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。DNA damage is a pervasive cause of sequencing errors, directly confounding variant identification
Lixin Chen et al.
SCIENCE (2017)
Characterization of the interplay between DNA repair and CRISPR/Cas9-induced DNA lesions at an endogenous locus
Anne Bothmer et al.
NATURE COMMUNICATIONS (2017)
Methods for Optimizing CRISPR-Cas9 Genome Editing Specificity
Josh Tycko et al.
MOLECULAR CELL (2016)
Detecting DNA double-stranded breaks in mammalian genomes by linear amplification-mediated high-throughput genome-wide translocation sequencing
Jiazhi Hu et al.
NATURE PROTOCOLS (2016)
Basal exon skipping and genetic pleiotropy: A predictive model of disease pathogenesis
Theodore G. Drivas et al.
SCIENCE TRANSLATIONAL MEDICINE (2015)
Quantifying on- and off-target genome editing
Ayal Hendel et al.
TRENDS IN BIOTECHNOLOGY (2015)
Comparison of T7E1 and Surveyor Mismatch Cleavage Assays to Detect Mutations Triggered by Engineered Nucleases
Lena Vouillot et al.
G3-GENES GENOMES GENETICS (2015)
Genome-wide detection of DNA double-stranded breaks induced by engineered nucleases
Richard L. Frock et al.
NATURE BIOTECHNOLOGY (2015)
Tn5 transposase and tagmentation procedures for massively scaled sequencing projects
Simone Picelli et al.
GENOME RESEARCH (2014)
Chromosomal Translocations in Human Cells Are Generated by Canonical Nonhomologous End-Joining
Hind Ghezraoui et al.
MOLECULAR CELL (2014)
Anchored multiplex FOR for targeted next-generation sequencing
Zongli Zheng et al.
NATURE MEDICINE (2014)
Easy quantitative assessment of genome editing by sequence trace decomposition
Eva K. Brinkman et al.
NUCLEIC ACIDS RESEARCH (2014)
Integrative Genomics Viewer (IGV): high-performance genomics data visualization and exploration
Helga Thorvaldsdottir et al.
BRIEFINGS IN BIOINFORMATICS (2013)
Tagmentation-based whole-genome bisulfite sequencing
Qi Wang et al.
NATURE PROTOCOLS (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)
Fast gapped-read alignment with Bowtie 2
Ben Langmead et al.
NATURE METHODS (2012)
Genome-wide Translocation Sequencing Reveals Mechanisms of Chromosome Breaks and Rearrangements in B Cells
Roberto Chiarle et al.
CELL (2011)
Integrative genomics viewer
James T. Robinson et al.
NATURE BIOTECHNOLOGY (2011)
Rapid, low-input, low-bias construction of shotgun fragment libraries by high-density in vitro transposition
Andrew Adey et al.
GENOME BIOLOGY (2010)
The Sequence Alignment/Map format and SAMtools
Heng Li et al.
BIOINFORMATICS (2009)
Mutations in the CEP290 (NPHP6) gene are a frequent cause of leber congenital amaurosis
Anneke I. den Hollander et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2006)