428bacd2dcbaca9304763d3f2dca7ccffd088caa
hiram
  Tue May 26 11:18:06 2020 -0700
correct br tags refs #23734

diff --git src/hg/utils/automation/asmHubNcbiRefSeq.pl src/hg/utils/automation/asmHubNcbiRefSeq.pl
index 48c4d58..60097d0 100755
--- src/hg/utils/automation/asmHubNcbiRefSeq.pl
+++ src/hg/utils/automation/asmHubNcbiRefSeq.pl
@@ -176,95 +176,95 @@
 The RefSeq annotation and RefSeq RNA alignment tracks
 were created at UCSC using data from the NCBI RefSeq project. GFF format
 data files were downloaded from the file <b>${asmId}_genomic.gff.gz</b>
 delivered with the NCBI RefSeq genome assemblies at the FTP location:<br>
 <a href='ftp://ftp.ncbi.nlm.nih.gov/genomes/all/$ftpDirPath/' target='_blank'>ftp://ftp.ncbi.nlm.nih.gov/genomes/all/$ftpDirPath/</a>
 
 The GFF file was converted to the
 genePred and PSL table formats for display in the Genome Browser.
 Information about the NCBI annotation pipeline can be found 
 <a href="https://www.ncbi.nlm.nih.gov/genome/annotation_euk/process/"
 target="_blank">here</a>.
 </p>
 
 <h2>Track statistics summary</h2>
 <p>
-<b>Total genome size: </b>$totalBasesCmfy <b>bases<b></br><br>
+<b>Total genome size: </b>$totalBasesCmfy <b>bases</b><br><br>
 <b>Curated and Predicted Gene count: </b>$itemCount<br>
-<b>Bases in these genes: </b>$basesCovered</br>
-<b>Percent genome coverage: </b>% $percentCoverage</br>
+<b>Bases in these genes: </b>$basesCovered<br>
+<b>Percent genome coverage: </b>% $percentCoverage<br>
 </p>
 
 _EOF_
    ;
 
 if ( -s "$trackDataDir/ncbiRefSeq/${asmId}.ncbiRefSeqCurated.stats.txt" ) {
   $geneStats = `cat $trackDataDir/ncbiRefSeq/${asmId}.ncbiRefSeqCurated.stats.txt | awk '{printf "%d\\n", \$2}' | xargs echo`;
   chomp $geneStats;
   ($itemCount, $basesCovered) = split('\s+', $geneStats);
   $percentCoverage = sprintf("%.3f", 100.0 * $basesCovered / $totalBases);
   $itemCount = commify($itemCount);
   $basesCovered = commify($basesCovered);
   printf <<_EOF_
 <p>
 <b>Curated gene count: </b>$itemCount<br>
-<b>Bases in curated genes: </b>$basesCovered</br>
-<b>Percent genome coverage: </b>% $percentCoverage</br>
+<b>Bases in curated genes: </b>$basesCovered<br>
+<b>Percent genome coverage: </b>% $percentCoverage<br>
 </p>
 _EOF_
 } else {
   printf <<_EOF_
 <p>
 <b>There are no curated gene annotations.</b>
 </p>
 _EOF_
 }
 
 if ( -s "$trackDataDir/ncbiRefSeq/${asmId}.ncbiRefSeqPredicted.stats.txt" ) {
   $geneStats = `cat $trackDataDir/ncbiRefSeq/${asmId}.ncbiRefSeqPredicted.stats.txt | awk '{printf "%d\\n", \$2}' | xargs echo`;
   chomp $geneStats;
   ($itemCount, $basesCovered) = split('\s+', $geneStats);
   $percentCoverage = sprintf("%.3f", 100.0 * $basesCovered / $totalBases);
   $itemCount = commify($itemCount);
   $basesCovered = commify($basesCovered);
   printf <<_EOF_
 <p>
 <b>Predicted gene count: </b>$itemCount<br>
-<b>Bases in genes: </b>$basesCovered</br>
-<b>Percent genome coverage: </b>% $percentCoverage</br>
+<b>Bases in genes: </b>$basesCovered<br>
+<b>Percent genome coverage: </b>% $percentCoverage<br>
 </p>
 _EOF_
 } else {
   printf <<_EOF_
 <p>
 <b>there are no predicted gene annotations</b>
 </p>
 _EOF_
 }
 
 if ( -s "$trackDataDir/ncbiRefSeq/${asmId}.ncbiRefSeqOther.stats.txt" ) {
   $geneStats = `cat $trackDataDir/ncbiRefSeq/${asmId}.ncbiRefSeqOther.stats.txt | awk '{printf "%d\\n", \$2}' | xargs echo`;
   chomp $geneStats;
   ($itemCount, $basesCovered) = split('\s+', $geneStats);
   $percentCoverage = sprintf("%.3f", 100.0 * $basesCovered / $totalBases);
   $itemCount = commify($itemCount);
   $basesCovered = commify($basesCovered);
   printf <<_EOF_
 <p>
 <b>Other annotation count: </b>$itemCount<br>
-<b>Bases in other annotations: </b>$basesCovered</br>
-<b>Percent genome coverage: </b>% $percentCoverage</br>
+<b>Bases in other annotations: </b>$basesCovered<br>
+<b>Percent genome coverage: </b>% $percentCoverage<br>
 </p>
 _EOF_
 }
 
 printf <<_EOF_
 <h2>Credits</h2>
 <p>
 This track was produced at UCSC from data generated by scientists worldwide
 and curated by the NCBI RefSeq project.
 </p>
 
 <h2>References</h2>
 <p>
 Kent WJ.  <a href="https://genome.cshlp.org/content/12/4/656.full"
 target="_blank">BLAT - the BLAST-like alignment tool</a>.