Single-molecule, quantitative detection of low-abundance somatic mutations by high-throughput sequencing | Science Advances
Research Sequencing Service: Supported Analysis Pipelines | Research | Dept. of Laboratory Medicine & Pathology | UW Medicine
GitHub - Kennedy-Lab-UW/Duplex-Sequencing
File:Duplex sequencing overview.svg - Wikimedia Commons
IJMS | Free Full-Text | Detection of Low-Frequency Mutations and Identification of Heat-Induced Artifactual Mutations Using Duplex Sequencing
Duplex sequencing - Wikipedia
Duplex sequencing - Wikiwand
Detecting ultralow-frequency mutations by Duplex Sequencing. - Abstract - Europe PMC
What are UMIs and why are they used in high-throughput sequencing? | DNA Technologies Core
Duplex sequencing - Wikipedia
Duplex sequencing - Wikipedia
Detection of ultra-rare mutations by next-generation sequencing | PNAS
Design of single-end duplex-UMI adapter. (a) Schematics showing how... | Download Scientific Diagram
Cool paper #1: duplex-sequencing to detect ultra-rare variants
Oxford Nanopore Tech Update: new Duplex method for Q30 nanopore single molecule reads, PromethION 2, and more
Duplex sequencing - Wikipedia
TwinStrand's Duplex Sequencing Goes Deep: When it comes to detection of low frequency variants, Jesse Salk's technology is one in (ten) million: GEN Edge: Vol 2, No 1
KeyGene Maize B73 Oxford Nanopore duplex sequence data release - KeyGene
Inigo Martincorena on Twitter: "Over 4 years of iterative refinement, Rob Osborne and @AbascalFed identified sources of error in duplex sequencing: end repair, nick extension, mapping errors, DNA contamination… devising solutions to
TwinStrand Duplex Sequencing Technology
Estimating somatic mutation rates by Duplex Sequencing in non-model organisms: Daphnia magna as a case study | bioRxiv
Targeted Single Primer Enrichment Sequencing with Single End Duplex-UMI | Scientific Reports
Development and Application of Duplex Sequencing Strategy for Cell-Free DNA–Based Longitudinal Monitoring of Stage IV Colorectal Cancer - ScienceDirect
