IntSplice 1.1 – Prediction of the Splicing Consequences of Intronic Single-nucleotide Variations in the Human Genome

IntSplice 1.1

:: DESCRIPTION

IntSplice is a tool to predict a splicing consequence of an SNV at intron positions -50 to -3 close the 3’ end of an intron of the human genome.

::DEVELOPER

IntSplice team

:: SCREENSHOTS

N/A

:: REQUIREMENTS

  • Web browser

:: DOWNLOAD

 NO

:: MORE INFORMATION

Citation

IntSplice: prediction of the splicing consequences of intronic single-nucleotide variations in the human genome.
Shibata A, Okuno T, Rahman MA, Azuma Y, Takeda JI, Masuda A, Selcen D, Engel AG, Ohno K.
J Hum Genet. 2016 Mar 24. doi: 10.1038/jhg.2016.23.