相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Enhancing the accuracy of next-generation sequencing for detecting rare and subclonal mutations
Jesse J. Salk et al.
NATURE REVIEWS GENETICS (2018)
Mutational signature analysis identifies MUTYH deficiency in colorectal cancers and adrenocortical carcinomas
Camilla Pilati et al.
JOURNAL OF PATHOLOGY (2017)
DNA damage is a pervasive cause of sequencing errors, directly confounding variant identification
Lixin Chen et al.
SCIENCE (2017)
Mutant DNA quantification by digital PCR can be confounded by heating during DNA fragmentation
Qing Kang et al.
BIOTECHNIQUES (2016)
Decreased Mitochondrial Mutagenesis during Transformation of Human Breast Stem Cells into Tumorigenic Cells
Eun Hyun Ahn et al.
CANCER RESEARCH (2016)
Human Cancers Express a Mutator Phenotype: Hypothesis, Origin, and Consequences
Lawrence A. Loeb
CANCER RESEARCH (2016)
Artifactual mutations resulting from DNA lesions limit detection levels in ultrasensitive sequencing applications
Barbara Arbeithuber et al.
DNA RESEARCH (2016)
Integrated digital error suppression for improved detection of circulating tumor DNA
Aaron M. Newman et al.
NATURE BIOTECHNOLOGY (2016)
Coming of age: ten years of next-generation sequencing technologies
Sara Goodwin et al.
NATURE REVIEWS GENETICS (2016)
Sequencing small genomic targets with high efficiency and extreme accuracy
Michael W. Schmitt et al.
NATURE METHODS (2015)
Detection of Ultra-Rare Mitochondrial Mutations in Breast Stem Cells by Duplex Sequencing
Eun Hyun Ahn et al.
PLOS ONE (2015)
Accurate mitochondrial DNA sequencing using off-target reads provides a single test to identify pathogenic point mutations
Helen R. Griffin et al.
GENETICS IN MEDICINE (2014)
Reactive oxygen species, heat stress and oxidative-induced mitochondrial damage. A review
Imen Belhadj Slimen et al.
INTERNATIONAL JOURNAL OF HYPERTHERMIA (2014)
Detecting ultralow-frequency mutations by Duplex Sequencing
Scott R. Kennedy et al.
NATURE PROTOCOLS (2014)
Spatial and Temporal Mapping of De Novo Mutations in Schizophrenia to a Fetal Prefrontal Cortical Network
Suleyman Gulsuner et al.
CELL (2013)
Signatures of mutational processes in human cancer
Ludmil B. Alexandrov et al.
NATURE (2013)
Discovery and characterization of artifactual mutations in deep coverage targeted capture sequencing data due to oxidative DNA damage during sample preparation
Maura Costello et al.
NUCLEIC ACIDS RESEARCH (2013)
High-throughput DNA sequencing errors are reduced by orders of magnitude using circle sequencing
Dianne I. Lou et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2013)
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)
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)
Whole Exome Sequencing and Homozygosity Mapping Identify Mutation in the Cell Polarity Protein GPSM2 as the Cause of Nonsyndromic Hearing Loss DFNB82
Tom Walsh et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2010)
The Sequence Alignment/Map format and SAMtools
Heng Li et al.
BIOINFORMATICS (2009)
Oct4 expression in adult human stem cells: evidence in support of the stem cell theory of carcinogenesis
MH Tai et al.
CARCINOGENESIS (2005)
Oxidative DNA damage: mechanisms, mutation, and disease
MS Cooke et al.
FASEB JOURNAL (2003)
Heat-induced formation of reactive oxygen species and 8-oxoguanine, a biomarker of damage to DNA
VI Bruskov et al.
NUCLEIC ACIDS RESEARCH (2002)