cfTools: an R/Bioconductor package for deconvolving cell-free DNA via methylation analysis

Cell-free DNA (cfDNA) released by dying cells from damaged or diseased tissues can lead to elevated tissue-specific DNA, which is traceable and quantifiable through unique DNA methylation patterns. Therefore, tracing cfDNA origins by analyzing its methylation profiles holds great potential for detec...

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Published inBioinformatics advances Vol. 5; no. 1; p. vbaf108
Main Authors Hu, Ran, Li, Shuo, Stackpole, Mary L, Li, Qingjiao, Zhou, Xianghong Jasmine, Li, Wenyuan
Format Journal Article
LanguageEnglish
Published England 01.01.2025
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ISSN2635-0041
2635-0041
DOI10.1093/bioadv/vbaf108

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Abstract Cell-free DNA (cfDNA) released by dying cells from damaged or diseased tissues can lead to elevated tissue-specific DNA, which is traceable and quantifiable through unique DNA methylation patterns. Therefore, tracing cfDNA origins by analyzing its methylation profiles holds great potential for detecting and monitoring a range of diseases, including cancers. However, deconvolving tissue-specific cfDNA remains challenging for broader applications and research due to the scarcity of specialized, user-friendly bioinformatics tools. To address this, we developed cfTools, an R package that streamlines cfDNA tissue-of-origin analysis for disease detection and monitoring. Integrating advanced cfDNA tissue deconvolution algorithms with R/Bioconductor compatibility, cfTools offers data preparation and analysis functions with flexible parameters for user-friendliness. By identifying abnormal cfDNA compositions, cfTools can infer the presence of underlying pathological conditions, including but not limited to cancer. It simplifies bioinformatics tasks and enables users without advanced expertise to easily derive biologically interpretable insights from standard preprocessed sequencing data, thus increasing its accessibility and broadening its application in cfDNA-based disease studies. cfTools and its supplementary package cfToolsData are freely available at Bioconductor: https://bioconductor.org/packages/release/bioc/html/cfTools.html and https://bioconductor.org/packages/release/data/experiment/html/cfToolsData.html. The development version of cfTools is maintained on GitHub: https://github.com/jasminezhoulab/cfTools.
AbstractList Cell-free DNA (cfDNA) released by dying cells from damaged or diseased tissues can lead to elevated tissue-specific DNA, which is traceable and quantifiable through unique DNA methylation patterns. Therefore, tracing cfDNA origins by analyzing its methylation profiles holds great potential for detecting and monitoring a range of diseases, including cancers. However, deconvolving tissue-specific cfDNA remains challenging for broader applications and research due to the scarcity of specialized, user-friendly bioinformatics tools.MotivationCell-free DNA (cfDNA) released by dying cells from damaged or diseased tissues can lead to elevated tissue-specific DNA, which is traceable and quantifiable through unique DNA methylation patterns. Therefore, tracing cfDNA origins by analyzing its methylation profiles holds great potential for detecting and monitoring a range of diseases, including cancers. However, deconvolving tissue-specific cfDNA remains challenging for broader applications and research due to the scarcity of specialized, user-friendly bioinformatics tools.To address this, we developed cfTools, an R package that streamlines cfDNA tissue-of-origin analysis for disease detection and monitoring. Integrating advanced cfDNA tissue deconvolution algorithms with R/Bioconductor compatibility, cfTools offers data preparation and analysis functions with flexible parameters for user-friendliness. By identifying abnormal cfDNA compositions, cfTools can infer the presence of underlying pathological conditions, including but not limited to cancer. It simplifies bioinformatics tasks and enables users without advanced expertise to easily derive biologically interpretable insights from standard preprocessed sequencing data, thus increasing its accessibility and broadening its application in cfDNA-based disease studies.ResultsTo address this, we developed cfTools, an R package that streamlines cfDNA tissue-of-origin analysis for disease detection and monitoring. Integrating advanced cfDNA tissue deconvolution algorithms with R/Bioconductor compatibility, cfTools offers data preparation and analysis functions with flexible parameters for user-friendliness. By identifying abnormal cfDNA compositions, cfTools can infer the presence of underlying pathological conditions, including but not limited to cancer. It simplifies bioinformatics tasks and enables users without advanced expertise to easily derive biologically interpretable insights from standard preprocessed sequencing data, thus increasing its accessibility and broadening its application in cfDNA-based disease studies.cfTools and its supplementary package cfToolsData are freely available at Bioconductor: https://bioconductor.org/packages/release/bioc/html/cfTools.html and https://bioconductor.org/packages/release/data/experiment/html/cfToolsData.html. The development version of cfTools is maintained on GitHub: https://github.com/jasminezhoulab/cfTools.Availability and implementationcfTools and its supplementary package cfToolsData are freely available at Bioconductor: https://bioconductor.org/packages/release/bioc/html/cfTools.html and https://bioconductor.org/packages/release/data/experiment/html/cfToolsData.html. The development version of cfTools is maintained on GitHub: https://github.com/jasminezhoulab/cfTools.
