Fig. 1From: SMURF-seq: efficient copy number profiling on long-read sequencersSMURF-seq efficiently sequences short fragments of DNA for read-counting applications with a reference genome on long-read sequencers and yields up to 30 countable fragments per sequenced read. SMURF-seq sequences short DNA molecules by generating long concatenated molecules from these. SMURF-seq reads are aligned by splitting them into multiple fragments, each aligning to a distinct region in the genomeBack to article page