3ed505903284ad261bd78055097acfb1db417f45
dschmelt
  Tue Jul 9 15:23:04 2019 -0700
Making links relative #23514

diff --git src/hg/htdocs/goldenPath/newsarch.html src/hg/htdocs/goldenPath/newsarch.html
index 9174cd1..f02527c 100755
--- src/hg/htdocs/goldenPath/newsarch.html
+++ src/hg/htdocs/goldenPath/newsarch.html
@@ -70,31 +70,31 @@
 creating, developing, and releasing this data track.</p> 
 
 <a name="070119"></a>
 <h2>Jul. 1, 2019 &nbsp;&nbsp; New DGV Gold Standard track for human (GRCh19/hg19)</h2>
 <p>
 We are pleased to announce the DGV Gold Standard track for human (GRCh19/hg19). This track displays
 copy number variants (CNVs), insertions/deletions (InDels), inversions and inversion breakpoints
 annotated by the <a href="http://dgv.tcag.ca/dgv/app/home" target="_blank">Database of Genomic Variants</a>
 (DGV). The initial criteria for the Gold Standard set require that a variant be found in at least
 two different studies and found in at least two different samples. After filtering out low-quality
 variants, the remaining variants are clustered according to 50% minimum overlap, and then merged
 into a single record. Gains and losses are merged separately.
 </p>
 
 <p>
-The <a href="https://genome.ucsc.edu/cgi-bin/hgTrackUi?db=hg19&g=dgvPlus" target="_blank">DGV Gold Standard track</a>
+The <a href="../cgi-bin/hgTrackUi?db=hg19&g=dgvPlus" target="_blank">DGV Gold Standard track</a>
 utilizes a boxplot-like display to represent the merging of records. The highest ranking variant in
 the cluster defines the inner &quot;box&quot;, while the outer lines define the outermost start and stop
 coordinates of the CNV. In this way, the inner box forms a high-confidence CNV location and the
 thin connecting lines indicate confidence intervals for the location of the CNV.
 </p>
 <p class="text-center">
   <img class='text-center' src="../images/dgvGold.png" width='850' alt="DGV Gold Standard track">
 </p>
 
 <p>
 We would like to thank Jeff MacDonald and the <a href="http://dgv.tcag.ca/dgv/app/home" target="_blank">Database of Genomic Variants</a>
 group for providing guidance and these data. We would also like to thank Christopher Lee and Conner
 Powell as well as the entire UCSC Genome Browser team for creating and releasing this track.
 </p>
 
@@ -3022,31 +3022,31 @@
 <h2>Aug. 30, 2016 &nbsp;&nbsp; Allele-specific expression in 53 tissues from GTEx Analysis Hub now
 available</h2>
 <p>
 We are pleased to announce the release of Allele Specific Expression (ASE) data for the human hg19 
 and hg38 assemblies. ASE data from the <a href="http://tllab.org" target="_blank">Lappalainen 
 Lab</a> at the New York Genome Center is now available in the UCSC Genome Browser as a public track 
 hub.  This track hub contains ASE data identified from transcriptome and genotype
 data in 53 tissues collected by the <a href="https://commonfund.nih.gov/GTEx/index" 
 target="blank">Genotype-Tissue Expression (GTEx) project</a> and analyzed by the Lappalainen Lab. 
 The hub contains 3 tracks, a cross tissue summary via density graph of median allelic imbalance, 
 a summary track of all SNPs with evidence of ASE in any tissue, and a composite track showing ASE 
 on a tissue by tissue basis. In the composite track each subtrack is colored based on median ASE for
 the site across all samples of the tissue, shaded on a spectrum of gray (low) to GTEx convention
 tissue color (high).</p>
 <p>
-To access and view this hub, navigate to the <a href="http://genome.ucsc.edu/cgi-bin/hgHubConnect" 
+To access and view this hub, navigate to the <a href="../cgi-bin/hgHubConnect" 
 target="_blank">Track Hub gateway page</a> and select &quot;GTEx Analysis Hub&quot; from the
 Public Hubs list. Please direct any queries to <a href="mailto:scastel@nygenome.org">Stephane 
 Castel</a>.</p>
 <p>
 Many thanks to Stephane Castel and the Lappalainen Lab at the NY Genome Center for providing this 
 data.</p>
 
