Provided by: centrifuge_1.0.3-11_amd64
NAME
centrifuge - rapid and memory-efficient system for classification of DNA sequences
DESCRIPTION
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
AUTHOR
This manpage was written by Andreas Tille for the Debian distribution and can be used for any other usage of the program.