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。Family reunion via error correction: an efficient analysis of duplex sequencing data
Nicholas Stoler et al.
BMC BIOINFORMATICS (2020)
Alignment-free clustering of UMI tagged DNA molecules
Baraa Orabi et al.
BIOINFORMATICS (2019)
Enhancing the accuracy of next-generation sequencing for detecting rare and subclonal mutations
Jesse J. Salk et al.
NATURE REVIEWS GENETICS (2018)
Targeted genome fragmentation with CRISPR/Cas9 enables fast and efficient enrichment of small genomic regions and ultra-accurate sequencing with low DNA input (CRISPR-DS)
Daniela Nachmanson et al.
GENOME RESEARCH (2018)
UMI-tools: modeling sequencing errors in Unique Molecular Identifiers to improve quantification accuracy
Tom Smith et al.
GENOME RESEARCH (2017)
Artifactual mutations resulting from DNA lesions limit detection levels in ultrasensitive sequencing applications
Barbara Arbeithuber et al.
DNA RESEARCH (2016)
Streamlined analysis of duplex sequencing data with Du Novo
Nicholas Stoler et al.
GENOME BIOLOGY (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)
Trimmomatic: a flexible trimmer for Illumina sequence data
Anthony M. Bolger et al.
BIOINFORMATICS (2014)
Single molecule molecular inversion probes for targeted, high-accuracy detection of low-frequency variation
Joseph B. Hiatt et al.
GENOME 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)
Ultra-Sensitive Sequencing Reveals an Age-Related Increase in Somatic Mitochondrial Mutations That Are Inconsistent with Oxidative Damage
Scott R. Kennedy et al.
PLOS GENETICS (2013)
Massively Parallel Haplotyping on Microscopic Beads for the High-Throughput Phase Analysis of Single Molecules
Jerome Boulanger et al.
PLOS ONE (2012)
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)
Multiplex Targeted Sequencing Identifies Recurrently Mutated Genes in Autism Spectrum Disorders
Brian J. O'Roak et al.
SCIENCE (2012)
Accurate sampling and deep sequencing of the HIV-1 protease gene using a Primer ID
Cassandra B. Jabara et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2011)
Manipulation of FASTQ data with Galaxy
Daniel Blankenberg et al.
BIOINFORMATICS (2010)
Bias and artifacts in multitemplate polymerase chain reactions (PCR)
T Kanagawa
JOURNAL OF BIOSCIENCE AND BIOENGINEERING (2003)