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Updated: Jun 12, 2025

Detection of Rare Genomic Variants from Pooled Sequencing Using SPLINTER
Published on: June 23, 2012
Scalable and unsupervised discovery from raw sequencing reads using SPLASH2
Marek Kokot1, Roozbeh Dehghannasiri2,3, Tavor Baharav4,5,6
1Department of Algorithmics and Software, Silesian University of Technology, Gliwice, Poland.
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We introduce SPLASH2, a fast, scalable implementation of SPLASH based on an efficient k-mer counting approach for regulated sequence variation detection in massive datasets from a wide range of sequencing technologies and biological contexts. We demonstrate biological discovery by SPLASH2 in single-cell RNA sequencing (RNA-seq) data and in bulk RNA-seq data from the Cancer Cell Line Encyclopedia, including unannotated alternative splicing in cancer transcriptomes and sensitive detection of circular RNA.

