src/hg/makeDb/trackDb/phastConsElements.html 1.22

1.22 2009/06/26 01:03:53 pauline
Added italics.
Index: src/hg/makeDb/trackDb/phastConsElements.html
===================================================================
RCS file: /projects/compbio/cvsroot/kent/src/hg/makeDb/trackDb/phastConsElements.html,v
retrieving revision 1.21
retrieving revision 1.22
diff -b -B -U 1000000 -r1.21 -r1.22
--- src/hg/makeDb/trackDb/phastConsElements.html	15 Sep 2006 20:58:06 -0000	1.21
+++ src/hg/makeDb/trackDb/phastConsElements.html	26 Jun 2009 01:03:53 -0000	1.22
@@ -1,96 +1,96 @@
 <H2>Description</H2> 
 <P> 
 This track shows predictions of conserved elements produced by the phastCons
 program.  PhastCons is part of the PHAST (PHylogenetic Analysis with 
 Space/Time models) package.  The predictions are based on a phylogenetic hidden 
 Markov model (phylo-HMM), a type of probabilistic model that describes both 
 the process of DNA substitution at each site in a genome and the way this 
 process changes from one site to the next. </P>
 
 <H2>Methods</H2>
 <P>
 Best-in-genome pairwise alignments were generated for
 each species using blastz, followed by chaining and netting.  A multiple
 alignment was then constructed from these pairwise alignments using multiz.
 Predictions of conserved elements were then obtained by running phastCons
 on the multiple alignments with the --most-conserved option.</P>
 <P>
 PhastCons constructs a two-state phylo-HMM with a state for conserved
 regions and a state for non-conserved regions.  The two states share a
 single phylogenetic model, except that the branch lengths of the tree
 associated with the conserved state are multiplied by a constant scaling
 factor <em>rho</em> (0 <= <em>rho</em> <= 1).  The free parameters of the
 phylo-HMM, including the scaling factor <em>rho</em>, are estimated from
 the data by maximum likelihood using an EM algorithm.  This procedure is
 subject to certain constraints on the "coverage" of the genome by conserved
 elements and the "smoothness" of the conservation scores.  Details can be
-found in Siepel et al. (2005).</P>
+found in Siepel <em>et al</em>. (2005).</P>
 <P>
 The predicted conserved elements are segments of the alignment that are
 likely to have been "generated" by the conserved state of the phylo-HMM.
 Each element is assigned a log-odds score equal to its log probability
 under the conserved model minus its log probability under the non-conserved
 model.  The "score" field associated with this track contains transformed
 log-odds scores, taking values between 0 and 1000.  (The scores are
 transformed using a monotonic function of the form a * log(x) + b.)  The
 raw log odds scores are retained in the "name" field and can be seen on the
 details page or in the browser when the track's display mode is set to
 "pack" or "full".</P>
 
 <H2>Credits</H2>
 <P>
 This track was created at UCSC using the following programs:
 <UL>
 <LI>
 Blastz and multiz by Minmei Hou, Scott Schwartz and Webb Miller of the 
 <A HREF="http://www.bx.psu.edu/" TARGET=_blank>Penn State Bioinformatics 
 Group</A>. 
 <LI>
 AxtBest, axtChain, chainNet, netSyntenic, and netClass
 by Jim Kent at UCSC. 
 <LI>PhastCons by Adam Siepel at Cornell University. 
 </UL>
 </P>
 
 <H2>References</H2>
 
 <H3>PhastCons</H3>
 <P>
 Siepel, A., Bejerano, G., Pedersen, J.S., Hinrichs, A., Hou, M., Rosenbloom, 
 K., Clawson, H., Spieth, J., Hillier, L.W., Richards, S., Weinstock, G.M., 
 Wilson, R. K., Gibbs, R.A., Kent, W.J., Miller, W., and Haussler, D. 
 <A HREF="http://www.genome.org/cgi/doi/10.1101/gr.3715005"
 TARGET=_blank>Evolutionarily conserved elements in vertebrate, insect, worm, 
 and yeast genomes</A>.
 <em>Genome Res.</em> <B>15</B>, 1034-1050 (2005).</P>
 
 <H3>Chain/Net</H3>
 <P>
 Kent, W.J., Baertsch, R., Hinrichs, A., Miller, W., and Haussler, D.
 <A HREF="http://www.pnas.org/cgi/content/abstract/1932072100v1" 
 TARGET=_blank>Evolution's cauldron: Duplication, deletion, and rearrangement
 in the mouse and human genomes</A>.
 <em>Proc Natl Acad Sci USA</em> <B>100</B>(20), 11484-11489 (2003).</P>
 
 <H3>Multiz</H3>
 <P>
 Blanchette, M., Kent, W.J., Riemer, C., Elnitski, L., Smit, A.F.A., 
 Roskin, K.M., Baertsch, R., Rosenbloom, K., Clawson, H., Green, E.D., 
 Haussler, D., Miller, W. 
 <A HREF="http://www.genome.org/cgi/content/abstract/14/4/708" 
 TARGET=_blank>Aligning multiple genomic sequences with the threaded blockset
 aligner</A>.
 <em>Genome Res.</em> <B>14</B>(4), 708-15 (2004).</P>
 
 <H3>Blastz</H3>
 <P>
 Chiaromonte, F., Yap, V.B., Miller, W. 
 <A HREF="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=11928468&dopt=Abstract" 
 TARGET=_blank>Scoring pairwise genomic sequence alignments</A>. 
 <em>Pac Symp Biocomput 2002</em>, 115-26 (2002).</P>
 <P>
 Schwartz, S., Kent, W.J., Smit, A., Zhang, Z., Baertsch, R., Hardison, R., 
 Haussler, D., and Miller, W.
 <A HREF="http://www.genome.org/cgi/content/abstract/13/1/103" 
 TARGET=_blank>Human-Mouse Alignments with BLASTZ</A>. 
 <em>Genome Res.</em> <B>13</B>(1), 103-7 (2003).</P>