Cell-free DNA (cfDNA) released by dying cells from damaged or diseased tissues can lead to elevated tissue-specific DNA, which is traceable and quantifiable through unique DNA methylation patterns. Therefore, tracing cfDNA origins by analyzing its methylation profiles holds great potential for detecting and monitoring a range of diseases, including cancers. However, deconvolving tissue-specific cfDNA remains challenging for broader applications and research due to the scarcity of specialized, user-friendly bioinformatics tools. To address this, we developed cfTools, an R package that streamlines cfDNA tissue-of-origin analysis for disease detection and monitoring. Integrating advanced cfDNA tissue deconvolution algorithms with R/Bioconductor compatibility, cfTools offers data preparation and analysis functions with flexible parameters for user-friendliness. By identifying abnormal cfDNA compositions, cfTools can infer the presence of underlying pathological conditions, including but not limited to cancer. It simplifies bioinformatics tasks and enables users without advanced expertise to easily derive biologically interpretable insights from standard preprocessed sequencing data, thus increasing its accessibility and broadening its application in cfDNA-based disease studies. cfTools and its supplementary package cfToolsData are freely available at Bioconductor: https://bioconductor.org/packages/release/bioc/html/cfTools.html and https://bioconductor.org/packages/release/data/experiment/html/cfToolsData.html. The development version of cfTools is maintained on GitHub: https://github.com/jasminezhoulab/cfTools.
Author Li, Qingjiao
Stackpole, Mary L
Li, Wenyuan
Hu, Ran
Zhou, Xianghong Jasmine
Li, Shuo
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Cites_doi 10.1093/bioinformatics/btr167
10.1186/s13059-024-03275-x
10.3389/fgene.2021.671057
10.1038/s41467-021-22901-x
10.1038/nrc.2017.7
10.1093/nargab/lqad048
10.1038/s41586-022-05580-6
10.1080/15592294.2020.1816774
10.1038/s41467-018-07466-6
10.1093/nar/gky423
10.1038/npp.2012.112
10.1093/bib/bby029
10.3390/cancers11111741
10.3389/fimmu.2023.1148722
10.1073/pnas.2305236120
10.1016/j.annonc.2020.02.011
10.1038/s41467-022-32995-6
10.1073/pnas.1508736112
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References Del Vecchio (2025061901551611300_vbaf108-B3) 2021; 16
Moore (2025061901551611300_vbaf108-B13) 2013; 38
Stackpole (2025061901551611300_vbaf108-B15) 2022; 13
Huang (2025061901551611300_vbaf108-B5) 2019; 11
Manel (2025061901551611300_vbaf108-B12) 2008
Zhang (2025061901551611300_vbaf108-B19) 2023; 14
Caggiano (2025061901551611300_vbaf108-B2) 2021; 12
Li (2025061901551611300_vbaf108-B9) 2018; 46
Feng (2025061901551611300_vbaf108-B4) 2019; 20
Li (2025061901551611300_vbaf108-B8) 2023; 120
Sun (2025061901551611300_vbaf108-B16) 2015; 112
Moss (2025061901551611300_vbaf108-B14) 2018; 9
Wan (2025061901551611300_vbaf108-B18) 2017; 17
Keukeleire (2025061901551611300_vbaf108-B6) 2023; 5
Krueger (2025061901551611300_vbaf108-B7) 2011; 27
Loyfer (2025061901551611300_vbaf108-B11) 2023; 613
Liu (2025061901551611300_vbaf108-B10) 2020; 31
Barefoot (2025061901551611300_vbaf108-B1) 2021; 12
Unterman (2025061901551611300_vbaf108-B17) 2024; 25
References_xml – start-page: 1148
  volume-title: N Engl J Med
  year: 2008
  ident: 2025061901551611300_vbaf108-B12
– volume: 27
  start-page: 1571
  year: 2011
  ident: 2025061901551611300_vbaf108-B7
  article-title: Bismark: a flexible aligner and methylation caller for Bisulfite-Seq applications
  publication-title: Bioinformatics
  doi: 10.1093/bioinformatics/btr167
– volume: 25
  start-page: 151
  year: 2024
  ident: 2025061901551611300_vbaf108-B17
  article-title: CelFiE-ISH: a probabilistic model for multi-cell type deconvolution from single-molecule DNA methylation haplotypes
  publication-title: Genome Biol
  doi: 10.1186/s13059-024-03275-x
– volume: 12
  start-page: 671057
  year: 2021
  ident: 2025061901551611300_vbaf108-B1
  article-title: Detection of cell types contributing to cancer from circulating, cell-free methylated DNA
