Hello Jim,

The program that we use to convert the original PSL alignment files 
(http://genome.ucsc.edu/FAQ/FAQformat.html#format2) for RefSeq Genes to 
GenePred format (http://genome.ucsc.edu/FAQ/FAQformat.html#format9) 
merges blocks that are less than 8 bp apart.  We have added the task of 
better documenting this to our to-do list.

However, if you really need to look at indels, you should look at the 
actual alignments instead of the genePred tables created from the 
alignments.  Even if the gaps were not closed, as in the case you have 
pointed out, the genePred format can't represent insertions in the mRNA, 
since it's a genome annotation.  The alignments are in the refSeqAli table.

If you have further questions, please contact us again at 
[email protected].

--
Brooke Rhead
UCSC Genome Bioinformatics Group



Jim Robinson wrote on 11/19/11 8:50 PM:
>    Hi,
>
> I think there is an error in the annotation for NEFL on hg19 in the
> refGene.txt.gz download.   Specifically, it is missing a 1 base
> insertion (intron) at position 24,811,071.  I think the correct record
> should be
>
> 774    NM_006158    chr8    -    24808468    24814131    24810322
> 24814029    5    24808468,24810988,24811071,24811694,24812985,
> 24810465,24811070,24811309,24811819,24814131,    0    NEFL    cmpl
> cmpl    1,0,2,0,0
>
> best,
>
> Jim
>
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