Provided by: centrifuge_1.0.4.2-1_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. centrifuge 1.0.3 October 2021 CENTRIFUGE(1)