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Cross-linking and immunoprecipitation (CLIP, or CLIP-seq) is a method used in molecular biology that combines UV crosslinking with immunoprecipitation in order to identify RNA binding sites of proteins on a transcriptome-wide scale, thereby increasing our understanding of post-transcriptional regulatory networks. CLIP can be used either with antibodies…
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rna clip sites binding iclip immunoprecipitation proteins cross-linking protein eclip using cells also used par-clip uv crosslinking sequencing interactions identify
| Subject | Predicate | Object | Confidence | Src |
|---|---|---|---|---|
| iCLIP to increase the resolution of the method. cDNA is then synthesized via RT-PCR followed by high-throughput sequencing followed by mapping the reads back to the transcriptome | instance of | which is exploited in variants | 0.80 | text |
| other computational analyses to study the interaction sites | instance of | which is exploited in variants | 0.80 | text |
| eCLIP | instance of | These innovations of iCLIP were adopted by later variants of CLIP | 0.80 | text |
| irCLIP | instance of | These innovations of iCLIP were adopted by later variants of CLIP | 0.80 | text |
| m6A. eCLIP datasets have been produced for over 150 RBPs with validated commercially available antibodies.Other CLIP methodssCLIP | instance of | PCR amplification is then used to obtain sufficient material for high-throughput sequencing. eCLIP can also be used to identify miRNA targets and profile RNA modifications | 0.80 | text |
| m6A. eCLIP datasets have been produced for over 150 RBPs with validated commercially available antibodies | instance of | PCR amplification is then used to obtain sufficient material for high-throughput sequencing. eCLIP can also be used to identify miRNA targets and profile RNA modifications | 0.80 | text |
| RIP have been demonstrated to be dependent on the reaction conditions of the experiment | instance of | The data specificity obtained using early immunoprecipitation methods | 0.80 | text |
| such as protein concentrations | instance of | The data specificity obtained using early immunoprecipitation methods | 0.80 | text |
| ionic conditions | instance of | The data specificity obtained using early immunoprecipitation methods | 0.80 | text |
| and reassociation of RNA-binding proteins following cell lysis could lead to detection of artificial interactions | instance of | The data specificity obtained using early immunoprecipitation methods | 0.80 | text |
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