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Proper Citation: Human Splicing Finder (RRID:SCR_005181)
Description: Software tool to help study pre-mRNA splicing and to better understand intronic and exonic mutations leading to splicing defects. To calculate the consensus values of potential splice sites and search for branch points, new algorithms were developed. Furthermore, they have integrated all available matrices to identify exonic and intronic motifs, as well as new matrices to identify hnRNP A1, Tra2-? and 9G8.
Abbreviations: HSF
Resource Type: service resource, analysis service resource, production service resource, data analysis service
Defining Citation: PMID:19339519
Keywords: splicing, mutation, splicing signal, sequence, transcript, nucleotide, exon, bio.tools
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National Institute of Health and Medical Research; Rennes; France |
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Source: SciCrunch Registry
