RobersonLab/paired_end_demux
Illumina FASTQ files as input and splits into individual indexed samples.
Discovered public repositories for RobersonLab in the GitHub catalog.
Illumina FASTQ files as input and splits into individual indexed samples.
Python script for demultiplexing single-end sequencing into individual FASTQ files by index.
Lab static site
Really hacky way to remove adapters from NGS while keeping reads in order. Recommend alt strategy with cutadapt instead.
Compare the read ids between two Illumina FASTQ or SCARF files to confirm reads are in sync.
C++ method to convert ILMN+64 files between SCARF and FASTQ formats.
Simple program that converts FASTQ files in Solexa quality offset (QUAL+64) to a FASTQ file with Phred/Sanger offset (QUAL+33).
Functions that allow direct differential expression testing of 1 versus 1 array using the average intensities, bead count, standard errors and detection p-values. Requires beadarray.
Repository for the web-based version / visualization engine for the SNPduoWeb tool. Designed to visualize identity-by-state in high-density snp data. Originally developed in the lab of Dr. Jonathan Pevsner. The newest versions are Roberson Lab adaptations.
Repository for the snpduo command-line tool. The tool is designed to calculate identity-by-state in large SNP genotyping datasets. Originally developed in the lab of Dr. Jonathan Pevsner at the Kennedy Krieger Institute in Baltimore. Publication PMID: 19696932.