Provided by: parsnp_1.6.2+dfsg-1_amd64
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.