-u, --uniq
keep only the best match, remove all matches, if the
second best is not much worse
-q f, --uniqThresh=f
threshold % for uniq, second best must be lower than this
fraction of best to keep the best match (default 0.96)
-b, --best
output all best matches that satisfy minId and
minCover
-e n, --minId=n
minimal percentage of identity (default 92)
-c n, --minCover=n
minimal percentage of coverage of the query read (default
80)
-n, --noIntrons
do not allow longer gaps -for RNA-RNA alignments-
-l n, --insertLimit=n
maximum assumed size of inserts (default 10)
-s n, --maxSortesTest=n
test if input file is sorted by query name for this
number of alignments (default 100000)
-p, --paired
require that paired reads are on opposite strands of same
target. Requires alignment names to contain the suffixes /1,/2 or /f,/r.
-w, --pairwiseAlignments
use in case alignments were done in pairwise
fashion
-x n, --maxIntronLen=n
maximal separation of paired reads (default 500000)
-d file, --pairBedFile=file
file name of pairedness coverage: a BED format file in
which for each position the number of filtered read pairs is reported that
contain the position in or between the reads
-g file, --commonGeneFile=file
file name in which to write cases where one read maps
several different genes
-t n, --threads=n
use n threads for compression/decompression (default 1);
available only if library SeqLib >= 1.2 is used
-v, --verbose
output debugging info
-h, --help
produce help message.