  publication-title: Front Genet
  doi: 10.3389/fgene.2021.671057
– volume: 12
  start-page: 2717
  year: 2021
  ident: 2025061901551611300_vbaf108-B2
  article-title: Comprehensive cell type decomposition of circulating cell-free DNA with CelFiE
  publication-title: Nat Commun
  doi: 10.1038/s41467-021-22901-x
– volume: 17
  start-page: 223
  year: 2017
  ident: 2025061901551611300_vbaf108-B18
  article-title: Liquid biopsies come of age: towards implementation of circulating tumour DNA
  publication-title: Nat Rev Cancer
  doi: 10.1038/nrc.2017.7
– volume: 5
  start-page: lqad048
  year: 2023
  ident: 2025061901551611300_vbaf108-B6
  article-title: Cell type deconvolution of methylated cell-free DNA at the resolution of individual reads
  publication-title: NAR Genom Bioinform
  doi: 10.1093/nargab/lqad048
– volume: 613
  start-page: 355
  year: 2023
  ident: 2025061901551611300_vbaf108-B11
  article-title: A DNA methylation atlas of normal human cell types
  publication-title: Nature
  doi: 10.1038/s41586-022-05580-6
– volume: 16
  start-page: 642
  year: 2021
  ident: 2025061901551611300_vbaf108-B3
  article-title: Cell-free DNA methylation and transcriptomic signature prediction of pregnancies with adverse outcomes
  publication-title: Epigenetics
  doi: 10.1080/15592294.2020.1816774
– volume: 9
  start-page: 5068
  year: 2018
  ident: 2025061901551611300_vbaf108-B14
  article-title: Comprehensive human cell-type methylation atlas reveals origins of circulating cell-free DNA in health and disease
  publication-title: Nat Commun
  doi: 10.1038/s41467-018-07466-6
– volume: 46
  start-page: e89–e89
  year: 2018
  ident: 2025061901551611300_vbaf108-B9
  article-title: CancerDetector: ultrasensitive and non-invasive cancer detection at the resolution of individual reads using cell-free DNA methylation sequencing data
  publication-title: Nucleic Acids Res
  doi: 10.1093/nar/gky423
– volume: 38
  start-page: 23
  year: 2013
  ident: 2025061901551611300_vbaf108-B13
  article-title: DNA methylation and its basic function
  publication-title: Neuropsychopharmacology
  doi: 10.1038/npp.2012.112
– volume: 20
  start-page: 585
  year: 2019
  ident: 2025061901551611300_vbaf108-B4
  article-title: Disease prediction by cell-free DNA methylation
  publication-title: Brief Bioinform
  doi: 10.1093/bib/bby029
– volume: 11
  start-page: 1741
  year: 2019
  ident: 2025061901551611300_vbaf108-B5
  article-title: Cell-free DNA methylation profiling analysis—technologies and bioinformatics
  publication-title: Cancers (Basel)
  doi: 10.3390/cancers11111741
– volume: 14
  start-page: 1148722
  year: 2023
  ident: 2025061901551611300_vbaf108-B19
  article-title: Insights into the role of nucleotide methylation in metabolic-associated fatty liver disease
  publication-title: Front Immunol
  doi: 10.3389/fimmu.2023.1148722
– volume: 120
  start-page: e2305236120
  year: 2023
  ident: 2025061901551611300_vbaf108-B8
  article-title: Comprehensive tissue deconvolution of cell-free DNA by deep learning for disease diagnosis and monitoring
  publication-title: Proc Natl Acad Sci U S A
  doi: 10.1073/pnas.2305236120
– volume: 31
  start-page: 745
  year: 2020
  ident: 2025061901551611300_vbaf108-B10
  article-title: Sensitive and specific multi-cancer detection and localization using methylation signatures in cell-free DNA
  publication-title: Annals of Oncology
  doi: 10.1016/j.annonc.2020.02.011
– volume: 13
  start-page: 5566
  year: 2022
  ident: 2025061901551611300_vbaf108-B15
  article-title: Cost-effective methylome sequencing of cell-free DNA for accurately detecting and locating cancer
  publication-title: Nat Commun
  doi: 10.1038/s41467-022-32995-6
– volume: 112
  year: 2015
  ident: 2025061901551611300_vbaf108-B16
  article-title: Plasma DNA tissue mapping by genome-wide methylation sequencing for noninvasive prenatal, cancer, and transplantation assessments
  publication-title: Proc Natl Acad Sci USA
  doi: 10.1073/pnas.1508736112
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