PARSNP(1)

NAME
parsnp - rapid core genome multi-alignment

DESCRIPTION
|--Parsnp 1.5.6--| For detailed documentation please see --> http://harvest.readthedocs.org/en/latest usage: parsnp [-h] [-c] -d SEQUENCES [SEQUENCES ...] [-r REFERENCE]

    [-g GENBANK [GENBANK ...]] [-o OUTPUT_DIR] [-q QUERY] [-U MAX_MUMI_DISTR_DIST | -mmd MAX_MUMI_DISTANCE] [-F] [-M] [--use-ani] [--min-ani MIN_ANI] [--use-mash] [--max-mash-dist MAX_MASH_DIST] [-a MIN_ANCHOR_LENGTH] [-m MUM_LENGTH] [-C MAX_CLUSTER_D] [-z MIN_CLUSTER_SIZE] [-D MAX_DIAG_DIFF] [-n {mafft,muscle,fsa,prank}] [-u] [--use-fasttree] [--vcf] [-p THREADS] [-P MAX_PARTITION_SIZE] [-v] [-x] [-i INIFILE] [-e] [-V]

    Parsnp quick start for three example scenarios: 1) With reference & genbank file: python Parsnp.py -g <reference_genbank_file1 reference_genbank_file2 ...> -d <seq_file1 seq_file2 ...> -p <threads>

    2) With reference but without genbank file: python Parsnp.py -r <reference_genome> -d <seq_file1 seq_file2 ...> -p <threads>

    3) Autorecruit reference to a draft assembly: python Parsnp.py -q <draft_assembly> -d <seq_file1 seq_file2 ...> -p <threads>

  optional arguments:

-h, --help
    show this help message and exit

  Input/Output:

-c, --curated
    (c)urated genome directory, use all genomes in dir and ignore MUMi?

-d SEQUENCES [SEQUENCES ...], --sequences SEQUENCES [SEQUENCES ...]
    A list of files containing genomes/contigs/scaffolds

-r REFERENCE, --reference REFERENCE
    (r)eference genome (set to ! to pick random one from sequence dir)

-g GENBANK [GENBANK ...], --genbank GENBANK [GENBANK ...]
    A list of Genbank file(s) (gbk)

-o OUTPUT_DIR, --output-dir OUTPUT_DIR

-q QUERY, --query QUERY
    Specify (assembled) query genome to use, in addition to genomes found in genome dir

  MUMi:

-U MAX_MUMI_DISTR_DIST, --max-mumi-distr-dist MAX_MUMI_DISTR_DIST, --MUMi MAX_MUMI_DISTR_DIST
    Max MUMi distance value for MUMi distribution

-mmd MAX_MUMI_DISTANCE, --max-mumi-distance MAX_MUMI_DISTANCE
    Max MUMi distance (default: autocutoff based on distribution of MUMi values)

-F, --fastmum
    Fast MUMi calculation

-M, --mumi_only, --onlymumi
    Calculate MUMi and exit? overrides all other choices!

--use-ani
    Use ani for genome recruitment

--min-ani MIN_ANI
    Min ANI value to allow for genome recruitment.

--use-mash
    Use mash for genome recruitment

--max-mash-dist MAX_MASH_DIST
    Max mash distance.

  MUM search:

-a MIN_ANCHOR_LENGTH, --min-anchor-length MIN_ANCHOR_LENGTH, --anchorlength MIN_ANCHOR_LENGTH
    Min (a)NCHOR length (default = 1.1*(Log(S)))

-m MUM_LENGTH, --mum-length MUM_LENGTH, --mumlength MUM_LENGTH
    Mum length

-C MAX_CLUSTER_D, --max-cluster-d MAX_CLUSTER_D, --clusterD MAX_CLUSTER_D
    Maximal cluster D value

-z MIN_CLUSTER_SIZE, --min-cluster-size MIN_CLUSTER_SIZE, --minclustersize MIN_CLUSTER_SIZE
    Minimum cluster size

  LCB alignment:

-D MAX_DIAG_DIFF, --max-diagonal-difference MAX_DIAG_DIFF, --DiagonalDiff MAX_DIAG_DIFF
    Maximal diagonal difference. Either percentage (e.g. 0.2) or bp (e.g. 100bp)

-n {mafft,muscle,fsa,prank}, --alignment-program {mafft,muscle,fsa,prank}, --alignmentprog {mafft,muscle,fsa,prank}
    Alignment program to use

-u, --unaligned
    Ouput unaligned regions

  Misc:

--use-fasttree
    Use fasttree instead of RaxML

--vcf
    Generate VCF file.

-p THREADS, --threads THREADS
    Number of threads to use

-P MAX_PARTITION_SIZE, --max-partition-size MAX_PARTITION_SIZE
    Max partition size (limits memory usage)

-v, --verbose
    Verbose output

-x, --xtrafast

-i INIFILE, --inifile INIFILE, --ini-file INIFILE

-e, --extend

-V, --version
    show program's version number and exit

AUTHOR
 This manpage was written by Nilesh Patra for the Debian distribution and
 can be used for any other usage of the program.