Hello,

In the description of this track it states:

"To be considered spliced, an EST must show evidence of at least one 
canonical intron, i.e. the genomic sequence between EST alignment blocks 
must be at least 32 bases in length and have GT/AG ends."

BLAT is used to generate the alignments and it starts a new block 
whenever there is an indel. So you can end up with a PSL that looks like 
it has two adjacent blocks in the genome sequence because there is an 
insertion in the mRNA (i.e. a deletion in the genome sequence).

Thus there can be additional gaps in the alignments (in addition to the 
minimum 'one canonical intron') due to indels. Often sequencing error or 
polymorphism can cause indels.

Hopefully this information was helpful and answers your question. If you 
have further questions or require clarification feel free to contact the 
mailing list at [email protected].

Regards,

Pauline Fujita
UCSC Genome Bioinformatics Group
http://genome.ucsc.edu

On 04/06/11 08:38, HE Liu,Student wrote:
> hi guys:
> 
> this is probably a really stupid question, but it do confuse me...
> 
> based on the description of SpilcedEST track:
> the genomic sequence between EST alignment
> blocks must be at least 32 bases in length and have GT/AG ends.
> and by a simply checking, i find that substantial proportion of distances 
> between 2 neighboring alignment blocks of an EST sequence is less or equal 
> than 1, doesn't this mean these 2 neighboring blocks are actually continuous 
> region? if they are, why would them be 2 blocks?
> by the description, it sounds like alignment blocks are exons... or i 
> misunderstand these blocks are just produced by Blat, and i need to check 
> canonical GT/AT sites from genome sequence in order to get right exon-intron 
> structures?
> 
> Thanks~~
> 
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