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/human/ntModernHumans.html src/hg/makeDb/trackDb/human/ntModernHumans.html
index a2b93cf..ba4eb8d 100644
--- src/hg/makeDb/trackDb/human/ntModernHumans.html
+++ src/hg/makeDb/trackDb/human/ntModernHumans.html
@@ -18,50 +18,50 @@
 TARGET=_blank>SAM Format Specification</A>
 for more information on the SAM/BAM file format). If a query sequence was
 originally the reverse of what has been stored and aligned, it will have the
 following
 <A HREF="http://samtools.github.io/hts-specs/SAMv1.pdf#page=5"
 TARGET=_blank>flag</A>:
 <PRE>
 (0x10) Read is on '-' strand.
 </PRE></P>
 <P>
 BAM/SAM alignment representations also have <A HREF="http://samtools.github.io/hts-specs/SAMv1.pdf#page=6"
 TARGET=_blank>tags</A>. Some tags are predefined and others (those beginning
 with X, Y or Z) are defined by the aligner or data submitter.
 The following is a list of the tags associated with this track. For this 
 track, those starting with X are specific to the 
-<A HREF="http://bio-bwa.sourceforge.net/"
+<A HREF="https://bio-bwa.sourceforge.net/"
 TARGET=_blank>Burrows-Wheeler Aligner (BWA)</A>.
 <UL>
-<LI><A HREF="http://bio-bwa.sourceforge.net/bwa.shtml"
+<LI><A HREF="https://bio-bwa.sourceforge.net/bwa.shtml"
 TARGET=_blank><B>XT</B></A>: Type: Unique/Repeat/N/Mate-sw</LI>
 <LI><A HREF="http://samtools.github.io/hts-specs/SAMv1.pdf#page=7"
 TARGET=_blank><B>NM</B></A>: Number of nucleotide differences (i.e. edit distance to the reference sequence)</LI>
 <LI><A HREF="http://samtools.github.io/hts-specs/SAMv1.pdf#page=7"
 TARGET=_blank><B>SM</B></A>: Mapping quality if the read is mapped as a single read rather than as a read pair</LI>
 <LI><A HREF="http://samtools.github.io/hts-specs/SAMv1.pdf#page=7"
 TARGET=_blank><B>AM</B></A>: Smaller single-end mapping quality of the two reads in a pair</LI>
-<LI><A HREF="http://bio-bwa.sourceforge.net/bwa.shtml"
+<LI><A HREF="https://bio-bwa.sourceforge.net/bwa.shtml"
 TARGET=_blank><B>X0</B></A>: Number of best hits</LI>
-<LI><A HREF="http://bio-bwa.sourceforge.net/bwa.shtml"
+<LI><A HREF="https://bio-bwa.sourceforge.net/bwa.shtml"
 TARGET=_blank><B>X1</B></A>: Number of suboptimal hits found by BWA</LI>
-<LI><A HREF="http://bio-bwa.sourceforge.net/bwa.shtml"
+<LI><A HREF="https://bio-bwa.sourceforge.net/bwa.shtml"
 TARGET=_blank><B>XM</B></A>: Number of mismatches in the alignment</LI>
-<LI><A HREF="http://bio-bwa.sourceforge.net/bwa.shtml"
+<LI><A HREF="https://bio-bwa.sourceforge.net/bwa.shtml"
 TARGET=_blank><B>XO</B></A>: Number of gap opens</LI>
-<LI><A HREF="http://bio-bwa.sourceforge.net/bwa.shtml"
+<LI><A HREF="https://bio-bwa.sourceforge.net/bwa.shtml"
 TARGET=_blank><B>XG</B></A>: Number of gap extentions</LI>
 <LI><A HREF="http://samtools.github.io/hts-specs/SAMv1.pdf#page=7"
 TARGET=_blank><B>MD</B></A>: String for mismatching positions in the format of [0-9]+(([ACGTN]|\^[ACGTN]+)[0-9]+)*</LI>
        </UL>
         </LI>
 </UL>
 </P>
 <P>
 The item labels and display colors of features within this track can be
 configured through the controls at the top of the track description page.
 </P>
 <UL>
 <LI><B>Display Read Names</B>: By default, read names are not displayed. To 
 display the read names, selected the check box next to "Display read names".
 </LI>
@@ -97,31 +97,31 @@
     When &quot;unpaired ends&quot; is selected, items that were paired in 
     sequencing but whose mate was not mapped are colored gray, while singletons 
     and properly paired items are black. Alignment quality is the default.</LI>
     </UL>
     </LI>
 </UL>
 </P>
 
 <H2>Methods</H2>
 <P>
 The genomes of a San individual from Southern Africa (HGDP01029), a Yoruba
 individual from West Africa (HGDP00927), a Han Chinese individual (HGDP00778), 
 an individual from Papua New Guinea (HGDP00542), and a French individual
 (HGDP00521) from Western Europe were sequenced to 4- to 6-fold coverage on
 the Illumina GAII platform. These sequences were aligned to the human
-reference genome (NCBI36/hg18) using the <A HREF="http://bio-bwa.sourceforge.net/"
+reference genome (NCBI36/hg18) using the <A HREF="https://bio-bwa.sourceforge.net/"
 TARGET=_blank>Burrows-Wheeler Aligner (BWA)</A>. Reads with an alignment
 quality of less than 30 were not included in these data. Those with an alignment
 quality greater than or equal to 30 were analyzed using a similar approach to
 that used for the Neandertal data.
 </P>
 
 <H2>Credits</H2>
 <P>
 This track was produced at UCSC using data generated by
 <A HREF="mailto:&#101;&#100;&#64;&#115;&#111;e.&#117;&#99;s&#99;.&#101;&#100;&#117;"
 title="&#101;&#100;&#64;&#115;&#111;e.&#117;&#99;s&#99;.&#101;&#100;&#117;" rel="nofollow"
 TARGET=_BLANK>Ed Green</A>.
 </P>
 
 <H2>References</H2>