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RNA-Seq data analysis and abundance of human iGluR transcripts. A Alignment of individual cDNA reads to a reference genome provides direct information on splice junctions and single-nucleotide mismatches. B Single-nucleotide coverage of the canonical iGluR exons over all 35 analyzed datasets (Table S1–3). Short bars indicate the coverage of individual exons; red and blue bars indicate 5′- and 3′-exons, respectively. Longer bars show the corresponding mean
