Regarding the tool structurefold, iterative mapping on Galaxy accepts one fastq at a time as input, it does not support alignment for paired end reads. Then bowtie runs on read1 and read2 separately producing 2 bam files. Is this ok? How to proceed with 2 bam files for the next modules? Or should I upload merged fastq files for paired-end reads?
Question: Structurefold Iterative Mapping Input Fastq
18 months ago by
bounlu • 0
bounlu • 0 wrote:
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