Different version of fasta dump (SEE BELOW)


Will try vanilla dump first.

purplepelican:sratoolkit.2.1.6-mac32 srlab$ ./fastq-dump -A SRR327417 /Volumes/Bay4/OysterGenomeBGI/SRX089200/SRR327417/SRR327417.sra -O /Volumes/Bay4/Oyster_SRAconverts  


purplepelican:sratoolkit.2.1.6-mac32 srlab$ ./fastq-dump -A SRR327417 /Volumes/Bay4/OysterGenomeBGI/SRX089200/SRR327417/SRR327417.sra -O /Volumes/Bay4/Oyster_SRAconverts 
Written 55031989 spots for /Volumes/Bay4/OysterGenomeBGI/SRX089200/SRR327417/SRR327417.sra
Written 55031989 spots total


and splitting into 2 files

purplepelican:sratoolkit.2.1.6-mac32 srlab$ ./fastq-dump -A SRR327417 /Volumes/Bay4/OysterGenomeBGI/SRX089200/SRR327417/SRR327417.sra --split-files -O /Volumes/Bay4/scratchy 


Processing OysterBGI fosmids



ERROR



purplepelican:sratoolkit.2.1.6-mac32 srlab$ ./fastq-dump -helpUsage:
  ./fastq-dump [options] [ -A ] <accession>
  ./fastq-dump [options] <path[ path...]>

INPUT
  -A|--accession <accession>       Replaces accession derived from <path> in
                                   filename(s) and deflines (only for single
                                   table dump)
  --table <table-name>             [NEW] Table name within cSRA object,
                                   default is "SEQUENCE"

PROCESSING

Read Splitting                     Sequence data may be used in raw form or
                                     split into individual reads
  --split-spot                     Split spots into individual reads

Full Spot Filters                  Applied to the full spot independently
                                     of --split-spot
  -N|--minSpotId <rowid>           Minimum spot id
  -X|--maxSpotId <rowid>           Maximum spot id
  --spot-groups <[list]>           Filter by SPOT_GROUP (member): name[,...]
  -W|--clip                        Apply left and right clips

Common Filters                     Applied to spots when --split-spot is not
                                     set, otherwise - to individual reads
  -M|--minReadLen <len>            Filter by sequence length >= <len>
  -R|--read-filter <[filter]>      Split into files by READ_FILTER value
                                   optionally filter by value:
                                   pass|reject|criteria|redacted
  -E|--qual-filter                 Filter used in early 1000 Genomes data: no
                                   sequences starting or ending with >= 10N

Filters based on alignments        Filters are active when alignment
                                     data are present
  --aligned                        Dump only aligned sequences
  --unaligned                      Dump only unaligned sequences
  --aligned-region <name[:from-to]>  Filter by position on genome. Name can
                                   either be accession.version (ex:
                                   NC_000001.10) or file specific name (ex:
                                   "chr1" or "1"). "from" and "to" are 1-based
                                   coordinates
  --matepair-distance <from-to|unknown>  Filter by distance beiween matepairs.
                                   Use "unknown" to find matepairs split
                                   between the references. Use from-to to limit
                                   matepair distance on the same reference

Filters for individual reads       Applied only with --split-spot set
  --skip-technical                 Dump only biological reads

OUTPUT
  -O|--outdir <path>               Output directory, default is working
                                   directory '.' )
  -Z|--stdout                      Output to stdout, all split data become
                                   joined into single stream

Multiple File Options              Setting these options will produce more
                                     than 1 file, each of which will be suffixed
                                     according to splitting criteria.
  --split-files                    Dump each read into separate file.Files
                                   will receive suffix corresponding to read
                                   number
  --split-3                        Legacy 3-file splitting for mate-pairs:
                                   First biological reads satisfying dumping
                                   conditions are placed in files *_1.fastq and
                                   *_2.fastq If only one biological read is
                                   present it is placed in *.fastq Biological
                                   reads and above are ignored.
  -G|--spot-group                  Split into files by SPOT_GROUP (member name)
  -R|--read-filter <[filter]>      Split into files by READ_FILTER value
                                   optionally filter by value:
                                   pass|reject|criteria|redacted
  -T|--group-in-dirs               Split into subdirectories instead of files
  -K|--keep-empty-files            Do not delete empty files

FORMATTING

Sequence
  -C|--dumpcs <[cskey]>            Formats sequence using color space (default
                                   for SOLiD),"cskey" may be specified for
                                   translation
  -B|--dumpbase                    Formats sequence using base space (default
                                   for other than SOLiD).

Quality
  -Q|--offset <integer>            Offset to use for quality conversion,
                                   default is 33
  --fasta                          FASTA only, no qualities

Defline
  -F|--origfmt                     Defline contains only original sequence name
  -I|--readids                     Append read id after spot id as
                                   'accession.spot.readid' on defline
  --helicos                        Helicos style defline
  --defline-seq <fmt>              Defline format specification for sequence.
  --defline-qual <fmt>             Defline format specification for quailty.
                                   <fmt> is string of characters and/or
                                   variables. The variables can be one of: $ac
                                   - accession, $si spot id, $sn spot
                                   name, $sg spot group (barcode), $sl spot
                                   length in bases, $ri read number, $rn
                                   read name, $rl read length in bases. '[]'
                                   could be used for an optional output: if
                                   all vars in [] yield empty values whole
                                   group is not printed. Empty value is empty
                                   string or for numeric variables. Ex:
                                   @$sn[_$rn]/$ri '_$rn' is omitted if name
                                   is empty
 
OTHER:
  -h|--help                        Output brief explanation of program usage
  -V|--version                     Display the version of the program
  -L|--log-level <level>           Logging level as number or enum string One
                                   of (fatal|sys|int|err|warn|info) or (0-5)
                                   Current/default is warn
  -v|--verbose                     Increase the verbosity level of the program
                                   Use multiple times for more verbosity

./fastq-dump : 2.1.6