Adapter_Trimming

Basic Usage

The Adapter_Trimming handler trims adapters off samples. This script utilizes Scythe on paired-end or single-end data. To run Adapter_Trimming, all common and wrapper-specific variables must be defined within the configuration file. Once the variables have been defined, Adapter_Trimming can be submitted to a job scheduler with the following command:

sequence_handling Adapter_Trimming Config

Where Config is the full file path to the configuration file.

Variables

The following are a list of variables that need to be defined within Config. In addition to the handler-specific variables, all common variables must be defined.

Variable	Function
AT_QSUB	QSub settings for batch submission. Recommended settings are "mem=1gb,nodes=1:ppn=8,walltime=10:00:00".
FORWARD_NAMING	Naming convention for forward reads. If your files are named sample1_R1.fastq and sample2_R1.fastq, FORWARD_NAMING=_R1.fastq
REVERSE_NAMING	Naming convention for reverse reads. If your files are named sample1_R2.fastq and sample2_R2.fastq, FORWARD_NAMING=_R2.fastq
ADAPTERS	A plain text or FastA file with the adapter sequences.
PRIOR	A prior value for Scythe. The recommended value is 0.05.

Output

Adapter_Trimming creates trimmed FastQ files for each sample. In addition, a list of all trimmed files will be output for use with other handlers. The full file path to this list will be

${OUT_DIR}/Adapter_Trimming/${PROJECT}_things.txt

where ${OUT_DIR} and ${PROJECT} are specified in the configuration file.

After running Adapter_Trimming, there are three options for further processing.

1. Quality_Assessment can be used for more complete quality assurance.
2. Quality_Trimming can be used to trim low quality bases.
3. Read_Mapping can be used to map reads to a reference genome.

Dependencies

Adapter_Trimming depends on Scythe to perform the trimming. This is not installed on MSI and must be installed separately. Furthermore, PBS and GNU Parallel are required for basic running.

Next: Quality_Trimming or Read_Mapping