 <a name="081616"></a>
 <h2>Aug. 16, 2016 &nbsp;&nbsp; dbSNP 147 available for hg19 and hg38</h2>
 <p>
 We are pleased to announce the release of four tracks derived from NCBI 
 <a href="https://www.ncbi.nlm.nih.gov/SNP/"> dbSNP</a> Build 147 data, available on the two most 
 recent human assemblies GRCh37/hg19 and GRCh38/hg38. NCBI's dbSNP database is a collection of 
 &quot;simple nucleotide polymorphisms&quot; (SNPs), which are a class of genetic variations
 that include single nucleotide polymorphisms and small insertions/deletions (indels). This immense 
@@ -3130,31 +3130,31 @@
 <ul>
   <li>
   193,647 transcripts did not change.</li>
   <li>
   128 transcripts were not carried forward to the new version.</li>
   <li>
   997 transcripts are "compatible" with those in the previous set, meaning that the two transcripts 
   show consistent splicing. In most cases, the old and new transcripts differ in the lengths of 
   their UTRs.</li>
   <li>
   406 transcripts overlap with those in the previous set, but do not show consistent splicing (i.e.,
   they contain overlapping introns with differing splice sites)</li>
 </ul>
 <p>
 More details about the GENCODE Genes track can be found on the
-<a href="http://genome.ucsc.edu/cgi-bin/hgTrackUi?db=hg38&g=knownGene">
+<a href="../cgi-bin/hgTrackUi?db=hg38&g=knownGene">
 GENCODE v24 track description page</a>.</p>
 <p>
 Many thanks to Brian Raney and Luvina Guruvadoo for their work on this track!</p>
 <hr>
 <p>
 We are  pleased to announce the release of an updated UCSC Genes track for the Mouse (GRCm38/mm10) 
 assembly. The new release has 63,759 total transcripts, compared with 63,244 in the previous 
 version. The total number of canonical genes has increased from 32,958 to 33,079. Comparing the new 
 gene set with the previous version:</p>
 <ul>
   <li>
   60,827 transcripts did not change between versions.</li>
   <li>
   148 transcripts were not carried forward to the new version.</li>
   <li>
@@ -3887,31 +3887,31 @@
 <ul>
   <li>
   9,459 transcripts did not change.</li>
   <li>
   22,088 transcripts were not carried forward to the new version.</li>
   <li>
   43,681 transcripts are "compatible" with those in the previous set, meaning that the two 
   transcripts show consistent splicing. In most cases, the old and new transcripts differ in the 
   lengths of their UTRs.</li>
   <li>
   28,950 transcripts overlap with those in the previous set, but do not show consistent splicing 
   (i.e., they contain overlapping introns with differing splice sites)</li>
 </ul>
 <p>
 More details about the new GENCODE Basic track can be found on the
-<a href="http://genome.ucsc.edu/cgi-bin/hgTrackUi?db=hg38&g=knownGene">
+<a href="../cgi-bin/hgTrackUi?db=hg38&g=knownGene">
 GENCODE Basic track description page</a>.</p>
 
 <a name="062615"></a>
 <h2>Jun. 26, 2015 &nbsp;&nbsp; New bonobo (panPan1) assembly now available in the Genome
 Browser</h2>
 <p>
 We are pleased to announce the release of a Genome Browser for the May 2012 assembly of bonobo, 
 <em>Pan paniscus</em> (Max-Planck Institute panpan1, UCSC version panPan1). The assembly was 
 provided by the <a href="http://www.eva.mpg.de/" target="_blank">Max-Planck Institute for 
 Evolutionary Anthropology</a>. There are 10,867 scaffolds with a total size of 2,869,190,071 
 bases.</p>
 <p>
 Bulk downloads of the sequence and annotation data are available via the Genome Browser
 <a href="ftp://hgdownload.soe.ucsc.edu/goldenPath/panPan1/">FTP server</a> or the
 <a href="http://hgdownload.soe.ucsc.edu/downloads.html#bonobo">Downloads</a> page. These data have
@@ -4249,42 +4249,42 @@
 <!-- above address is ucscgbtraining at soe.ucsc.edu -->
         
