4.8 Article

Detection of low-frequency DNA variants by targeted sequencing of the Watson and Crick strands

Related references

Note: Only part of the references are listed.
Article Biotechnology & Applied Microbiology

Accurate detection of mosaic variants in sequencing data without matched controls

Yanmei Dou et al.

NATURE BIOTECHNOLOGY (2020)

Article Multidisciplinary Sciences

Integrating genomic features for non-invasive early lung cancer detection

Jacob J. Chabon et al.

NATURE (2020)

Article Biochemistry & Molecular Biology

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

Peiyong Jiang et al.

GENOME RESEARCH (2020)

Editorial Material Cell Biology

Applications of liquid biopsies for cancer

Austin K. Mattox et al.

SCIENCE TRANSLATIONAL MEDICINE (2019)

Article Biochemistry & Molecular Biology

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

Pedram Razavi et al.

NATURE MEDICINE (2019)

Article Multidisciplinary Sciences

Targeted Single Primer Enrichment Sequencing with Single End Duplex-UMI

Quan Peng et al.

SCIENTIFIC REPORTS (2019)

Article Multidisciplinary Sciences

Detection and localization of surgically resectable cancers with a multi-analyte blood test

Joshua D. Cohen et al.

SCIENCE (2018)

Review Biochemical Research Methods

Massively parallel sequencing techniques for forensics: A review

Brigitte Bruijns et al.

ELECTROPHORESIS (2018)

Article Biochemistry & Molecular Biology

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

Tom Smith et al.

GENOME RESEARCH (2017)

Review Multidisciplinary Sciences

DNA sequencing at 40: past, present and future

Jay Shendure et al.

NATURE (2017)

Article Multidisciplinary Sciences

Combined circulating tumor DNA and protein biomarker-based liquid biopsy for the earlier detection of pancreatic cancers

Joshua D. Cohen et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2017)

Article Cell Biology

Direct detection of early-stage cancers using circulating tumor DNA

Jillian Phallen et al.

SCIENCE TRANSLATIONAL MEDICINE (2017)

Article Biochemistry & Molecular Biology

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

Matthew W. Snyder et al.

Article Biotechnology & Applied Microbiology

Integrated digital error suppression for improved detection of circulating tumor DNA

Aaron M. Newman et al.

NATURE BIOTECHNOLOGY (2016)

Article Multidisciplinary Sciences

Genome-wide quantification of rare somatic mutations in normal human tissues using massively parallel sequencing

Margaret L. Hoang et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2016)

Article Gastroenterology & Hepatology

A Combination of Molecular Markers and Clinical Features Improve the Classification of Pancreatic Cysts

Simeon Springer et al.

GASTROENTEROLOGY (2015)

Article Genetics & Heredity

Evaluation of Hybridization Capture Versus Amplicon-Based Methods for Whole-Exome Sequencing

Eric Samorodnitsky et al.

HUMAN MUTATION (2015)

Article Biochemical Research Methods

Sequencing small genomic targets with high efficiency and extreme accuracy

Michael W. Schmitt et al.

NATURE METHODS (2015)

Article Multidisciplinary Sciences

Detection of tumor-derived DNA in cerebrospinal fluid of patients with primary tumors of the brain and spinal cord

Yuxuan Wang et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2015)

Article Biochemistry & Molecular Biology

Anchored multiplex FOR for targeted next-generation sequencing

Zongli Zheng et al.

NATURE MEDICINE (2014)

Article Biochemical Research Methods

Detecting ultralow-frequency mutations by Duplex Sequencing

Scott R. Kennedy et al.

NATURE PROTOCOLS (2014)

Article Cell Biology

Detection of Circulating Tumor DNA in Early- and Late-Stage Human Malignancies

Chetan Bettegowda et al.

SCIENCE TRANSLATIONAL MEDICINE (2014)

Article Biochemical Research Methods

Quantifying single nucleotide variant detection sensitivity in exome sequencing

Alison M. Meynert et al.

BMC BIOINFORMATICS (2013)

Review Multidisciplinary Sciences

Cancer Genome Landscapes

Bert Vogelstein et al.

SCIENCE (2013)

Article Multidisciplinary Sciences

Detection of ultra-rare mutations by next-generation sequencing

Michael W. Schmitt et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2012)

Article Multidisciplinary Sciences

Detection and quantification of rare mutations with massively parallel sequencing

Isaac Kinde et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2011)

Article Biochemical Research Methods

The Sequence Alignment/Map format and SAMtools

Heng Li et al.

BIOINFORMATICS (2009)

Article Multidisciplinary Sciences

Sequencing the nuclear genome of the extinct woolly mammoth

Webb Miller et al.

NATURE (2008)

Article Multidisciplinary Sciences

Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma

Rossa W. K. Chiu et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)

Article Medicine, General & Internal

Brief report - The HBV drug entecavir - Effects on HIV-1 replication and resistance

Moira A. McMahon et al.

NEW ENGLAND JOURNAL OF MEDICINE (2007)