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fastQ_brew: module for analysis, preprocessing, and reformatting of FASTQ sequence data
BACKGROUND: Next generation sequencing datasets are stored as FASTQ formatted files. In order to avoid downstream artefacts, it is critical to implement a robust preprocessing protocol of the FASTQ sequence in order to determine the integrity and quality of the data. RESULTS: Here I describe fastQ_b...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5508660/ https://www.ncbi.nlm.nih.gov/pubmed/28701181 http://dx.doi.org/10.1186/s13104-017-2616-7 |
Sumario: | BACKGROUND: Next generation sequencing datasets are stored as FASTQ formatted files. In order to avoid downstream artefacts, it is critical to implement a robust preprocessing protocol of the FASTQ sequence in order to determine the integrity and quality of the data. RESULTS: Here I describe fastQ_brew which is a package that provides a suite of methods to evaluate sequence data in FASTQ format and efficiently implements a variety of manipulations to filter sequence data by size, quality and/or sequence. fastQ_brew allows for mismatch searches to adapter sequences, left and right end trimming, removal of duplicate reads, as well as reads containing non-designated bases. fastQ_brew also returns summary statistics on the unfiltered and filtered FASTQ data, and offers FASTQ to FASTA conversion as well as FASTQ reverse complement and DNA to RNA manipulations. CONCLUSIONS: fastQ_brew is open source and freely available to all users at the following webpage: https://github.com/dohalloran/fastQ_brew. |
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