 <a name="011515"></a>
 <h2>Jan. 15, 2015 &nbsp;&nbsp; Proteomics data now available in Genome Browser</h2>
 <p>
 We are pleased to announce the release of proteomics data for the human hg19 assembly. Data from the
 National Cancer Institute's (NCI) <a href="http://proteomics.cancer.gov/programs/cptacnetwork" 
 target="_blank">Clinical Proteomic Tumor Analysis Consortium (CPTAC)</a> is now available in the 
 UCSC Genome Browser as a public track hub. This track hub contains peptides that were identified by 
 CPTAC in their deep mass spectrometry based characterization of the proteome content of breast, 
 colorectal and ovarian cancer biospecimens that were initially sequenced by 
 <a href="http://cancergenome.nih.gov/" target="_blank">The Cancer Genome Atlas</a>. This effort 
 extends the accessibility of CPTAC data to more researchers and provides an additional level of 
 analysis to assist the cancer biology community.</p>
 <p>
-To access and view this hub, navigate to the <a href="http://genome.ucsc.edu/cgi-bin/hgHubConnect" 
+To access and view this hub, navigate to the <a href="../cgi-bin/hgHubConnect" 
 target="_blank">Track Hub gateway page</a> and select &quot;CPTAC Hub v1&quot; from the Public Hubs 
 list.  Please direct any queries to the Fenyo Lab at 
 <a href="mailto:info@fenyolab.org">info@fenyolab.org</a>.</p>
 <p>
 In addition, we have also released a <a href="http://www.peptideatlas.org/" 
 target="_blank">PeptideAtlas</a> track which displays peptide identifications from the
 <a href="https://db.systemsbiology.net/sbeams/cgi/PeptideAtlas/buildDetails?atlas_build_id=433" 
 target="_blank">PeptideAtlas August 2014 (Build 433) Human build</a>. This build, based on 971 
 samples containing more than 420 million spectra, identified over a million distinct peptides 
 covering more than 15,000 canonical proteins. To read more about this track, please see the 
-<a href="http://genome.ucsc.edu/cgi-bin/hgTrackUi?db=hg19&g=peptideAtlas" 
+<a href="../cgi-bin/hgTrackUi?db=hg19&g=peptideAtlas" 
 target="_blank">track description page</a>. Many thanks to Eric Deutsch, Zhi Sun, and the 
 PeptideAtlas team at the Institute for Systems Biology, Seattle for providing this data.</p>
 
 <!-- ============= 2014 archived news ============= -->
 <a name="2014"></a>
 <a name="121914"></a>
 <h2>Dec. 19, 2014 &nbsp;&nbsp; New cow (bosTau8) assembly now available in the Genome Browser</h2>
 <p> 
 We are pleased to announce the release of a Genome Browser for the June 2014 assembly
 of cow, <i>Bos taurus</i> (Bos_taurus_UMD 3.1.1, UCSC version bosTau8). This updated cow 
 assembly was provided by the  <a href="http://www.cbcb.umd.edu/"
 target="_blank">UMD Center for Bioinformatics and Computational Biology</a> (CBCB). This assembly is
 an update to the previous UMD 3.1 (bosTau6) assembly.  UMD 3.1 contained 138 unlocalized contigs 
 that were found to be contaminants.  These have been suppressed in UMD 3.1.1.</p>
 <p>
@@ -4602,31 +4602,31 @@
 version on hg19. The total number of canonical genes has increased from 31,848 to 48,424. Comparing 
 the new gene set with the previous version:</p>
 <ul>
   <li>
   69,691 transcripts did not change between versions.</li>
   <li>
   619 transcripts were not carried forward to the new version.</li>
   <li>
   8,879 transcripts are "compatible" with those in the previous set, meaning that the two 
   transcripts show consistent splicing.</li>
   <li>
   3,393 transcripts overlap with those in the previous set.</li>
 </ul>
 <p>
 More details about the new UCSC Genes track can be found on the
-<a href="http://genome.ucsc.edu/cgi-bin/hgTrackUi?db=hg38&g=knownGene" 
+<a href="../cgi-bin/hgTrackUi?db=hg38&g=knownGene" 
 >UCSC Genes track description page</a>.</p>
 <p>
 Many thanks to Brian Raney, Jim Kent, and Luvina Guruvadoo for their work on this track.</p>
 
