fastQ_brew: module for analysis, preprocessing, and reformatting of FASTQ sequence data.

BMC Res Notes

Institute for Neuroscience, The George Washington University, 636 Ross Hall, 2300 I St. N.W., Washington, DC, 20052, USA.

Published: July 2017

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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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5508660PMC
http://dx.doi.org/10.1186/s13104-017-2616-7DOI Listing

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