4.6 Review

Bridging biological cfDNA features and machine learning approaches

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Profiling of circulating tumor DNA and tumor tissue for treatment selection in patients with advanced and refractory carcinoma: a prospective, two-stage phase II Individualized Cancer Treatment trial

Jakob M. Riedl et al.

Summary: The study evaluated the success of a targeted therapy selected by profiling of ctDNA and tissue in patients with advanced and refractory carcinoma. The results indicate that more innovative approaches to study design and matching algorithms are necessary to achieve improved patient outcomes.

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Detection and characterization of jagged ends of double-stranded DNA in plasma

Peiyong Jiang et al.

GENOME RESEARCH (2020)

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Rossa W. K. Chiu et al.

CLINICAL CHEMISTRY (2020)

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A mathematical model of ctDNA shedding predicts tumor detection size

Stefano Avanzini et al.

SCIENCE ADVANCES (2020)

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Finding new cancer epigenetic and genetic biomarkers from cell-free DNA by combining SALP-seq and machine learning

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David W. Cescon et al.

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Long fragments achieve lower base quality in Illumina paired-end sequencing

Ge Tan et al.

SCIENTIFIC REPORTS (2019)

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Genome-wide cell-free DNA fragmentation in patients with cancer

Stephen Cristiano et al.

NATURE (2019)

Editorial Material Oncology

Circulating Tumor DNA as a Marker for Disease Relapse in Early-Stage Breast Cancer-Bad Blood

Swathi Karthikeyan et al.

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Isaac Garcia-Murillas et al.

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Early Cancer Detection from Multianalyte Blood Test Results

Ka-Chun Wong et al.

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False-Positive Plasma Genotyping Due to Clonal Hematopoiesis

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CLINICAL CANCER RESEARCH (2018)

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Evaluation of pre-analytical factors affecting plasma DNA analysis

Havel Markus et al.

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Florent Mouliere et al.

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Review Medicine, General & Internal

Application of Cell-free DNA Analysis to Cancer Treatment

Ryan B. Corcoran et al.

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Preferred end coordinates and somatic variants as signatures of circulating tumor DNA associated with hepatocellular carcinoma

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Enhanced detection of circulating tumor DNA by fragment size analysis

Florent Mouliere et al.

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Review Medicine, Research & Experimental

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Sonia Khier et al.

FUTURE SCIENCE OA (2018)

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Comparative analysis of 12 different kits for bisulfite conversion of circulating cell-free DNA

Mai-Britt Worm Orntoft et al.

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UMI-tools: modeling sequencing errors in Unique Molecular Identifiers to improve quantification accuracy

Tom Smith et al.

GENOME RESEARCH (2017)

Article Multidisciplinary Sciences

Phylogenetic ctDNA analysis depicts early-stage lung cancer evolution

Christopher Abbosh et al.

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Integrating liquid biopsies into the management of cancer

Giulia Siravegna et al.

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Direct detection of early-stage cancers using circulating tumor DNA

Jillian Phallen et al.

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Single-Stranded DNA Library Preparation Does Not Preferentially Enrich Circulating Tumor DNA

Tina Moser et al.

CLINICAL CHEMISTRY (2017)

Article Medical Laboratory Technology

DNA of Erythroid Origin Is Present in Human Plasma and Informs the Types of Anemia

W. K. Jacky Lam et al.

CLINICAL CHEMISTRY (2017)

Review Oncology

Liquid biopsies come of age: towards implementation of circulating tumour DNA

Jonathan C. M. Wan et al.

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A comparison of reference-based algorithms for correcting cell-type heterogeneity in Epigenome-Wide Association Studies

Andrew E. Teschendorff et al.

BMC BIOINFORMATICS (2017)

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Cell-free DNA Comprises an In Vivo Nucleosome Footprint that Informs Its Tissues-Of-Origin

Matthew W. Snyder et al.

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Integrated digital error suppression for improved detection of circulating tumor DNA

Aaron M. Newman et al.

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Inferring expressed genes by whole-genome sequencing of plasma DNA

Peter Ulz et al.

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Identification of tissue-specific cell death using methylation patterns of circulating DNA

Roni Lehmann-Werman et al.

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Fragment Length of Circulating Tumor DNA

Hunter R. Underhill et al.

PLOS GENETICS (2016)

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Non-random fragmentation patterns in circulating cell-free DNA reflect epigenetic regulation

Maxim Ivanov et al.

BMC GENOMICS (2015)

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Plasma DNA tissue mapping by genome-wide methylation sequencing for noninvasive prenatal, cancer, and transplantation assessments

Kun Sun et al.

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Lengthening and shortening of plasma DNA in hepatocellular carcinoma patients

Peiyong Jiang et al.

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An ultrasensitive method for quantitating circulating tumor DNA with broad patient coverage

Aaron M. Newman et al.

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Chetan Bettegowda et al.

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High-Resolution Profiling of Fetal DNA Clearance from Maternal Plasma by Massively Parallel Sequencing

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CLINICAL CHEMISTRY (2013)

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Liquid biopsy: monitoring cancer-genetics in the blood

Emily Crowley et al.

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DNA methylation arrays as surrogate measures of cell mixture distribution

Eugene Andres Houseman et al.

BMC BIOINFORMATICS (2012)

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The importance of examining the proportion of circulating DNA originating from tumor, microenvironment and normal cells in colorectal cancer patients

Florent Mouliere et al.

EXPERT OPINION ON BIOLOGICAL THERAPY (2012)

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Detection of ultra-rare mutations by next-generation sequencing

Michael W. Schmitt et al.

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High Fragmentation Characterizes Tumour-Derived Circulating DNA

Florent Mouliere et al.

PLOS ONE (2011)

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Detection and quantification of rare mutations with massively parallel sequencing

Isaac Kinde et al.

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Review Oncology

Cell-free nucleic acids as biomarkers in cancer patients

Heidi Schwarzenbach et al.

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Maternal Plasma DNA Sequencing Reveals the Genome-Wide Genetic and Mutational Profile of the Fetus

Y. M. Dennis Lo et al.

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R. Bro et al.

ANALYTICAL AND BIOANALYTICAL CHEMISTRY (2008)

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Deoxyribonuclease activity and circulating DNA concentration in blood plasma of patients with prostate tumors

Anna V. Cherepanova et al.

CIRCULATING NUCLEIC ACIDS IN PLASMA AND SERUM V (2008)

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Circulating mutant DNA to assess tumor dynamics

Frank Diehl et al.

NATURE MEDICINE (2008)

Letter Medical Laboratory Technology

The origin of circulating free DNA

Maniesh van der Vaart et al.

CLINICAL CHEMISTRY (2007)

Article Medical Laboratory Technology

About the possible origin and mechanism of circulating DNA - Apoptosis and active DNA release

M Stroun et al.

CLINICA CHIMICA ACTA (2001)