MIRACONVERT(1)

NAME
miraconvert - convert assembly and sequencing file types

SYNOPSIS
miraconvert [-f <fromtype>] [-t <totype> [-t <totype> ...]] [-aAChimMsuZ] [-cflnNoPqrtvxXyYz {...}] {infile} {outfile} [<totype> <totype> ...]

OPTIONS

-f <fromtype>
    load this type of project files, where fromtype is:

    caf a complete assembly or single sequences from CAF

    maf a complete assembly or single sequences from CAF

    fasta sequences from a FASTA file

    fastq sequences from a FASTQ file

    gb[f|k|ff] sequences from a GenBank file

    phd sequences from a PHD file

    fofnexp sequences in EXP files from file of filenames

-t <totype>
    write the sequences/assembly to this type (multiple mentions of -t are allowed):

    ace sequences or complete assembly to ACE

    caf sequences or complete assembly to CAF

    maf sequences or complete assembly to MAF

    sam complete assembly to SAM

    samnbb like above, but leaving out reference (backbones) in mapping assemblies

    gb[f|k|ff] sequences or consensus to GenBank

    gff3 consensus to GFF3

    wig assembly coverage info to wiggle file

    gcwig assembly gc content info to wiggle file

    fasta sequences or consensus to FASTA file (qualities to .qual)

    fastq sequences or consensus to FASTQ file

    exp sequences or complete assembly to EXP files in directories. Complete assemblies are suited for gap4 import as directed assembly. Note: using caf2gap to import into gap4 is recommended though

    text complete assembly to text alignment (only when -f is caf, maf or gbf)

    html complete assembly to HTML (only when -f is caf, maf or gbf)

    tcs complete assembly to tcs

    hsnp surrounding of SNP tags (SROc, SAOc, SIOc) to HTML (only when -f is caf, maf or gbf)

    asnp analysis of SNP tags (only when -f is caf, maf or gbf)

    cstats contig statistics file like from MIRA (only when source contains contigs)

    crlist contig read list file like from MIRA (only when source contains contigs)

    maskedfasta reads where sequencing vector is masked out (with X) to FASTA file (qualities to .qual)

    scaf sequences or complete assembly to single sequences CAF

-a  Append to target files instead of rewriting

-A  Do not Adjust sequence case

    When reading formats which define clipping points, and saving to formats which do not have clipping information, miraconvert normally adjusts the case of read sequences: lower case for clipped parts, upper case for unclipped parts of reads. Use -A if you do not want this. See also -C.

    Applies only to files/formats which do not contain contigs.

-b  Blind data

    Replaces all bases in reads/contigs with a 'c'

-C  Perform hard clip to reads

    When reading formats which define clipping points, will save only the unclipped part into the result file.

    Applies only to files/formats which do not contain contigs.

-d  Delete gap only columns

    When output is contigs: delete columns that are entirely gaps (like after having deleted reads during editing in gap4 or similar)

    When output is reads: delete gaps in reads

-F  Filter read groups to different files

    Works only for input files with readgroups (CAF/MAF) 3 (or 4) files generated: one or two for paired, one for unpaired and one for debris reads.

    Reads in paired file are interlaced by default, use -F twice to create separate files.

-m  Make contigs (only for -t = caf or maf)

    Encase single reads as contig singlets into the CAF/MAF file.

-n <filename>
    when given, selects only reads or contigs given by name in that file.

-N <filename>
    like -n, but sorts output according to order given in file.

-i  when -n is used, inverts the selection

-o <quality>t
    FASTQ quality Offset (only for -f = 'fastq')

    Offset of quality values in FASTQ file. Default of 33 loads Sanger/Phred style files, using 0 tries to automatically recognise.

-P <string>
    String with MIRA parameters to be parsed

    Useful when setting parameters affecting consensus calling like -CO:mrpg etc.

    E.g.: -P "454_SETTINGS -CO:mrpg=3"

-q <quality>
    Set default quality for bases in file types without quality values. Furthermore, do not stop if expected quality files are missing (e.g. '.fasta')

-R <name>
    Rename contigs/singlets/reads with given name string to which a counter is appended.

    Known bug: will create duplicate names if input contains contigs/singlets as well as free reads, i.e. reads not in contigs nor singlets.

-S <name>
    (name)Scheme for renaming reads, important for paired-ends. Only 'solexa' is currently supported.

-T  When converting single reads, trim/clip away stretches of N and X and ends of reads. Note: remember to use -C to also perform a hard clip (e.g. with FASTA as output).

-v  Print version number and exit

-Y <integer>
    Yield. Max (clipped/padded) bases to convert.

    When used on reads: output will contain first reads of file where length of clipped bases totals at least -Y. When used on contigs: output will contain first contigs of file where length of padded contigs totals at least -Y.

The following switches work only when input (CAF or MAF) contains contigs. Beware: CAF and MAf can also contain just reads.

-M  Do not extract contigs (or their consensus), but the sequence of the reads they are composed of.

-r [cCqf]
    Recalculate consensus and / or consensus quality values and / or SNP feature tags.

    'c' recalc cons & cons qualities (with IUPAC)

    'C' recalc cons & cons qualities (forcing non-IUPAC)

    'q' recalc consensus qualities only

    'f' recalc SNP features

    Note: only the last of cCq is relevant, f works as a switch and can be combined with cQq (e.g. "-r C -r f")

    Note: if the CAF/MAF contains multiple strains, recalculation of cons & cons qualities is forced, you can just influence whether IUPACs are used or not.

-s  split output into multiple files instead of creating a single file

-u  'fillUp strain genomes'

    Fill holes in the genome of one strain (N or @) with sequence from a consensus of other strains

    Takes effect only with -r and -t gbf or fasta/q in FASTA/Q: bases filled up are in lower case in GBF: bases filled up are in upper case

-Q <integer>
    Defines minimum quality a consensus base of a strain must have, consensus bases below this will be 'N' Default: 0

    Only used with -r, and -f is caf/maf and -t is (fasta or gbf)

-V <integer>
    Defines minimum coverage a consensus base of a strain must have, bases with coverage below this will be 'N' Default: 0

    Only used with -r, and -t is (fasta or gbf)

-x <integer>
    Minimum contig or unclipped read length

    When loading, discard all contigs / reads with a length less than this value. Default: 0 (=switched off)

    Note: not applied to reads in contigs!

-X <integer>
    Similar to -x but applies only to reads and then to the clipped length.

-y <integer>
    Minimum average contig coverage When loading, discard all contigs with an average coverage less than this value. Default: 1

-z <integer>
    Minimum number of reads in contig When loading, discard all contigs with a number of reads less than this value. Default: 0 (=switched off)

-l <integer>
    when output as text or HTML: number of bases shown in one alignment line. Default: 60.

-c <character>
    when output as text or HTML: character used to pad endgaps. Default: ' ' (blank)

EXAMPLES

    miraconvert source.maf dest.sam

    miraconvert source.caf dest.fasta wig ace

    miraconvert -x 2000 -y 10 source.caf dest.caf

    miraconvert -x 40 -C -F -F source.maf .fastq

    miraconvert: Missing infile and out-basename as arguments!

AUTHOR
The program miraconvert was written by Bastien Chevreux <bach@chevreux.org>.

This manpage was written by Andreas Tille for the Debian distribution and can be used for any other usage of the program.