bbabbd5d2566d47d923d51dbe350634783455999
mspeir
  Sun Oct 26 12:14:52 2025 -0700
change soe to gi, refs #35031

diff --git src/hg/htdocs/goldenPath/mapPlots/RHguide.html src/hg/htdocs/goldenPath/mapPlots/RHguide.html
index 3c359d7a732..d25f2a00b37 100644
--- src/hg/htdocs/goldenPath/mapPlots/RHguide.html
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  <font SIZE="4"><a NAME="TOC"></a><b>&nbsp; Users Guide for STS Maps vs. Genome Sequence Asembly Comparison Plots</font>
  </td></tr></table>
 
 <!--outer table is for border purposes--> <table BGCOLOR="fffee8"
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 WIDTH=10></td><td> 
 
 	The purpose of the STS Maps vs. Genome Sequence Assembly
 	scatter plots is to show the correspondence between previously
 	constructed genome-wide STS maps and the different clones
 	maps.  We show one plot for each chromosome that displays the
 	STS marker posistions for the Genethon, Marshfield, GeneMap99,
 	G3, TNG, Whitehead Integrated and Whitehead-YAC maps.  The
 	y-axis of the plots represent positions in the STS maps, while
 	the x-axis represents positions in the clone maps.  The
 	primary plots are scaled to fit an entire chromosome on one
 	page. Additional plots are available which show portions of
 	each chromosome in fixed scale 50mb windows and 10mb
 	windows.<P></P>
       
         Each STS marker is represented by a point that is colored and
         shape-coded as described in the legend in the upper right
         corner. The horizontal position of the point is the location
         of the marker on the clone map of the chromosome in
         megabases. The vertical position of the point is the distance
         of the marker along the chromosome as determined by one of the
         seven STS maps. All seven maps are scaled to have comparable
         distance ranges to facilitate comparison. Some markers map to
         different chromosomes entirely. These are shown at the top of
         the display.<P></P>
       
         As you mouse-over the graph, the contig you are in, as
         determined by your horizontal position, is displayed in the
         little window at the bottom of the browser. (Position of this
         is dependent on the browser and platform being used.) Clicking
         on a contig will bring up a corresponding Summary Page which
         is part of our <A HREF="http://genome.ucsc.edu/goldenPath/chromReports">
         Chromosome Reports</A> web pages.  This Summary Page displays
         information about that particular contig with links to more
         detailed information.<P></P>
 
       <B>Caveats:</B>
       <UL>
 	<LI>Due to the resolution, it is hard to pinpoint the clone
 	contig for some markers. Go to a higher resolution plot if it
 	appears that the marker you clicked on is not included in the
 	report you get.  
 	<LI>We use BLAT to place STS markers, but do
 	not require an exact match of the STS sequence and/or primer
 	sequences.  This will cause some false positive placements,
 	and some false negatives as well, mainly due to the draft
 	nature of the sequence.  
         <LI>We have not yet incorporated LOD
 	scores for the markers. 
 	<LI>There are limitations of the
 	accuracy of each of the seven maps, for more details see 
 	"<A HREF="http://www.nature.com/genomics/human/papers/409860a0_fs_1.html">Initial
 	sequencing and analysis of the human genome</A>," by the
 	International Human Genome Sequencing Consortium, Nature,
 	409:860-921.
       </UL>
       <hr>
 	<address><a href="mailto:booch@cse.ucsc.edu">Terry Furey</a></address>
 	<!-- Created: Fri Aug  3 13:14:49 PDT 2001 -->
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 Last modified: Fri Mar 22 13:48:36 PST 2002
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