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BLESS, also known as breaks labeling, enrichment on streptavidin and next-generation sequencing, is a method used to detect genome-wide double-strand DNA damage. In contrast to chromatin immunoprecipitation (ChIP)-based methods of identifying DNA double-strand breaks (DSBs) by labeling DNA repair proteins, BLESS utilizes biotinylated DNA linkers to…
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dna dsbs breaks biotinylated linker labeling streptavidin genome enrichment sequencing methods using also beads distal analysis biotin specific sample double-stranded
| Subject | Predicate | Object | Confidence | Src |
|---|---|---|---|---|
| yeast cells | instance of | A limitation of the original BLESS method is that it is problematic in application to smaller cells | 0.80 | text |
| CRISPR-Cas9 or TALEN | instance of | specific DSB-mapping methods like BLESS are useful for breakome surveys.DSBs can be artificially induced using genome editing technologies | 0.80 | text |
| BLESS | has application | While | 0.60 | section |
| BLESS | has application | DNA | 0.60 | section |
| BLESS | has application | For | 0.60 | section |
| BLESS | has application | DSB-mapping | 0.60 | section |
| BLESS | has application | DSBs | 0.60 | section |
| BLESS | has application | CRISPR-Cas9 | 0.60 | section |
| BLESS | has application | TALEN | 0.60 | section |
| BLESS | has application | These | 0.60 | section |
| BLESS | has application | Since BLESS | 0.60 | section |
| BLESS | related to Advantages | Use | 0.60 | section |
These clusters group vocabulary that occurs around closely connected concepts in the source material.
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