Files

2017-Leveraging Molecular IDs to Improve Coverage of Low Frequency Variants in Ovarian Cancer Using Next Generation Sequencing.pdf
2018-A Universal Analysis Pipeline for Hybrid Capture-Based Targeted Sequencing Data with Unique Molecular Indexes.pdf
2018-Unique, dual-indexed sequencing adapters with UMIs effectively eliminate index cross- talk and significantly improve sensitivity of massively parallel sequencing.pdf
2019-High efficiency error suppression for accurate detection of low-frequency variants.pdf
2019-Performance evaluation of commercial library construction kits for PCR-based targeted sequencing using a unique molecular identifier.pdf
Breaking the NGS Noise Barrier to Accurately Detect Variants below 1% Allele Frequency.pdf
README.md
Technical-Note.pdf
idt_analysisguideline_varcall-umis-dupseqadapters.pdf
pre_UMI.py

2018-Unique, dual-indexed sequencing adapters with UMIs effectively eliminate index cross- talk and significantly improve sensitivity of massively parallel sequencing.pdf

Oct 24, 2019

d733f75 · Oct 24, 2019