Related references
Note: Only part of the references are listed.Single-strand specific nuclease enhances accuracy of error-corrected sequencing and improves rare mutation-detection sensitivity
Yuki Otsubo et al.
ARCHIVES OF TOXICOLOGY (2022)
Somatic mutation landscapes at single-molecule resolution
Federico Abascal et al.
NATURE (2021)
Tumor-Infiltrating Lymphocytes, Tumor Mutational Burden, and Genetic Alterations in Microsatellite Unstable, Microsatellite Stable, or Mutant POLE/POLD1 Colon Cancer
Ajaratu Keshinro et al.
JCO PRECISION ONCOLOGY (2021)
Distinctive genomic characteristics in POLE/POLD1-mutant cancers can potentially predict beneficial clinical outcomes in patients who receive immune checkpoint inhibitor
Junjun He et al.
ANNALS OF TRANSLATIONAL MEDICINE (2021)
SinoDuplex: An Improved Duplex Sequencing Approach to Detect Low-frequency Variants in Plasma cfDNA Samples
Yongzhe Ren et al.
GENOMICS PROTEOMICS & BIOINFORMATICS (2020)
The mutational constraint spectrum quantified from variation in 141,456 humans
Konrad J. Karczewski et al.
NATURE (2020)
Detection of genome-wide low-frequency mutations with Paired-End and Complementary Consensus Sequencing (PECC-Seq) revealed end-repair-derived artifacts as residual errors
Xinyue You et al.
ARCHIVES OF TOXICOLOGY (2020)
Why Formalin-fixed, Paraffin-embedded Biospecimens Must Be Used in Genomic Medicine: An Evidence-based Review and Conclusion
William Mathieson et al.
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY (2020)
Direct quantification of in vivo mutagenesis and carcinogenesis using duplex sequencing
Charles C. Valentine et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2020)
Use of FFPE-derived DNA in next generation sequencing: DNA extraction methods
Samantha J. McDonough et al.
PLOS ONE (2019)
Sources of erroneous sequences and artifact chimeric reads in next generation sequencing of genomic DNA from formalin-fixed paraffin-embedded samples
Simon Haile et al.
NUCLEIC ACIDS RESEARCH (2019)
Targeted Single Primer Enrichment Sequencing with Single End Duplex-UMI
Quan Peng et al.
SCIENTIFIC REPORTS (2019)
Next-Generation Sequencing Using S1 Nuclease for Poor-Quality Formalin-Fixed, Paraffin-Embedded Tumor Specimens
Sung-Min Chun et al.
JOURNAL OF MOLECULAR DIAGNOSTICS (2018)
A Specific Mutational Signature Associated with DNA 8-Oxoguanine Persistence in MUTYH-defective Colorectal Cancer
Alessandra Viel et al.
EBIOMEDICINE (2017)
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)
Sequence Artifacts in DNA from Formalin-Fixed Tissues: Causes and Strategies for Minimization
Hongdo Do et al.
CLINICAL CHEMISTRY (2015)
Reducing Sequence Artifacts in Amplicon-Based Massively Parallel Sequencing of Formalin-Fixed Paraffin-Embedded DNA by Enzymatic Depletion of Uracil-Containing Templates
Hongdo Do et al.
CLINICAL CHEMISTRY (2013)
Germline and somatic polymerase ε and δ mutations define a new class of hypermutated colorectal and endometrial cancers
Sarah Briggs et al.
JOURNAL OF PATHOLOGY (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)
The Sequence Alignment/Map format and SAMtools
Heng Li et al.
BIOINFORMATICS (2009)
Fast and accurate short read alignment with Burrows-Wheeler transform
Heng Li et al.
BIOINFORMATICS (2009)
Share Paper
