illuminapairedend
: aligns paired-end Illumina reads¶
Important
illuminapairedend
replaces solexapairend
.
illuminapairedend
aims at aligning the two reads of a pair-end library sequenced
using an Illumina platform.
- If the two reads overlap, it returns the consensus sequence together with its quality
- Otherwise, it concatenates sequence merging the forward read and the reversed-complemented reverse read.
The program uses as input one or two fastq 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.
illuminapairedend
align the forward sequence record with the reverse complement of the
reverse sequence record. The alignment algorithm takes into account the base qualities.
Example:
> illuminapairedend -r seq3P.fastq seq5P.fastq > seq.fastqThe
seq5P.fastq
sequence file contains the forward sequence records. Theseq3P.fastq
sequence file contains the reverse sequence records. Pairs of reads are aligned together and the consensus sequence is stored in the `` seq.fastq`` file.
illuminapairedend
specific options¶
-
-r
<FILENAME>
,
--reverse-reads
=<FILENAME>
¶ Filename points to the file containing the reverse reads.
-
--score-min
=<FLOAT>
¶ minimum score for keeping alignment. If the alignment score is below this threshold both the sequences are just concatenated. The
mode
attribute is set to the valuejoined
.