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clustalo(clustal omega) 帮助文档

clustalo(clustal omega) 帮助文档

作者: 喜欢吃土豆的彭某人 | 来源:发表于2020-08-25 22:04 被阅读0次

    clustalo -h

    Clustal Omega - 1.2.4 (AndreaGiacomo)

    If you like Clustal-Omega please cite:

    Sievers F, Wilm A, Dineen D, Gibson TJ, Karplus K, Li W, Lopez R, McWilliam H, Remmert M, Söding J, Thompson JD, Higgins DG.

    Fast, scalable generation of high-quality protein multiple sequence alignments using Clustal Omega.

    Mol Syst Biol. 2011 Oct 11;7:539. doi: 10.1038/msb.2011.75. PMID: 21988835.

    If you don't like Clustal-Omega, please let us know why (and cite us anyway).

    Check http://www.clustal.org for more information and updates.

    Usage: clustalo [-hv] [-i {<file>,-}] [--hmm-in=<file>]... [--hmm-batch=<file>] [--dealign] [--profile1=<file>] [--profile2=<file>] [--is-profile][-t {Protein, RNA, DNA}] [--infmt={a2m=fa[sta],clu[stal],msf,phy[lip],selex,st[ockholm],vie[nna]}] [--distmat-in=<file>] [--distmat-out=<file>] [--guidetree-in=<file>] [--guidetree-out=<file>] [--pileup] [--full] [--full-iter] [--cluster-size=<n>] [--clustering-out=<file>] [--trans=<n>] [--posterior-out=<file>] [--use-kimura] [--percent-id] [-o {file,-}] [--outfmt={a2m=fa[sta],clu[stal],msf,phy[lip],selex,st[ockholm],vie[nna]}] [--residuenumber] [--wrap=<n>] [--output-order={input-order,tree-order}] [--iterations=<n>] [--max-guidetree-iterations=<n>] [--max-hmm-iterations=<n>] [--maxnumseq=<n>] [--maxseqlen=<l>] [--auto] [--threads=<n>] [--pseudo=<file>] [-l <file>] [--version] [--long-version] [--force] [--MAC-RAM=<n>]

    A typical invocation would be: clustalo -i my-in-seqs.fa -o my-out-seqs.fa -v

    See below for a list of all options.

    Sequence Input:

      -i, --in, --infile={<file>,-} Multiple sequence input file (- for stdin)

      --hmm-in=<file>          HMM input files

      --hmm-batch=<file>        specify HMMs for individual sequences

      --dealign                Dealign input sequences

      --profile1, --p1=<file>  Pre-aligned multiple sequence file (aligned columns will be kept fix)

      --profile2, --p2=<file>  Pre-aligned multiple sequence file (aligned columns will be kept fix)

      --is-profile              disable check if profile, force profile (default no)

      -t, --seqtype={Protein, RNA, DNA} Force a sequence type (default: auto)

      --infmt={a2m=fa[sta],clu[stal],msf,phy[lip],selex,st[ockholm],vie[nna]} Forced sequence input file format (default: auto)

    Clustering:

      --distmat-in=<file>      Pairwise distance matrix input file (skips distance computation)

      --distmat-out=<file>      Pairwise distance matrix output file

      --guidetree-in=<file>    Guide tree input file (skips distance computation and guide-tree clustering step)

      --guidetree-out=<file>    Guide tree output file

      --pileup                  Sequentially align sequences

      --full                    Use full distance matrix for guide-tree calculation (might be slow; mBed is default)

      --full-iter              Use full distance matrix for guide-tree calculation during iteration (might be slowish; mBed is default)

      --cluster-size=<n>        soft maximum of sequences in sub-clusters

      --clustering-out=<file>  Clustering output file

      --trans=<n>              use transitivity (default: 0)

      --posterior-out=<file>    Posterior probability output file

      --use-kimura              use Kimura distance correction for aligned sequences (default no)

      --percent-id              convert distances into percent identities (default no)

    Alignment Output:

      -o, --out, --outfile={file,-} Multiple sequence alignment output file (default: stdout)

      --outfmt={a2m=fa[sta],clu[stal],msf,phy[lip],selex,st[ockholm],vie[nna]} MSA output file format (default: fasta)

      --residuenumber, --resno  in Clustal format print residue numbers (default no)

      --wrap=<n>                number of residues before line-wrap in output

      --output-order={input-order,tree-order} MSA output order like in input/guide-tree

    Iteration:

      --iterations, --iter=<n>  Number of (combined guide-tree/HMM) iterations

      --max-guidetree-iterations=<n> Maximum number of guidetree iterations

      --max-hmm-iterations=<n>  Maximum number of HMM iterations

    Limits (will exit early, if exceeded):

      --maxnumseq=<n>          Maximum allowed number of sequences

      --maxseqlen=<l>          Maximum allowed sequence length

    Miscellaneous:

      --auto                    Set options automatically (might overwrite some of your options)

      --threads=<n>            Number of processors to use

      --pseudo=<file>          Input file for pseudo-count parameters

      -l, --log=<file>          Log all non-essential output to this file

      -h, --help                Print this help and exit

      -v, --verbose            Verbose output (increases if given multiple times)

      --version                Print version information and exit

      --long-version            Print long version information and exit

      --force                  Force file overwriting

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