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GT-READJOINER-PREF(1) | GenomeTools Manual | GT-READJOINER-PREF(1) |
NAME¶
gt-readjoiner-prefilter - Remove contained and low-quality reads and encode read set in GtEncseq format.SYNOPSIS¶
gt readjoiner prefilter [option ...]DESCRIPTION¶
-readset [string]specify the readset name default: filename of first input
sequence_file
-db
specify a list of input libraries (Fasta/FastQ); for
single-end libraries use the filename (which is not allowed to contain
: symbols); for paired-end libraries with reads interleaved
(f,r,f,r,...) in a single file use the notation
<filename>:<insertlength>[,<stdev>] (stdev may be omitted);
for paired-end with reads in two files (f, r) use the notation
<file_f>:<file_r>:<insertlength>[,<stdev>]
-v [yes|no]
be verbose (default: no)
-q [yes|no]
suppress standard output messages (default: no)
-des [yes|no]
store Fasta IDs (or entire descriptionsif used together
with -clipdes no) warning: increases the memory requirement (default:
no)
-clipdes [yes|no]
clip Fasta descriptions after first space set to false if
you need entire descriptions (default: yes)
-memdes [yes|no]
use memory storage for descriptions (default: use
temporary disk storage)
-maxlow [value]
maximal number of low-quality positions in a read
default: infinite
-lowqual [value]
maximal quality for a position to be considered
low-quality (default: 3)
-phred64 [yes|no]
use phred64 scores for FastQ format (default: no)
-help
display help for basic options and exit
-help+
display help for all options and exit
-version
display version information and exit
REPORTING BUGS¶
Report bugs to https://github.com/genometools/genometools/issues.07/29/2020 | GenomeTools 1.6.1 |