55a7d0bdb8cb52deaf829c50d9b5db7c95018f79 jnavarr5 Mon Jul 29 08:40:19 2019 -0700 Updating http to https for monDom1, uiLinks cronjob. diff --git src/hg/makeDb/trackDb/opossum/multiz5way.html src/hg/makeDb/trackDb/opossum/multiz5way.html index 233d150..80d1c4c 100644 --- src/hg/makeDb/trackDb/opossum/multiz5way.html +++ src/hg/makeDb/trackDb/opossum/multiz5way.html @@ -1,169 +1,169 @@ <H2>Description</H2> <P> This track shows a measure of evolutionary conservation in $organism, chicken, human, mouse, and zebrafish, based on a phylogenetic hidden Markov model (phastCons). Multiz alignments of the following assemblies were used to generate this annotation: <UL> <LI>opossum Jun. 2005 (monDom2) <LI>chicken Feb. 2004 (galGal2) <LI>human May 2004 (hg17) <LI>mouse May 2004 (mm5) <LI>zebrafish June 2004 (danRer2)</UL></P> <P> In full display mode, this track shows the overall conservation score across all species as well as pairwise alignments of each species aligned to the $organism genome. The pairwise alignments are shown in dense display mode using a grayscale density gradient. The checkboxes in the track configuration section allow the exclusion of species from the pairwise display; however, this does not remove them from the conservation score display. </P> <P> When zoomed-in to the base-display level, the track shows the base composition of each alignment. The numbers and symbols on the Gaps line indicate the lengths of gaps in the $organism sequence at those alignment positions relative to the longest non-$organism sequence. If there is sufficient space in the display, the size of the gap is shown; if not, and if the gap size is a multiple of 3, a "*" is displayed, otherwise "+" is shown. To view detailed information about the alignments at a specific position, zoom in the display to 30,000 or fewer bases, then click on the alignment.</P> <P> This track may be configured in a variety of ways to highlight different aspects of the displayed information. Click the <A HREF="../goldenPath/help/hgWiggleTrackHelp.html" TARGET=_blank>Graph configuration help</A> link for an explanation of the configuration options.</P> <H2>Methods</H2> <P> Best-in-genome blastz pairwise alignments were multiply aligned using multiz, beginning with $organism-chicken alignments and subsequently adding in human, mouse, and zebrafish. The resulting multiple alignments were then assigned conservation scores by phastCons.</P> <P> The phastCons program computes conservation scores based on a 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 (Felsenstein and Churchill 1996, Yang 1995, Siepel and Haussler 2005). PhastCons uses a two-state phylo-HMM, with a state for conserved regions and a state for non-conserved regions. The value plotted at each site is the posterior probability that the corresponding alignment column was "generated" by the conserved state of the phylo-HMM. These scores reflect the phylogeny (including branch lengths) of the species in question, a continuous-time Markov model of the nucleotide substitution process, and a tendency for conservation levels to be autocorrelated along the genome (i.e., to be similar at adjacent sites). The general reversible (REV) substitution model was used. Note that, unlike many conservation-scoring programs, phastCons does not rely on a sliding window of fixed size, so short highly-conserved regions and long moderately conserved regions can both obtain high scores. More information about phastCons can be found in Siepel et al. (2005).</P> <P> PhastCons currently treats alignment gaps as missing data, which sometimes has the effect of producing undesirably high conservation scores in gappy regions of the alignment. We are looking at several possible ways of improving the handling of alignment gaps.