8c2f7318d8d821de9b2a25750586a94ab5e8c1bb
lrnassar
  Fri Nov 15 18:50:19 2024 -0800
Giving the UI link cronjob some love by fixing all the 301 redirects. These are the bulk of the items listed on the cron. No RM.

diff --git src/hg/makeDb/trackDb/tetraodon/chainSelf.html src/hg/makeDb/trackDb/tetraodon/chainSelf.html
index f5115e3..e25ff24 100644
--- src/hg/makeDb/trackDb/tetraodon/chainSelf.html
+++ src/hg/makeDb/trackDb/tetraodon/chainSelf.html
@@ -1,96 +1,96 @@
 <H2>Description</H2>
 <P>
 This track shows alignments of the $Organism genome with itself, using
 a gap scoring system that allows longer gaps than traditional
 affine gap scoring systems. The system can also tolerate gaps
 in both sets of sequence simultaneously.  After filtering out the 
 &quot;trivial&quot; alignments produced when identical locations of the 
 genome map to one another (e.g. chr<em>N</em> mapping to chr<em>N</em>), 
 the remaining alignments point out areas of duplication within the 
 $Organism genome. </P>
 <P>
 The chain track displays boxes joined together by either single or
 double lines. The boxes represent aligning regions.  Single lines indicate 
 gaps that are largely due to a deletion in the query assembly or an 
 insertion in the target assembly.  Double lines represent more complex gaps 
 that involve substantial sequence in both the query and target assemblies. 
 This may result from inversions, overlapping deletions, an abundance of local 
 mutation, or an unsequenced gap in one of the assemblies. In cases where 
 multiple chains align over a particular region of the $Organism genome, the 
 chains with single-lined gaps are often due to processed pseudogenes, while 
 chains with double-lined gaps are more often due to paralogs and unprocessed 
 pseudogenes. </P>
 <P>
 In the "pack" and "full" display
 modes, the individual feature names indicate the chromosome, strand, and
 location (in thousands) of the match for each matching alignment.</P>
 
 
 <H2>Display Conventions and Configuration</H2>
 <P>By default, the chains to chromosome-based assemblies are colored
 based on which chromosome they map to in the aligning organism. To turn
 off the coloring, check the &quot;off&quot; button next to: Color
 track based on chromosome.</P>
 <P>
 To display only the chains of one chromosome in the aligning
 organism, enter the name of that chromosome (e.g. chr4) in box next to: 
 Filter by chromosome.</P>
 
 <H2>Methods</H2>
 <P>
 The genome was aligned to itself using blastz. Trivial alignments were 
 filtered out, and the remaining alignments were converted into axt format
 using the lavToAxt program. The axt alignments were fed into axtChain, which 
 organizes all alignments between a single target chromosome and a single
 query chromosome into a group and creates a kd-tree out of the gapless 
 subsections (blocks) of the alignments. A dynamic program was then run over 
 the kd-trees to find the maximally scoring chains of these blocks. Chains 
 scoring below a threshold were discarded; the remaining chains are displayed 
 in this track.</P>
 
 <H2>Credits</H2>
 <P>
 Blastz was developed at <A HREF="http://www.bx.psu.edu/miller_lab/"
 TARGET=_blank>Pennsylvania State University</A> by
 Scott Schwartz, Zheng Zhang, and Webb Miller with advice from
 Ross Hardison.</P>
 <P>
 Lineage-specific repeats were identified by Arian Smit and his
-<A HREF="http://www.repeatmasker.org" TARGET=_blank>RepeatMasker</A>
+<A HREF="https://www.repeatmasker.org/" TARGET=_blank>RepeatMasker</A>
 program.</P>
 <P>
 The axtChain program was developed at the University of California
 at Santa Cruz by Jim Kent with advice from Webb Miller and David Haussler.
 </P>
 <P>
 The browser display and database storage of the chains were generated
 by Robert Baertsch and Jim Kent.</P>
 
 <H2>References</H2>
 <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>
 
 <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>
 
 <P>
 Schwartz S, Kent WJ, Smit A, Zhang Z, Baertsch R, Hardison R,
 Haussler D, Miller W.
 <A HREF="https://genome.cshlp.org/content/13/1/103.abstract"
 TARGET=_blank>Human-Mouse Alignments with BLASTZ</A>.
 <em>Genome Res</em>. 2003 Jan;13(1):103-7.
 PMID: <a href="https://www.ncbi.nlm.nih.gov/pubmed/12529312" target="_blank">12529312</a>; PMC: <a
 href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC430961" target="_blank">PMC430961</a>
 </p>