co-founder of T-cell receptor sequencing firm Girihlet, will provide her perspectives on sequencing small RNAs and its utility in the study of various applications...
Soil Metagenomics
Comprehensive Workflow for Soil Metagenomics Analysis Using Shotgun Sequencing | This webinar will discuss a comprehensive end-to-end workflow for soil metagenomic shotgun sequencing that offers an unbiased alternative to amplicon-based approaches to assess the composition of culture-free microbial communities and predict functional profiles...
Engineering Better Cannabis
Using CRISPR as a Tool to Develop Designer Cannabis | CRISPR Cas9 is an efficient and reliable genome editing technology which allows researchers to make precise, targeted changes to the genome of living cells by removing, adding or altering sections of an organism’s DNA sequence...
Aneuploid Findings with Independent NGS Platforms
Comparing the Reproducibility of Different Aneuploid Findings | This webinar describes a study that used two independent next-generation sequencing (NGS) platforms to gain insight into the impact of different types of aneuploidies during preimplantation genetic testing....
When to Size Select
Fragmentation Method Effects on Size Selection Needs | Fragmentation of nucleic acids prior to library construction is required by the majority of next-generation sequencing platforms. Available methods for fragmenting high quality genomic DNA vary in their ability to focus sheared nucleic acids to a tight average fragment size. Broadly distributed shearing profiles are obtained when using probe-based...