Hello Zhang,

To obtain the actual data values, use output format = data points 
(instead of BED, which only provides positional information).

The new output will be in compressed wiggle format. A description of 
that format is here:
http://genome.ucsc.edu/goldenPath/help/wiggle.html

And if you would like the complete data per base (instead of the 
compressed summary), the files can be anonymously ftp'd from the 
downloads server here:
http://hgdownload.cse.ucsc.edu/downloads.html#human
scroll to the build (hg19, hg18, etc.) and look for the heading 
"Multiple Alignments" and the sub-link "Basewise conservation scores 
(phyloP) of 45 vertebrate genomes with Human"

For hg19, this would be:
http://hgdownload.cse.ucsc.edu/goldenPath/hg19/phyloP46way/
A description of the files and ftp/rsync help is in the README

To directly answer your question, no the data is not a complete 1-1 
exact match, these are probability scores. The Conservation track has 
help describing the process in the Methods section (click on the track 
name in the main Assembly viewer).

Hopefully this helps. Please feel free to contact the mailing list 
support team again if you would like more assistance.

Warm regards,

Jen
UCSC Genome Browser Support

On 9/1/10 9:18 AM, Zhang Wensheng wrote:
> Hello,
>
> I am a new UCSC Genome Browser user. I have a question about table "Mammal
> Cons(PhyloP44wayPlacMammal" in clad:Mammal and genome:Human. When the position
> information was specified via "define regions",
>
>
> chr1    869396    869824
> chr1    869445    869936
> chr1    890434    890958
> chr1    899818    900345
> chr1    924205    924301
>
> I got the the output file in BED format as following,
>
> track type=wiggle_0 name="tb_phyloP44wayPlacMammal" description="table browser
> query on phyloP44wayPlacMammal" visibility=2 url=
>
> chr1    869396    869824    chr1.1
> chr1    869445    869936    chr1.1
> chr1    890434    890958    chr1.1
> chr1    899818    900345    chr1.1
> chr1    924205    924301    chr1.1
>
>
> Could please help me by explaining this result? Specially, I want to know if 
> it
> means that, in the case of the first line, the sequence Human ch1:86939-869824
> can be perfectly aligned with a region of other genomes (one or all).
>
>
> Thanks you very much
>
>
>
>
> _______________________________________________
> Genome maillist  -  [email protected]
> https://lists.soe.ucsc.edu/mailman/listinfo/genome
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