A simplified pipeline for ctDNA sequencing data analysis
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Updated
Sep 23, 2017 - Shell
A simplified pipeline for ctDNA sequencing data analysis
R package to work with ctDNA sequencing data
High-intensity sequencing reveals the sources of plasma circulating cell-free DNA variants
Deduplication for cfDNA sequencing data
Python package for cancer early detection based on a model of cancer evolution and circulating tumor DNA (ctDNA) shedding
Pipeline to call SNV's with 4 tools (VarDict, LoFreq, Mutect2 & SiNVICT)
As a tool for cancer subtype prediction, Keraon uses features derived from cell-free DNA (cfDNA) in conjunction with PDX reference models to perform both classification and heterogenous phenotype fraction estimation.
Cancer estimation based on nucleosomes: Analysis of proportion of circulating tumor DNA fragments compared to nucleosome references.
Supplementary files for Paracchini, Beltrame et al., Clin Cancer Res, 2020.
Structural Variants in cell-free tumor DNA
Workflow for collapsing of standard binary alignment mapping file generated by MSK-ACCESS
Diagnostic performance of HPV-DeepSeek, a hybrid capture whole genome sequencing liquid biopsy for HPV-associated cancers
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