Caution
This is a modified version of the 1.2 release. Made for use with the MGnify pipeline.
SeqPrep is a bioinformatics tool primarily used for processing paired-end Illumina reads. It excels in merging overlapping reads and trimming adapter sequences, making it a valuable asset in genomic sequence analysis. Its efficient handling of paired-end data ensures high-quality preparation for downstream analysis.
- Read Merging: Seamlessly merges overlapping paired-end Illumina reads into longer, single reads.
- Adapter Trimming: Efficiently trims adapter sequences from read ends to improve data quality.
- Quality Control: Offers options for quality score cutoff and minimum read length, enhancing the integrity of output data.
For a detailed tutorial on how to use SeqPrep, please refer to the SeqPrep Tutorial.