Dear UCSC team, Hiram,

> With these MAF files, a bed file of your specific regions and the kent
program mafsInRegion

Where can I get source or binary for mafsInRegion?

I think I found it's source in the UCSC genome browser source (
http://hgdownload.cse.ucsc.edu/admin/jksrc.zip)? But according to
README.building.source I would have to build the entire thing locally? It's
a bit tough... (steps 3a - 5 are a bit complex, and I cannot / don't want
to build mySQL on the intended target machine).

Is there a more direct way to get the source for mafsInRegion and compile
only this one?

Thanks.
Anton


On Fri, Jul 20, 2012 at 3:01 PM, Hiram Clawson <[email protected]> wrote:

> Good Evening Anton:
>
> You can fetch a beta release set of MAF files for a 60-species alignment
> on Mouse/GRCm38/mm10 from our test server:
>
> http://hgdownload-test.cse.**ucsc.edu/goldenPath/mm10/**multiz60way/maf/<http://hgdownload-test.cse.ucsc.edu/goldenPath/mm10/multiz60way/maf/>
>
> Or the 46 species alignment MAF files from Human/GRCh37/hg19:
> http://hgdownload.cse.ucsc.**edu/goldenPath/hg19/**multiz46way/maf/<http://hgdownload.cse.ucsc.edu/goldenPath/hg19/multiz46way/maf/>
>
> Beware, these are gigantic files.  With these MAF files, a bed file
> of your specific regions and the kent program mafsInRegion, you can
> obtain the sequence out of these files.  It is not perfectly in multi Fasta
> format, but it is close enough for a simple transformation.
>
> --Hiram
>
>  mafsInRegion - Extract MAFS in a genomic region
>> usage:
>>     mafsInRegion regions.bed out.maf|outDir in.maf(s)
>> options:
>>     -outDir - output separate files named by bed name field to outDir
>>     -keepInitialGaps - keep alignment columns at the beginning and of a
>>                        block that are gapped in all species
>>
>
> On 7/19/12 10:07 PM, Anton Kratz wrote:
>
>> Dear UCSC team,
>>
>> I have a list of a couple of thousand exons or regions on the rat (rn4)
>> genome defined as start-end coordinates in bed format. These regions are
>> not in RefSeq, RGD or elsewhere, they are novel determined by me. I want
>> to
>> check for coding/noncoding poteintial with phyloCSF (
>> https://github.com/mlin/**PhyloCSF/wiki/<https://github.com/mlin/PhyloCSF/wiki/>
>> ).
>>
>> Is there any way how I programmatically can get multi-genome alignment for
>> my regions, in FASTA-format? Ideally for the 29 mammals phylogeny but any
>> other multi-alignment containing mammals is fine too.
>>
>> I was searching around in the data at UCSC provided in context of the 29
>> mammals 
>> (http://genomewiki.cse.ucsc.**edu/index.php/29mammals<http://genomewiki.cse.ucsc.edu/index.php/29mammals>)
>> project, but
>> can't find the actual multi-fasta alignment.
>>
>> Thanks.
>>
>> Anton
>> ______________________________**_________________
>> Genome maillist  -  [email protected]
>> https://lists.soe.ucsc.edu/**mailman/listinfo/genome<https://lists.soe.ucsc.edu/mailman/listinfo/genome>
>>
>
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