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updated docs
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tyjo committed Jun 25, 2021
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Expand Up @@ -166,7 +166,8 @@ The input can either be a single fastq file, or a folder of fastq files to map.
It also takes an optional ``--threads`` argument that allows bowtie2 to use
multiple threads. Reads are output as ``bam`` files to save space.

For paired end sequencing, it is recommend to only map reads from a single mate-pair.
For paired-end sequencing, we recommand mapping reads from end only (e.g. the files
ending in either _1.* or _2.*).


Merging mapped reads from multiple indexes
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