 <a name="050914"></a>
 <h2>May 9, 2014 &nbsp;&nbsp; Three new assemblies now available in the Genome Browser</h2>
 <p>
 A Genome Browser is now available for the Chinese hamster (<em>Cricetulus griseus</em>) assembly 
 released July 2013 by the <a href="http://www.genomics.cn/en/index" target="_blank">Beijing Genomics
 Institution-Shenzhen</a> (BGI version C_griseus_v1.0, UCSC version criGri1). For more information 
 and statistics about this assembly, see the NCBI assembly record for 
 <a href="https://www.ncbi.nlm.nih.gov/assembly/40911" target="_blank">C_griseus_v1.0</a>. There are 
 52,711 scaffolds with a total size of 2,360,146,428 bases.</p>
 <p>
 Bulk downloads of the sequence and annotation data may be obtained from the Genome Browser
@@ -4721,43 +4721,43 @@
   <li>
   We tracked down the cause of some unusual gaps in the alignments to a bug in the multiz program 
   used in our alignment pipeline. The Penn State Bioinformatics Group provided us with a fixed 
   version of multiz that we used to rerun the pipeline. </li>
   <li>
   We inadvertently used the pre-release assembly for one of the species in the 100-way alignment: 
   the panda. We replaced this assembly with the correct version and verified that the data sets for 
   all other species were correct before rerunning the pipeline.</li>
 </ol>
 
 <a name="041814"></a>
 <h2>Apr. 18, 2014 &nbsp;&nbsp; New motif displays for transcription factor ChIP-seq track and new 
 genome segmentations from ENCODE</h2>
 <p>
 The Browser's default displayed Transcription Factor ChIP-seq track is updating to the
-<a href="http://genome.ucsc.edu/cgi-bin/hgTrackUi?db=hg19&g=wgEncodeRegTfbsClusteredV3">latest data 
+<a href="../cgi-bin/hgTrackUi?db=hg19&g=wgEncodeRegTfbsClusteredV3">latest data 
 release</a>, which has been enhanced with the display of Factorbook motifs. Within a cluster, a 
 green highlight indicates the highest scoring site of a Factorbook-identified canonical motif for 
 the corresponding factor. Upon clicking a transcription factor's cluster with a motif, the 
 details page now displays the motif's sequence logo, alignment and underlying Positional 
 Weight Matrix. Also, the track configuration page now enables the filtering of factors.</p>
 <p>
 The newly added 
-<a href="http://genome.ucsc.edu/cgi-bin/hgTrackUi?db=hg19&g=wgEncodeAwgSegmentation">
+<a href="../cgi-bin/hgTrackUi?db=hg19&g=wgEncodeAwgSegmentation">
 Genome Segmentations from ENCODE</a> tracks display multivariate genome-segmentation performed on
-<a target=ucscVocab href="http://genome.ucsc.edu/cgi-bin/hgEncodeVocab?term=GM12878,H1-hESC,K562,HeLa-S3,HepG2,HUVEC">six human cell types</a>
+<a target=ucscVocab href="../cgi-bin/hgEncodeVocab?term=GM12878,H1-hESC,K562,HeLa-S3,HepG2,HUVEC">six human cell types</a>
 (GM12878, K562, H1-hESC, HeLa-S3, HepG2, and HUVEC), integrating ChIP-seq data for
-<a target=ucscVocab href="http://genome.ucsc.edu/cgi-bin/hgEncodeVocab?term=CTCF,H3K4me1,H3K4me2,H3K4me3,H3K27ac,H3K9ac,H3K36me3,H4K20me1,H3K27me3,Pol2,Input">
+<a target=ucscVocab href="../cgi-bin/hgEncodeVocab?term=CTCF,H3K4me1,H3K4me2,H3K4me3,H3K27ac,H3K9ac,H3K36me3,H4K20me1,H3K27me3,Pol2,Input">
 eight chromatin marks, RNA Polymerase II, the CTCF transcription factor and input data</a>. 
 In total, twenty-five states were used to segment the genome, and these states were then grouped and
 colored to highlight predicted functional elements. These Genome Segmentations are the same data as
 found in the Analysis Working Group Hub, but are now hosted natively in the Browser with 
 enhanced filtering capability where desired segmented states can be selected using the
 Filter by Segment Type' control on the track configuration page.</p>
 
