FACIL infers the genetic code directly from any set of nucleic acid sequences and assigns a Random Forest-based reliability score to its predictions. To run FACIL, start by entering a genome sequence or a set of sequence fragments derived from the same genome into the search box below. It is important that the sequences are derived from the same genome to prevent mixing signals from potentially conflicting genetic codes. For example, a eukaryotic cell may contain up to three different translation codes: nuclear, mitochondrial and plastid.
:: MORE INFORMATION
BE Dutilh et al. (2011),
“FACIL: fast and accurate genetic code inference and logo“,
Bioinformatics 27: 1929.