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, 2010). Our CLIP data now confirmed that Rbfox proteins indeed bind to the expected site in?vivo in the brain ( Figure?1C). To quantitatively compare the RNA binding profiles of different Rbfox family members, we defined a nonredundant set of Rbfox-RNA interaction sites using all unique CLIP tags pooled together (Figure?1D; Experimental Procedures). A stringent set of 41,182 genic CLIP tag clusters with at least one statistically significant peak (p?[http://en.wikipedia.org/wiki/Vasopressin_receptor Vasopressin Receptor] is somewhat lower (R?= 0.76�C0.80; Figure?1F). In addition, we confirmed that the two CLIP protocols gave very reproducible results in the global profiles (R?= 0.97; Figure?1G). Based on these observations, we conclude that the three Rbfox family members have [http://www.selleckchem.com/products/gsk126.html Selleckchem GSK126] similar RNA-interaction profiles on a genome-wide scale, consistent with the notion that their binding specificity is largely determined by their very similar RRMs. Although it remains possible that a small proportion of the binding sites could be preferentially recognized by a specific member, for this work, CLIP tags of all three members were pooled together for further analysis. Using two CLIP protocols in parallel allowed us to employ [http://www.selleckchem.com/products/Erlotinib-Hydrochloride.html buy Erlotinib] different strategies to pinpoint the exact Rbfox-RNA crosslink and interaction sites (Figures 2 and S2). For CLIP tags obtained by the standard protocol, we performed CIMS analysis using our established method (Figure?2A) (Moore et?al., 2014?and?Zhang and Darnell, 2011). Nucleotide deletions were observed in 14% of standard CLIP tags, from which 1,424 reproducible CIMS were identified (false discovery rate [FDR]?