b562435c1788de3cc23904a788ba12bfed7a7f72 jnavarr5 Thu Feb 25 14:59:52 2021 -0800 Removing extra colon, refs #18492 diff --git src/hg/makeDb/trackDb/human/caddSuper.html src/hg/makeDb/trackDb/human/caddSuper.html index 9554d13..28c1f1b 100644 --- src/hg/makeDb/trackDb/human/caddSuper.html +++ src/hg/makeDb/trackDb/human/caddSuper.html @@ -32,31 +32,31 @@ score on mouseover.<p> <p> <b>Single nucleotide variants (SNV):</b> For SNVs, at every genome position, there are three values per position, one for every possible nucleotide mutation. The fourth value, "no mutation", e.g. A to A, is always set to zero.<br> When using this track, please zoom in until you can see every basepair at the top of the display. Otherwise, there are several nucleotides under your mouse cursor per pixel and instead of an actual score, the tooltip text can only show the average score of all nucleotides under the cursor, which is indicated by the prefix "~" in the mouseover and averages of scores are not useful for any application of CADD. </p> -<p><b>Insertions and deletions:</b>: Scores are also shown on mouseover for a +<p><b>Insertions and deletions:</b> Scores are also shown on mouseover for a set of insertions and deletions. On hg38, the set has been obtained from Gnomad3. On hg19, the set of indels has been obtained from various sources (gnomAD2, ExAC, 1000 Genomes, ESP). If your insertion or deleletion of interest is not in the track, you will need to use CADD's <a target="_blank" href="https://cadd.gs.washington.edu/score">online scoring tool</a> to obtain them.</p> <h2>Data access</h2> <p> CADD scores are freely available for all non-commercial applications from <a target="_blank" href="https://cadd.gs.washington.edu/download">the CADD website</a>. For commercial applications, see <a target="_blank" href="https://cadd.gs.washington.edu/contact">the license instructions</a> there. </p>