BLISS is a versatile and quantitative method for genome-wide profiling of DNA double-strand breaks

Yan, Winston X., Mirzazadeh, Reza, Garnerone, Silvano, Scott, David, Schneider, Martin W., Kallas, Tomasz, Custodio, Joaquin, Wernersson, Erik, Li, Yinqing, Gao, Linyi, Federova, Yana, Zetsche, Bernd, Zhang, Feng, Bienko, Magda, Crosetto, Nicola·2017·Nature Communications
DOI 10.1038/ncomms15058

Cited by (369)

Items 301–369 of 369

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  11. ChromInSight: Revealing DNA Double‐Strand Breaks Through Chromatin Structural Insights With an Interpretable Graph Neural Network Framework
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  17. ERCC1-XPF Interacts with Topoisomerase IIβ to Facilitate the Repair of Activity-induced DNA Breaks
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  19. Engineered PAM-flexible FnCas9 variants for robust and specific genome editing and diagnostics
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  20. Massively parallel genomic perturbations with multi-target CRISPR reveal new insights on Cas9 activity and DNA damage responses at endogenous sites
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  21. Optimization of NLS Composition Improves CRISPR-Cas12a Editing Rates in Human Primary Cells
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  22. Specificity of CRISPR‐Cas9 Gene Editing
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  23. Target-matched increased fidelity SpCas9 variants can edit any target without genome-wide off-target effects
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  24. Detection and Quantification of Genome Editing Events in Preclinical and Clinical Studies
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  25. Joint single-cell capture of Cas9 edits and transcriptomes reveals on- and off-target effects on gene expression
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  26. qDSB-Seq: quantitative DNA double-strand break sequencing
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  27. Generating Isogenic Models of Li-Fraumeni Syndrome and Restoring p53 using CRISPR
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  30. Faculty Opinions recommendation of GPSeq reveals the radial organization of chromatin in the cell nucleus.
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  36. Sensitivity of DNA double-strand break loci is coupled with spatial interaction density of chromatin
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  37. Bioinformatics tools and databases in genome editing for plants
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  38. Additional file 2 of A graph neural network-based interpretable framework reveals a novel DNA fragility–associated chromatin structural unit
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  40. DNA Damage, Repair, and Advanced DNA Damage Detection Technologies
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  41. Precise Mapping of Physiological DSBs Using In-Suspension Break Labeling In Situ and Sequencing (sBLISS)
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  42. Development of new increased fidelity SpCas9 variants
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  47. Genome Editing as Genetic Engineering Tool: Potential Applications in Production of Microbial Foods for Food Security
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  50. Additional file 2 of ITR-Seq, a next-generation sequencing assay, identifies genome-wide DNA editing sites in vivo following adeno-associated viral vector-mediated genome editing
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  51. Additional file 3 of A graph neural network-based interpretable framework reveals a novel DNA fragility–associated chromatin structural unit
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  54. Additional file 2 of CasKAS: direct profiling of genome-wide dCas9 and Cas9 specificity using ssDNA mapping
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