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To rememdy this, we feel that some modifications can be made:
- Eucaryotes
- Don Fong and David Haussler have looked at ways to use multiple
states. A publication should be forthcoming describing the
equations which are necessary to do this.
- False +
- For elimination of false positives, we think that
analyzing contigs for G/C content and modifying the gene codon usage
tables might be successful [6]. Another way to
eliminate false positives could be to strengthen the translational
initiation sensor by studying the -35 regions as well as the -10
region.
- tRNA & mRNA
- For recognition of tRNA and rRNA genes, their sequences could be
analyzed statistically to see if their recognition is compatible
with mRNA genes. It may be that we only need to build a length
histogram and codon usage table from a training dataset of all three
types of genes, and weaken the start and stop codon sensors (tRNA
and rRNA genes don't have the same start and stop codons as mRNA
genes)
David Konerding
Sun May 21 12:19:38 PDT 1995