roryk/breakseq2
BreakSeq2: Ultrafast and accurate nucleotide-resolution analysis of structural variants
DEPRECATED Lightweight bioinformatics pipeline tools using iPython
This repository is cataloged as part of our automated global GitHub synchronization. Full telemetry, velocity snapshots, and code summaries are scheduled for continuous enrichment.
BreakSeq2: Ultrafast and accurate nucleotide-resolution analysis of structural variants
My datasets - Original data or Aggregated / cleaned / restructured existing datasets. Released here under Creative Commons B
Classify A->I RNA editing events from RNA-seq variants
Windowed Adaptive Trimming for fastq files using quality