Open Eduardo-Alves opened 7 years ago
More on the use of Gnomon here. Broadly it looks like the Compart tool is used to convert BLAST hits into regions to examine and Splign / ProSplign are used in a manner similar to exonerate to refine alignments. There is much to wrap besides these tools, but as a start, these tools are part of the NCBI C++ toolkit. Compiling the entire toolkit is a large job. The build system would have to be used to only build the necessary components.
I have installed the whole NCBI C++ toolkit on my Linux System, but I cannot find 'gnonom' in the bin directory. And I found no tutorial about Gnomon on the NCBI website... I also tried to contact NCBI, but no response. Anyone knows how to use Gnomon? Thanks!
I was trying the NCBI Eukaryotic genome annotation pipeline but was unable to find any maual or tutorial for Gnomon. Can anyone guide me how to use it.
Thanks
NCBI pipeline for eukaryotic annotation uses gnomon: "Protein, transcript and RNA-Seq read alignments are passed to Gnomon for gene prediction. Gnomon first chains together non-conflicting alignments into putative models. In a second step, Gnomon extends predictions missing a start or a stop codon or internal exon(s) using an HMM-based algorithm. Gnomon additionally creates pure ab initio predictions where open reading frames of sufficient length but with no supporting alignment are detected." https://www.ncbi.nlm.nih.gov/genome/annotation_euk/process/
There are no license restrictions and the code is part of ncbi toolkit: "NCBI C++ Toolkit provides free, portable, public domain libraries with no restrictions use" https://www.ncbi.nlm.nih.gov/IEB/ToolBox/CPP_DOC/ https://www.ncbi.nlm.nih.gov/viewvc/v1/trunk/c%2B%2B/src/algo/gnomon/