RobersonLab/paired_end_demux
Illumina FASTQ files as input and splits into individual indexed samples.
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Discovered Sep 27, 2026
RobersonLab / fastqSol2Phred
Simple program that converts FASTQ files in Solexa quality offset (QUAL+64) to a FASTQ file with Phred/Sanger offset (QUAL+33).
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RobersonLab/single_end_demux
Python script for demultiplexing single-end sequencing into individual FASTQ files by index.
RobersonLab/RobersonLab.github.io
Lab static site
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