fastq-join - ea-utils: join two paired-end reads on the overlapping ends

       fastq-join: invalid option -- 'h' Unknown option `-h'.

       Joins two paired-end reads on the overlapping ends.

       fastq-join - ea-utils: join two paired-end reads on the overlapping ends

-o FIL     See 'Output' below -v C       Verifies that the 2 files probe id's match up to char C

              use ' ' (space) for Illumina reads

       -p  N        N-percent  maximum difference (8) -m N       N-minimum overlap (6) -r FIL     Verbose stitch
       length report -R         No reverse complement -x         Allow insert < read length

       Output:

              You can supply 3 -o arguments, for un1, un2, join files, or one

       argument as a file name template.  The suffix 'un1, un2, or join'  is  appended  to  the  file,  or  they
       replace a %-character if present.

              If a 'mate' input file is present (barcode read), then the files

       'un3' and 'join2' are also created.

fastq-join 1.1.2                                    July 2015                                      FASTQ-JOIN(1)

fastq-join [options] <read1.fq><read2.fq> [mate.fq] -o<read.%.fq>