Provided by: kmerresistance_2.2.0-3ubuntu1_amd64
NAME
kmerresistance - correlates mapped genes with the predicted species of WGS samples
SYNOPSIS
DESCRIPTION
KmerResistance correlates mapped genes with the predicted species of WGS samples, where this this allows for identification of genes in samples which have been poorly sequenced or high accuracy predictions for samples with contamination. KmerResistance has one dependency, namely KMA to perform the mapping, which is also freely available.
OPTIONS
-i Input/query file name REQUIRED -o Output file REQUIRED -t_db Template DB REQUIRED -s_db Species DB REQUIRED -id ID threshhold 70.0 -dct Depth correction threshhold 0.1 -kma alternative KMA kma KMA options: -i Input/query file name None REQUIRED -o Output file None REQUIRED -t_db Template DB None REQUIRED -k Kmersize 16 -e evalue 0.05 -delta Align in pieces of delta 511 -mem_mode Use kmers to choose best template, and save memory False -ex_mode Searh kmers exhaustively False -deCon Remove contamination False -dense Do not allow insertions in assembly False -ref_fsa Consensus sequnce will have "n" instead of gaps False -matrix Print assembly matrix False -mp Minimum phred score 30 -5p Cut a constant number of nucleotides from the 5 prime. 0 -Sparse Run KmerFinder False -ID Minimum ID 1.0% -ss Sparse sorting (q,c,d) q -shm Use shared DB made by kma_shm 0 (lvl) -swap Swap DB to disk 0 (lvl) -1t1 Skip HMM False -boot Bootstrap sequence False -mrs Minimum alignment score, normalized to alignment length 0.5 -reward Score for match 1 -penalty Penalty for mismatch -2 -gapopen Penalty for gap opening -3 -gapextend Penalty for gap extension -1 -h Shows this help message
EXAMPLES
Mapping reads against resistance genes: kmerresistance -i sample_1.fastq sample_2.fastq -o out -t_db ResFinder -s_db bacteria
AUTHOR
This manpage was written by Andreas Tille for the Debian distribution and can be used for any other usage of the program.