Hi Ann,

Sorry for the delayed response. We suggest you try contacting the mailing list 
(http://reproductivegenomics.jax.org/mailing_list.html) at the Jackson 
Laboratory to see if you can obtain the sequences and positions from for the 
DMit microsatellite markers.

Once you have those, go to the main page on our site. Click on "Tables" from 
the blue navigation bar to get to our table browser.

Set the clade, genome, and assembly.

Set the following:

track: "UCSC Genes" 
table: "knownGene"
region: "position" and click on "define regions." Paste your regions in the box 
and click "submit"
output format: "all fields from selected table"

click "get output"

The result is the record for your gene. The exon/intron boundaries can be 
deduced from the exonStarts and exonEnds fields. If there are many fields in 
the record that you don't need, you can hit the back button and change the 
output format to "selected fields from primary and related tables." Click "get 
output" and select the fields you wish to see in your results, be sure to 
include exonStarts and exonEnds since these fields contain the data you asked 
about.

Also, you may be interested in UCSC In-Silico PCR for mapping PCR products. To 
get to it, click on "PCR" from the blue navigation bar.

Hope this helps! If you have further questions related to the Genome Browser, 
please contact the mailing list.

Vanessa Kirkup Swing
UCSC Genome Bioinformatics Group

----- Original Message -----
From: "Ann Eileen Miller Baker" <[email protected]>
To: [email protected]
Sent: Wednesday, March 16, 2011 7:53:57 PM
Subject: [Genome] pls reply to [email protected]

pls reply to [email protected] because I am unclear how to access the
normal channel where replies are put

(1) How can I find mouse DMit (microsatellite loci) amplified sequences?
(url)
(2) alleles at inbred strains for DMit microsatellite loci? (url)
(3) How can I find which DMit microsatellite loci are in
- introns
- exons
- recombination hot spots
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