Mapping DNA Breaks by Next-Generation Sequencing
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Publisher
Springer New York
Link
http://link.springer.com/content/pdf/10.1007/978-1-4939-7306-4_13
Reference19 articles.
1. Iacovoni JS et al (2010) High-resolution profiling of gammaH2AX around DNA double strand breaks in the mammalian genome. EMBO J 29(8):1446–1457
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3. Hu J et al (2016) Detecting DNA double-stranded breaks in mammalian genomes by linear amplification-mediated high-throughput genome-wide translocation sequencing. Nat Protoc 11(5):853–871
4. Klein IA et al (2011) Translocation-capture sequencing reveals the extent and nature of chromosomal rearrangements in B lymphocytes. Cell 147(1):95–106
5. Chiarle R et al (2011) Genome-wide translocation sequencing reveals mechanisms of chromosome breaks and rearrangements in B cells. Cell 147(1):107–119
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