RobersonLab/paired_end_demux
Illumina FASTQ files as input and splits into individual indexed samples.
Public GitHub Catalog
Discovered Sep 28, 2026
RobersonLab / compare_order
Compare the read ids between two Illumina FASTQ or SCARF files to confirm reads are in sync.
About this discovery
This repository is cataloged as part of our automated global GitHub synchronization. Full telemetry, velocity snapshots, and code summaries are scheduled for continuous enrichment.
#12710614GitHub System ID
RobersonLabOrganization / User
PublicVisibility
ActiveCatalog Status
More from RobersonLab
RobersonLab/single_end_demux
Python script for demultiplexing single-end sequencing into individual FASTQ files by index.
RobersonLab/RobersonLab.github.io
Lab static site
RobersonLab/fastq_scrubber
Really hacky way to remove adapters from NGS while keeping reads in order. Recommend alt strategy with cutadapt instead.