Webinar: Whole genome & exome sequencing from low input samples using Swift Biosciences’ 2S Technology

Swift's 2S Technology yields high complexity NGS libraries and improves sample coverage, thereby revealing even difficult to read sequences in your NGS samples. Attend our webinar and learn how to harness the 2S Technology for improving coverage in your NGS experiments.

The Accel-NGS 2S Hyb DNA Library Kit, designed for Illumina^® platforms, produces fewer duplicates at 1 ng to save you money on sequencing costs. A variety of indexing kits allow for compatibility with multiple hybridization capture technologies: Swift Hybridization Capture Kits, IDT^® xGen^®Lockdown^® Probes, Twist Human Core Exome Kit and Agilent SureSelect. This kit is the right choice for researchers working with applications pertaining to low input FFPE DNA or whole genome sequencing of liquid biopsy and cfDNA samples.

Benefits

Compatibility with limiting FFPE and cfDNA samples
More unique molecules available for capture
Meaningful data from low input samples
Suitable for a diverse set of panels
Readily automatable
Increase confidence of low-frequency variant calling and improve data retention

Learn all about Swift's 2S Technology by attending the webinar organized by Swift, BioCat and LubioScience:

Friday 23 October 2020, 11:00-11:45 (CEST)