 <a name="041514"></a>
 <h2>Apr. 15, 2014 &nbsp;&nbsp; New minke whale (balAcu1) assembly now available</h2>
 <p>
 A Genome Browser is now available for the minke whale (Balaenoptera acutorostrata scammoni)
 assembly released October 2013 by the <a href="http://eng.kiost.ac/kordi_eng/main/" target="_BLANK">
 Korea Ocean Research &amp; Development Institute</a> (KORDI version BalAcu1.0, UCSC version 
 balAcu1). For more information and statistics about this assembly, see the NCBI assembly record for
 <a href="https://www.ncbi.nlm.nih.gov/assembly/78761" target="_blank">BalAcu1.0</a>. There are
@@ -4920,77 +4920,77 @@
 cover other costs.</p>
 <p>
 For more information or to submit a request for a workshop, please visit
 <a href="http://bit.ly/ucscTraining" target="_blank">our signup</a>.</p>
 
 <a name="012214"></a>
 <h2>Jan. 22, 2014 &nbsp;&nbsp; All the DNA on the internet now at your fingertips</h2>
 <p>
 We're pleased to announce the release of the Web Sequences track on the UCSC Genome Browser.
 This track, produced in collaboration with Microsoft Research, contains the results of a 30-day 
 scan for DNA sequences from over 40 billion different webpages. The sequences were then mapped with 
 Blat to the human genome (hg19) and numerous other species including mouse (mm9), rat (rn4), and 
 zebrafish (danRer7). The data were extracted from a variety of sources including patents, online 
 textbooks, help forums, and any other webpages that contain DNA sequence. In essence, this track 
 displays the Blat alignments of nearly every DNA sequence on the internet! The
-<a href="http://genome.ucsc.edu/cgi-bin/hgTrackUi?db=hg19&g=pubsBingBlat">Web Sequences</a>
+<a href="../cgi-bin/hgTrackUi?db=hg19&g=pubsBingBlat">Web Sequences</a>
 track description page contains more details on how the track was generated.</p>
 <p>
 We would like to acknowledge Max Haeussler and Matt Speir from the UCSC Genome Browser staff
 and Bob Davidson from Microsoft Research for their hard work in creating this track.</p>
 
 <a name="011414"></a>
 <h2>Jan. 14, 2014 &nbsp;&nbsp; Two E. coli comparative assembly hubs now available</h2>
 <p>
 We're pleased to add two new assembly hubs produced by the UCSC
 <a href="https://ucscgenomics.soe.ucsc.edu/team/" target="_blank">David Haussler lab</a> to our
 collection of publicly available hubs. The new hubs feature over 60 bacterial assemblies,
 including more than 55 different E. coli strains. The assembly annotations include genes, 
 pathogenic genes, conservation, GC percent, repetitive elements and much more.</p>
 <p>
 These hubs focus on comparative genomics and showcase the new &quot;snake&quot; track type. Snakes, 
 which visualize alignments from
 <a href="http://genome.ucsc.edu/FAQ/FAQformat.html#format20">Hierarchical Alignment</a>
 (HAL) files, provide a way to view sets of pairwise gapless alignments that may overlap on 
 both the chosen genome (reference) and the query genome, and show various types of genomic 
 variations such as insertions, substitutions, and duplications. More details about the new snake 
 track display and its configuration options can be found on our Genome Browser
 <a href="http://genome.ucsc.edu/goldenPath/help/hgTracksHelp.html" 
 target="_blank">help</a> page.</p>
 <p>
 To access and view these hubs, navigate to the
-<a href="http://genome.ucsc.edu/cgi-bin/hgHubConnect">Track Hub gateway page</a>
+<a href="../cgi-bin/hgHubConnect">Track Hub gateway page</a>
 and select one of the two E. coli comparative assembly hubs from the Public Hubs list.</p>
 <p>
 We would like to acknowledge Ngan Nguyen, Glenn Hickey, Brian Raney, Joel Armstrong, 
 Benedict Paten, Matt Speir, and Luvina Guruvadoo for their hard work in creating these hubs.</p>
 
