FRASER
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ERROR: Paired-end reads were detected in single-end read library
Dear sir, I tried to use fds<- countRNAData(fds) to count my bam file. There are something wrong when running Subread: ERROR: Paired-end reads were detected in single-end read library : /NGS_Storage/Debbie/Tumor/A3060/arriba/Aligned.sortedByCoord.out.bam No counts were generated. Error: BiocParallel errors 1 remote errors, element index: 1 0 unevaluated and other errors first remote error:
Should I add any option? or I should direct use Subread?