582f5ea34df7defd80c6ea88ff7cd8a845441506
jnavarr5
  Thu Oct 24 16:28:34 2019 -0700
Updating a redirected link on the lrg track, refs #24285

diff --git src/hg/makeDb/trackDb/human/lrg.html src/hg/makeDb/trackDb/human/lrg.html
index 3271c7c..93ce4db 100644
--- src/hg/makeDb/trackDb/human/lrg.html
+++ src/hg/makeDb/trackDb/human/lrg.html
@@ -1,61 +1,60 @@
 <H2>Description</H2>
 <P>
 <A HREF="http://www.lrg-sequence.org/"
 TARGET=_BLANK>Locus Reference Genomic (LRG)</A>
 sequences are manually curated, stable DNA sequences that surround a
 locus (typically a gene) and provide an unchanging coordinate system
 for reporting sequence variants.  They are not necessarily identical
 to the corresponding sequence in a particular reference genome
 assembly (such as $date), but can be mapped to each version of a
 reference genome assembly in order to convert between the stable LRG
 variant coordinates and the various assembly coordinates.
 </P>
 <P>
 Each LRG record also includes at least one stable transcript
 on which variants may be reported.  These transcripts
 appear in the LRG Transcripts track in the Gene and Gene Predictions
 track section.</P>
 
 <H2>Methods</H2>
 <P>
 LRG sequences are suggested by the community studying a locus (for example,
 Locus-Specific Database curators, research laboratories, mutation consortia).
 LRG curators then examine the submitted transcript as well as other known
 transcripts at the locus, in the context of alignment and public expression
 data.
 For more information on the selection and annotation process, see the 
 <A HREF="http://www.lrg-sequence.org/faq/" TARGET=_BLANK>LRG FAQ</A>,
 (Dalgleish, <em>et al.</em>) and (MacArthur, <em>et al.</em>).
 </P>
 
 <H2>Credits</H2>
 <P>
 This track was produced at UCSC using
 <A HREF="ftp://ftp.ebi.ac.uk/pub/databases/lrgex/" TARGET=_BLANK>LRG XML files</A>.
 Thanks to
 <A HREF="http://www.lrg-sequence.org/documentation/lrg-collaborators/" TARGET=_BLANK>LRG collaborators</A>
 for making these data available.
 </P>
 
 <H2>References</H2>
 <p>
 Dalgleish R, Flicek P, Cunningham F, Astashyn A, Tully RE, Proctor G, Chen Y, McLaren WM, Larsson P,
 Vaughan BW <em>et al</em>.
 <a href="https://genomemedicine.biomedcentral.com/articles/10.1186/gm145" target="_blank"> 
 Locus Reference Genomic sequences: an improved basis for describing human DNA variants</a>.
 <em>Genome Med</em>. 2010 Apr 15;2(4):24.
 PMID: <a href="https://www.ncbi.nlm.nih.gov/pubmed/20398331" target="_blank">20398331</a>; PMC: <a
 href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2873802/" target="_blank">PMC2873802</a> 
 </p>
 
 <p>
 MacArthur JA, Morales J, Tully RE, Astashyn A, Gil L, Bruford EA, Larsson P, Flicek P, Dalgleish R,
 Maglott DR <em>et al</em>.
-<a href="https://academic.oup.com/nar/article/42/D1/D873/1059919/Locus-Reference-Genomic-reference-
-sequences-for" target="_blank">
+<a href="https://academic.oup.com/nar/article/42/D1/D873/1059919" target="_blank">
 Locus Reference Genomic: reference sequences for the reporting of clinically relevant sequence
 variants</a>.
 <em>Nucleic Acids Res</em>. 2014 Jan;42(Database issue):D873-8.
 PMID: <a href="https://www.ncbi.nlm.nih.gov/pubmed/24285302" target="_blank">24285302</a>; PMC: <a
 href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3965024/" target="_blank">PMC3965024</a>
 </p>