Centrifuge version 1.0.3-beta by the Centrifuge developer team (centrifuge.metagenomics@gmail.com) Usage:
centrifuge [options]* -x <cf-idx> {-1 <m1> -2 <m2> | -U <r>} [-S <filename>] [--report-file
<report>]
<cf-idx>
Index filename prefix (minus trailing .X.cf).
<m1> Files with #1 mates, paired with files in <m2>. Could be gzip'ed (extension: .gz) or bzip2'ed
(extension: .bz2).
<m2> Files with #2 mates, paired with files in <m1>. Could be gzip'ed (extension: .gz) or bzip2'ed
(extension: .bz2).
<r> Files with unpaired reads. Could be gzip'ed (extension: .gz) or bzip2'ed (extension: .bz2).
<filename>
File for classification output (default: stdout)
<report>
File for tabular report output (default: centrifuge_report.tsv)
<m1>, <m2>, <r> can be comma-separated lists (no whitespace) and can be specified many times.
E.g. '-U file1.fq,file2.fq -U file3.fq'.
Options (defaults in parentheses):
Input:
-q query input files are FASTQ .fq/.fastq (default)
--qseq query input files are in Illumina's qseq format
-f query input files are (multi-)FASTA .fa/.mfa
-r query input files are raw one-sequence-per-line
-c <m1>, <m2>, <r> are sequences themselves, not files
-s/--skip <int>
skip the first <int> reads/pairs in the input (none)
-u/--upto <int>
stop after first <int> reads/pairs (no limit)
-5/--trim5 <int>
trim <int> bases from 5'/left end of reads (0)
-3/--trim3 <int>
trim <int> bases from 3'/right end of reads (0)
--phred33
qualities are Phred+33 (default)
--phred64
qualities are Phred+64
--int-quals
qualities encoded as space-delimited integers
--ignore-quals
treat all quality values as 30 on Phred scale (off)
--nofw do not align forward (original) version of read (off)
--norc do not align reverse-complement version of read (off)
Classification:--min-hitlen <int>
minimum length of partial hits (default 22, must be greater than 15)
--min-totallen <int>
minimum summed length of partial hits per read (default 0)
--host-taxids <taxids> comma-separated list of taxonomic IDs that will be preferred in classification
--exclude-taxids <taxids> comma-separated list of taxonomic IDs that will be excluded in classification
Output:
--out-fmt <str>
define output format, either 'tab' or 'sam' (tab)
--tab-fmt-cols <str>
columns in tabular format, comma separated default:
readID,seqID,taxID,score,2ndBestScore,hitLength,queryLength,numMatches
-t/--time
print wall-clock time taken by search phases
--un <path>
write unpaired reads that didn't align to <path>
--al <path>
write unpaired reads that aligned at least once to <path>
--un-conc <path>
write pairs that didn't align concordantly to <path>
--al-conc <path>
write pairs that aligned concordantly at least once to <path>
(Note: for --un, --al, --un-conc, or --al-conc, add '-gz' to the option name, e.g. --un-gz
<path>, to gzip compress output, or add '-bz2' to bzip2 compress output.) --quiet
print nothing to stderr except serious errors --met-file <path> send metrics to file at <path>
(off) --met-stderr send metrics to stderr (off) --met <int> report internal
counters & metrics every <int> secs (1)
Performance:
-o/--offrate <int> override offrate of index; must be >= index's offrate
-p/--threads <int> number of alignment threads to launch (1)
--mm use memory-mapped I/O for index; many instances can share
Other:
--qc-filter
filter out reads that are bad according to QSEQ filter
--seed <int>
seed for random number generator (0)
--non-deterministic seed rand. gen. arbitrarily instead of using read attributes
--version
print version information and quit
-h/--help
print this usage message