obijoinpairedend - description of obijoinpairedend
obijoinpairedend aims at joining the two reads of a
paired-end library.
For this purpose, it concatenates sequence merging the forward
read and the reversed-complemented reverse read.
The program uses as input one or two sequences reads files.
- If two files are used one of them must be specified using the -r
option. Sequence records corresponding to the same read pair must be in
the same order in the two files.
- If just one file is provided, sequence records are supposed to be all of
the same length. The first half of the sequence is used as forward read,
the second half is used as the reverse read.
Example:
> obijoinpairedend -r seq3P.fastq seq5P.fastq > seq.fastq
The seq5P.fastq sequence file contains the forward sequence
records. The seq3P.fastq sequence file contains the reverse sequence
records. Pairs of reads are joined together and the resulting sequence is
stored in the `` seq.fastq`` file.
- --skip
<N>
- The N first sequence records of the file are discarded from the analysis
and not reported to the output file
- --only
<N>
- Only the N next sequence records of the file are analyzed. The following
sequences in the file are neither analyzed, neither reported to the output
file. This option can be used conjointly with the –skip
option.
- --embl
- Input file is in embl format.
- --fasta
- Input file is in fasta format (including OBITools fasta extensions).
- --sanger
- Input file is in Sanger fastq format (standard fastq used by HiSeq/MiSeq
sequencers).
- --solexa
- Input file is in fastq format produced by Solexa (Ga IIx) sequencers.
- --ecopcr
- Input file is in ecoPCR format.
- --nuc
- Input file contains nucleic sequences.
- --prot
- Input file contains protein sequences.
- --fasta-output
- Output sequences in OBITools fasta format
- --ecopcrdb-output=<PREFIX_FILENAME>
- Creates an ecoPCR database from sequence records results
- --uppercase
- Print sequences in upper case (default is lower case)
- --DEBUG
- Sets logging in debug mode.
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