Provided by: last-align_1460-1_amd64
NAME
last-train - Try to find suitable score parameters for aligning the given sequences
SYNOPSIS
last-train [options] lastdb-name sequence-file(s)
DESCRIPTION
Try to find suitable score parameters for aligning the given sequences.
OPTIONS
-h, --help show this help message and exit -v, --verbose show more details of intermediate steps Training options: --revsym force reverse-complement symmetry --matsym force symmetric substitution matrix --gapsym force insertion/deletion symmetry --pid=PID skip alignments with > PID% identity (default: 100) --postmask=NUMBER skip mostly-lowercase alignments (default=1) --sample-number=N number of random sequence samples (default: 20000 if --codon else 500) --sample-length=L length of each sample (default: 2000) --scale=S output scores in units of 1/S bits --codon DNA queries & protein reference, with frameshifts Initial parameter options: -r SCORE match score (default: 6 if Q>=1, or 5 if DNA, or 12) -q COST mismatch cost (default: 18 if Q>=1, or 5 if DNA, or 7) -p NAME match/mismatch score matrix -a COST gap existence cost (default: 21 if Q>=1, else 15) -b COST gap extension cost (default: 9 if Q>=1, else 3) -A COST insertion existence cost -B COST insertion extension cost -F LIST frameshift probabilities: del-1,del-2,ins+1,ins+2 (default: 1-b,1-b,1-B,1-B) Alignment options: -D LENGTH query letters per random alignment (default: 1e6) -E EG2 maximum expected alignments per square giga -s STRAND 0=reverse, 1=forward, 2=both (default: 2 if DNA, else 1) -S NUMBER score matrix applies to forward strand of: 0=reference, 1=query (default: 1) -C COUNT omit gapless alignments in COUNT others with > scoreper-length -T NUMBER type of alignment: 0=local, 1=overlap (default: 0) -R DIGITS lowercase & simple-sequence options -m COUNT maximum initial matches per query position (default: 10) -k STEP use initial matches starting at every STEP-th position in each query (default: 1) -P THREADS number of parallel threads -X NUMBER N/X is ambiguous in: 0=neither sequence, 1=reference, 2=query, 3=both (default=0) -Q NAME input format: fastx, sanger (default=fasta)