An ultra-fast all-in-one FASTQ preprocessor (QC/adapters/trimming/filtering/splitting/merging...)
MIT License
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Published by sfchen over 6 years ago
Published by sfchen over 6 years ago
Published by sfchen over 6 years ago
Published by sfchen over 6 years ago
Published by sfchen over 6 years ago
Published by sfchen almost 7 years ago
Published by sfchen almost 7 years ago
Published by sfchen almost 7 years ago
Published by sfchen almost 7 years ago
Published by sfchen almost 7 years ago
For Illumina NextSeq/NovaSeq data, polyG can happen in read tails since G means no signal in the Illumina two-color systems. fastp can detect the polyG in read tails and trim them. This feature is enabled for NextSeq/NovaSeq data by default, and you can specify -g or --trim_poly_g to enable it for any data, or specify -G or --disable_trim_poly_g to disable it. NextSeq/NovaSeq data is detected by the machine ID in the FASTQ records.
Published by sfchen almost 7 years ago
Published by sfchen almost 7 years ago
Published by sfchen almost 7 years ago
Published by sfchen almost 7 years ago
Published by sfchen almost 7 years ago
Published by sfchen almost 7 years ago
Published by sfchen almost 7 years ago
Published by sfchen almost 7 years ago
use -s <adapter_sequence> to enable trimming for single end data
Published by sfchen almost 7 years ago
Published by sfchen almost 7 years ago
The output can be split to multiple files for parallel processing