 <!-- ============= 2013 archived news ============= -->
 
 <a name="2013"></a>
 <a name="112713"></a>
 <h2>Nov. 27, 2013 &nbsp;&nbsp; 100-Species Conservation track now available on hg19</h2>
 <p>
 After 15.4 years of CPU run-time in 9,905,594 individual jobs and 99 cluster runs for lastz
 pair-wise alignment...we are excited to announce the release of a 100 species alignment on 
 the hg19/GRCh37 human Genome Browser.</p>
 <p>
 This new Conservation track shows multiple alignments of 100 species and measurements of
 evolutionary conservation using two methods (phastCons and phyloP) from the PHAST package.
 This adds 40 more species to the existing 60-way on the mm10 mouse browser. For more information 
 about the 100 species Conservation track, see its 
-<a href="http://genome.ucsc.edu/cgi-bin/hgTrackUi?db=hg19&g=cons100way" 
+<a href="../cgi-bin/hgTrackUi?db=hg19&g=cons100way" 
 target="_blank">description page</a>.</p>
 <p>
 We'd also like to acknowledge the hard work of the UCSC Genome Browser staff who pulled 
 together the information for this track: Hiram Clawson and Pauline Fujita.</p>
 
 <a name="102413"></a>
 <h2>Oct. 24, 2013 &nbsp;&nbsp; Job opening: UCSC Genome Browser Trainer</h2>
 <p>
 The <a href="http://cbse.ucsc.edu/" target="_blank">Center for Biomolecular Science
 and Engineering</a> (CBSE) at UCSC seeks an articulate, self-motivated educator for the two-year 
 position of UCSC Genome Browser trainer. The trainer develops curriculum and provides in-person 
 training on the UCSC Genome Browser at universities, hospitals, institutes, and professional
 meetings in the United States and internationally. Typical audiences include graduate 
 and post-graduate biologists and doctors, with Genome Browser experience ranging from novice
 users to bioinformatics specialists. Presentations include formal talks, problem-solving 
@@ -5225,31 +5225,31 @@
 <ul>
   <li>
   74,657 transcripts did not change between versions.</li>
   <li>
   88 transcripts were not carried forward to the new version.</li>
   <li>
   5,556 transcripts are "compatible" with those in the previous set, meaning that the two 
   transcripts show consistent splicing. In most cases, the old and new transcripts differ in the 
   lengths of their UTRs.</li>
   <li>
   621 transcripts overlap with those in the previous set but do not show consistent splicing, 
   i.e., they contain overlapping introns with differing splice sites.</li>
 </ul>
 <p>
 More details about the new UCSC Genes track can be found on the 
-<a href="http://genome.ucsc.edu/cgi-bin/hgTrackUi?db=hg19&g=knownGene" >UCSC Genes track description
+<a href="../cgi-bin/hgTrackUi?db=hg19&g=knownGene" >UCSC Genes track description
 page</a>.</p>
 <p>
 Many thanks to Brian Raney, Jim Kent, and Luvina Guruvadoo for their work on this track.</p>
 
 <a name="062713"></a> 
 <h2>Jun. 27, 2013 &nbsp;&nbsp; New supported European mirror site established</h2>
 <p>
 The UCSC Genome Browser is pleased to announce the introduction of a new mirror site to serve our 
 users in Europe. Genome-euro is an official European mirror site of the UCSC Genome Browser at 
 <a href="http://genome-euro.ucsc.edu" target="_blank">http://genome-euro.ucsc.edu</a>. The server 
 is physically located at the Universit&auml;t Bielefeld Center for Biotechnology in Bielefeld, 
 Germany, and is administered by UCSC. Genome-euro is meant to be an alternate, faster access point 
 for those Browser users who are geographically closer to central Europe than to the western United 
 States.</p>
 <p>