Servizi per la Bioinformatica

GSNAP

GSNAP (Genomic Short-read Nucleotide Alignment Program) can align both single-end and paired-end reads as short as 14 nt and of arbitrarily long length. It can detect short- and long-distance splicing, including interchromosomal splicing, in individual reads using probabilistic models or a database of known splice sites.