Provided by: tnseq-transit_3.3.12-1_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.
transit-tpp 3.1.0 August 2020 TRANSIT-TPP(1)