Provided by: tnseq-transit_3.3.4-1_amd64
NAME
transit-tpp - statistical calculations of essentiality of genes or genomic regions
DESCRIPTION
usage: python PATH/src/tpp.py -bwa <EXECUTABLE_WITH_PATH> -ref <fasta-file|comma_separated_list> -reads1 <FASTQ_OR_FASTA_FILE> [-reads2 <FASTQ_OR_FASTA_FILE>] -output <BASE_FILENAME> [OPTIONAL ARGS] OPTIONAL ARGS: -protocol [Sassetti|Tn5|Mme1] # which sample prep protocol was used?; sassetti protocol is the default; this sets the default transposon and primer sequence -primer <seq> # prefix of reads corresponding to end of transposon at junction with genomic sequence; can override default seq -maxreads <INT> -mismatches <INT> # when searching for constant regions in reads 1 and 2; default is 1 -flags "<STRING>" # args to pass to BWA -bwa-alg [aln|mem] # Default: mem. Algorithm to use for mapping reads with bwa -primer-start-window INT,INT # position in read to search for start of primer; default is [0,20] -window-size INT # automatic method to set window -barseq_catalog_in|-barseq_catalog_out <file> -replicon-ids <comma_separated_list_of_names> # if multiple replicons/genomes/contigs/sequences were provided in -ref, give them names. # Enter 'auto' for autogenerated ids.