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Observed mapping statistics are similar to those reported in previous RNA sequencing studies [ 30, 31].
Read mapping statistics are supplied in Table S1 (Additional file 1: Table S1).
The reads were preprocessed and mapped to the reference genome catalogue as described previously [ 15] (mapping statistics are shown in Additional file 2: Table S2).
Point #1: The detailed information about the number of reads acquired for each sample and the read mapping statistics are now provided (see the Materials and methods).
The mapping statistics are summarized in Table 3: 61% of the reads were mapped (49% uniquely mapped and 12% as multimapped reads).
Read mapping statistics are detailed in Table S1 in Additional File 1. Number of mapped reads per kilobase of gene length used in Fisher's exact test calculation are based on IsoEM FPKMs.
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A summary of the genome assembly and mapping statistics is given in Table 2.
A summary of the read mapping statistics is presented in Additional file 5.
An overview of sequencing and mapping statistics is presented in (Additional file 5: Table S1).
MinION Mapping statistics were calculated using count-errors.py [ 29], modified slightly to work with our read IDs.
PCR amplification can lead to a BisSeq library that includes duplicates in the mapping statistics being unrepresentative of the initial BisSeq library.
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