</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/miller_lab/" 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. <LI>"Wiggle track" plotting software by Hiram Clawson at UCSC. </UL> </P> <P>The phylogenetic tree is based on Murphy et al. (2001) and general consensus in the vertebrate phylogeny community. </P> <H2>References</H2> <H3>Phylo-HMMs and phastCons:</H3> <P> Felsenstein J, Churchill GA. <A HREF="https://academic.oup.com/mbe/article/13/1/93/1055515" TARGET=_blank>A Hidden Markov Model approach to variation among sites in rate of evolution</A>. <em>Mol Biol Evol</em>. 1996 Jan;13(1):93-104. PMID: <a href="https://www.ncbi.nlm.nih.gov/pubmed/8583911" target="_blank">8583911</a> </p> <P> Siepel A, Haussler D. <A HREF="http://compgen.cshl.edu/~acs/phylohmm.pdf" TARGET=_blank>Phylogenetic Hidden Markov Models</A>. In: Nielsen R, editor. Statistical Methods in Molecular Evolution. New York: Springer; 2005. pp. 325-351. </P> <P> Siepel A, Bejerano G, Pedersen JS, Hinrichs AS, Hou M, Rosenbloom K, Clawson H, Spieth J, Hillier LW, Richards S, <EM>et al.</EM> <A HREF="https://genome.cshlp.org/content/15/8/1034" TARGET=_blank>Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes</A>. <em>Genome Res</em>. 2005 Aug;15(8):1034-50. PMID: <a href="https://www.ncbi.nlm.nih.gov/pubmed/16024819" target="_blank">16024819</a>; PMC: <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1182216/" target="_blank">PMC1182216</a> </p> <P> Yang Z. -<A HREF="http://www.genetics.org/content/139/2/993" +<A HREF="https://www.genetics.org/content/139/2/993" TARGET=_blank>A space-time process model for the evolution of DNA sequences</A>. <em>Genetics</em>. 1995 Feb;139(2):993-1005. PMID: <a href="https://www.ncbi.nlm.nih.gov/pubmed/7713447" target="_blank">7713447</a>; PMC: <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1206396/" target="_blank">PMC1206396</a> </p> <H3>Chain/Net:</H3> <P> Kent WJ, Baertsch R, Hinrichs A, Miller W, Haussler D. <A HREF="https://www.pnas.org/content/100/20/11484" TARGET=_blank>Evolution's cauldron: duplication, deletion, and rearrangement in the mouse and human genomes</A>. <em>Proc Natl Acad Sci U S A</em>. 2003 Sep 30;100(20):11484-9. PMID: <a href="https://www.ncbi.nlm.nih.gov/pubmed/14500911" target="_blank">14500911</a>; PMC: <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC208784/" target="_blank">PMC208784</a> </p> <H3>Multiz:</H3> <P> Blanchette M, Kent WJ, Riemer C, Elnitski L, Smit AF, Roskin KM, Baertsch R, Rosenbloom K, Clawson H, Green ED, <EM>et al.</EM> <A HREF="https://genome.cshlp.org/content/14/4/708.abstract" TARGET=_blank>Aligning multiple genomic sequences with the threaded blockset aligner</A>. <em>Genome Res</em>. 2004 Apr;14(4):708-15. PMID: <a href="https://www.ncbi.nlm.nih.gov/pubmed/15060014" target="_blank">15060014</a>; PMC: <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC383317/" target="_blank">PMC383317</a> </p> <H3>Blastz:</H3> <P> Chiaromonte F, Yap VB, Miller W. <A HREF="http://psb.stanford.edu/psb-online/proceedings/psb02/chiaromonte.pdf" TARGET=_blank>Scoring pairwise genomic sequence alignments</A>. <EM>Pac Symp Biocomput</EM>. 2002:115-26. PMID: <a href="https://www.ncbi.nlm.nih.gov/pubmed/11928468" target="_blank">11928468</a> </P> <H3>Phylogenetic Tree:</H3> <P> Murphy WJ, Eizirik E, O'Brien SJ, Madsen O, Scally M, Douady CJ, Teeling E, Ryder OA, Stanhope MJ, de Jong WW, Springer MS. -<A HREF="http://science.sciencemag.org/content/294/5550/2348" +<A HREF="https://science.sciencemag.org/content/294/5550/2348" TARGET=_blank>Resolution of the early placental mammal radiation using Bayesian phylogenetics</A>. <EM>Science</EM>. 2001 Dec 14;294(5550):2348-51. PMID: <a href="https://www.ncbi.nlm.nih.gov/pubmed/11743200" target="_blank">11743200</a> </P>