fasta_nucleotide_changer
FASTQ/A short nucleotide reads pre-processing tools
Install
- All systems
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curl cmd.cat/fasta_nucleotide_changer.sh
- Debian
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apt-get install fastx-toolkit - Ubuntu
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apt-get install fastx-toolkit - Kali Linux
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apt-get install fastx-toolkit - Fedora
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dnf install fastx_toolkit - Windows (WSL2)
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sudo apt-get updatesudo apt-get install fastx-toolkit - Raspbian
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apt-get install fastx-toolkit - Dockerfile
- dockerfile.run/fasta_nucleotide_changer
fastx-toolkit
FASTQ/A short nucleotide reads pre-processing tools
The FASTX-Toolkit is a collection of command line tools for preprocessing short nucleotide reads in FASTA and FASTQ formats, usually produced by Next-Generation sequencing machines. The main processing of such FASTA/FASTQ files is mapping (aligning) the sequences to reference genomes or other databases using specialized programs like BWA, Bowtie and many others. However, it is sometimes more productive to preprocess the FASTA/FASTQ files before mapping the sequences to the genome—manipulating the sequences to produce better mapping results. The FASTX-Toolkit tools perform some of these preprocessing tasks.