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#

cfdna

Here are 26 public repositories matching this topic...

cfDNApipe: A comprehensive quality control and analysis pipeline for cell-free DNA high-throughput sequencing data

  • UpdatedAug 18, 2022
  • Python

Pattern Recognition for Cell-free DNA

  • UpdatedAug 3, 2018
  • Python

R package to work with ctDNA sequencing data

  • UpdatedFeb 20, 2022
  • R

cfDNA cell type of origin estimation

  • UpdatedOct 19, 2023
  • Jupyter Notebook

This is the official development repository for BaseVar, which call variants for large-scale ultra low-pass (<1.0x) WGS data, especially for NIPT data

  • UpdatedMar 6, 2025
  • C

High-intensity sequencing reveals the sources of plasma circulating cell-free DNA variants

  • UpdatedMar 27, 2020
  • R

FinaleToolkit is a package and standalone program to extract fragmentation features of cell-free DNA from paired-end sequencing data.

  • UpdatedMar 12, 2025
  • Python

Important papers relating to the biology of cell free DNA

  • UpdatedSep 21, 2018

R package and vignette to denoise metagenomic cell-free DNA sequencing data.

  • UpdatedNov 5, 2019
  • Roff

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.

  • UpdatedJun 6, 2024
  • Python

LIONHEART is a method for detecting cancer from whole genome sequenced plasma cell-free DNA.

  • UpdatedMar 2, 2025
  • Python

cfDNA methylation probe design from mybaits targeted sequencing

  • UpdatedJul 13, 2018
  • Python

Pipeline to call SNV's with 4 tools (VarDict, LoFreq, Mutect2 & SiNVICT)

  • UpdatedNov 8, 2022
  • Python

This repository serves as a dedicated space for housing the codebase used in our publication for cfGWAS reveal genetic basis of cell-free DNA features. It is intended to provide researchers with access to the methodologies and algorithms employed in our study, facilitating further research and analysis in the field of genetic.

  • UpdatedNov 7, 2024
  • R

Cancer estimation based on nucleosomes: Analysis of proportion of circulating tumor DNA fragments compared to nucleosome references.

  • UpdatedDec 2, 2019
  • C

Alterations in PTEN and ESR1 promote clinical resistance to alpelisib plus aromatase inhibitors

  • UpdatedMar 27, 2020
  • R

Quality Control Workflow for UMI based BAMs

  • UpdatedAug 27, 2024
  • Common Workflow Language

DISMIR: Deep learning-based noninvasive cancer detection by integrating DNA sequence and methylation information of individual cell-free DNA reads

  • UpdatedFeb 12, 2025
  • Python

Plasma cell-free DNA hydroxymethylomes discriminate disease state in EGFR-mutant non-small cell lung cancer.

  • UpdatedMar 17, 2023
  • R

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