Hi Dave,

Perhaps the bedItemOverlapCount utility in our source tree can help you 
obtain the visualization you are looking for. A pre-compiled version can 
be found here: http://hgdownload.cse.ucsc.edu/admin/exe (note we only 
have versions complied for linux and MacOSX). One of the arguments for 
this program is the chromosome sizes, which are typically accessed from 
a mysql database. To bypass this have your database be "none" (you do 
need to give it something for this argument) and then specify the 
-chromSize= to be a file containing the chrom sizes, which can be found 
here for mm9: http://hgdownload.cse.ucsc.edu/goldenPath/mm9/database/ 
chromInfo.txt.gz.

This will output a bedGraph file. If your data is genome-wide, you 
should then convert it to a bigWig using the bedGraphToBigWig utility, 
also available in the same location mentioned above.

I hope this information is helpful.  Please feel free to contact the 
mail list again if you require further assistance.

Best,
Mary
------------------
Mary Goldman
UCSC Bioinformatics Group

On 6/24/10 7:23 AM, David A. wrote:
> Dear list,
>
> I am trying to visualize alignment of my Illumina reads in the Genome 
> Browser. The result I am trying to get is a track where I can see the reads 
> piling up, as if they were peaks of alignment, as  is shown in many articles 
> and presentations. To do so, as I want to load alignment against the whole 
> mouse genome, I transformed my Illumina _sorted.txt to BED format and this 
> BED format to BigBed format so that transfering data to the Genome Browser 
> was faster. But I am getting just plain rectangular boxes at the given 
> positions of alignment and not a nice shaped peak that would allow me to 
> rougly compare peak heights visually.
>
> Where am I going wrong?
>
> Thanks for your help
>
> Dave
>                                       
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