Rapid and accurate taxonomic classification of short paired-end sequence reads from the 16s ribosomal rna gene
rtax [OPTION]...
-r refd
reference database in FASTA format
-t taxonomy
taxonomy file with sequence IDs matching the reference database
-a queryA
FASTA file containing query sequences (single-ended or read 1)
-b queryB
FASTA file containing query sequences (read b, with matching IDs)
-x
Reverse-complement query A sequences (required if they are provided in the reverse sense)
-y
Reverse-complement query B sequences (required if they are provided in the reverse sense)
-i regex
regular expression used to select part of the fasta header to use as the sequence id. Default: "(\S+)"
-l file
text file containing sequence IDs to process, one per line
-d delimiter
delimiter separating the two reads when provided in a single file
-m tempdir
temporary directory. Will be removed on successful completion, but likely not if there is an error.
-f
for sequences where only one read is available, fall back to single-ended classification. Default: drop these sequences.
-g
for sequences where one read is overly generic, do not fall back to single-ended classification. Default: classify these sequences based on only the more specific read.
-o classifications.out
output path
A quickstart example can be found here: http://dev.davidsoergel.com/trac/rtax/wiki/QuickStart
Rtax can also be used within QIIME workflows, se this link for more information: http://www.qiime.org/tutorials/rtax.html
This manual page was written by Simon Kainz <[email protected]> for the rtax package.
Rtax was written by David A. W. Soergel <[email protected]>.