| Literature DB >> 33584810 |
Matthew J Rybin1,2, Melina Ramic1,2, Natalie R Ricciardi1,2, Philipp Kapranov3, Claes Wahlestedt1,2, Zane Zeier1,2.
Abstract
Genome instability is associated with myriad human diseases and is a well-known feature of both cancer and neurodegenerative disease. Until recently, the ability to assess DNA damage-the principal driver of genome instability-was limited to relatively imprecise methods or restricted to studying predefined genomic regions. Recently, new techniques for detecting DNA double strand breaks (DSBs) and single strand breaks (SSBs) with next-generation sequencing on a genome-wide scale with single nucleotide resolution have emerged. With these new tools, efforts are underway to define the "breakome" in normal aging and disease. Here, we compare the relative strengths and weaknesses of these technologies and their potential application to studying neurodegenerative diseases.Entities:
Keywords: DNA damage; aging; double strand break (DSB); genome instability; neurodegeneration; neurodegenerative disease; single strand break (SSB)
Year: 2021 PMID: 33584810 PMCID: PMC7873462 DOI: 10.3389/fgene.2020.610386
Source DB: PubMed Journal: Front Genet ISSN: 1664-8021 Impact factor: 4.599