Actually is rewrite based on the lite version

for dumping out a test region

Some bugs with BaseAlign still there.

to avoid loading all of (e.g. dna table) into memory

Now does two different mapping, one for the prediction and one for the known genes... it will allow us to be more free to tickle the parameters

Added a specific option in the mapping_conf file for NCBI prediction. Flaged the different entries retrieved in get_Xmapping.pl; KNOWN for SPTR and curated Refseq, XREF for all of the entries retrieved from the KNOWN matches and then PRED for all of the sequences predicted by other teams (in that case NCBI for human but can be anything).

some tables missing, not yet best area of genome.

them into Fpc tables. Missing: Accessions for the clones.

hopefully useful for comeing schema conversions.

moved sub's to bottom to make it readable