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iva_qc options
You must give paired reads either as two separate files with
-f reads_1.fastq -r reads_2.fastq
or in a single interleaved file with
--fr reads.fastq
You have to either provide a reference genome in the form of a directory of EMBL files with
--embl_dir Directory_name/
or you can provide a database of reference genomes with
--ref_db Database_dir/
You can use iva_qc_make_ref_db
to make a reference
database. See this page for help.
Do not clean temporary files
Number of threads to use when running SMALT. Default: 1.
Show program's version number and exit.
Minimum hit length when running nucmer of contigs against reference. Default: 100.
Minimum hit percent identity when running nucmer of contigs against reference. Default: 80.
Minimum hit length when running nucmer of CDS sequences against contigs. Default: 30.
Minimum hit percent identity when running nucmer of CDS sequences against contigs. Default: 80.
Minimum percent identity used when GAGE runs nucmer Default: 80.
Use the --preload
option when running kraken.
Only applies if --ref_db
is used.
Specify your own RATT config file, instead of the
one that is bundled with IVA. If you want to
find this file, read the description of
this option in your terminal when running this script
with --help
.
These options are used to change the mapping settings when the reads are mapped to each of the reference genome and assembly.
kmer hash length in SMALT (the -k option in smalt index). Default: 15.
kmer hash step size in SMALT (the -s option in smalt index). Default: 3.
Minimum identity threshold for mapping to be reported (the -y option in smalt map). Default: 0.5
Title to use in contig layout plot. Put it in quotes. Default: "IVA QC contig layout and read depth".
Minimum read coverage of the reference, on each strand, to count as OK coverage. Default: 5