Constructs a new set of piped tasks for taking PE Illumina data from two fastq files and producing an unampped BAM file in which the possible location of adapter sequence in each read is marked.
Constructs a new set of piped tasks for taking PE Illumina data from two fastq files and producing an unampped BAM file in which the possible location of adapter sequence in each read is marked.
the read one fastq file (can be gzipped)
the read two fastq file (can be gzipped)
the output SAM or BAM file to write to
the name of the sample to put in the read group header
the name of the library to put in the read group header
the platform unit string to put in the tread group header
the optional ID to use in the read group header. If None one will be generated.
the prefix (including directories) to use to write metrics and ancillary files
a Pipe from Nothing (since the inputs are read from file) to SamOrBam