56a4b894ab60fb7fa7ca3fbec43ccf81a5cdfb84
kuhn
Fri May 21 12:01:18 2021 -0700
fixed typo
diff --git src/hg/makeDb/trackDb/human/revel.html src/hg/makeDb/trackDb/human/revel.html
index a5fe200..08ec086 100644
--- src/hg/makeDb/trackDb/human/revel.html
+++ src/hg/makeDb/trackDb/human/revel.html
@@ -33,31 +33,31 @@
When using this track, zoom in until you can see every basepair at the
top of the display. Otherwise, there are several nucleotides per pixel under
your mouse cursor and instead of an actual score, the tooltip text will show
the average score of all nucleotides under the cursor. This is indicated by
the prefix "~" in the mouseover. Averages of scores are not useful for any
application of REVEL.
REVEL scores are available at the REVEL website. The site provides precomputed REVEL scores for all possible human missense variants -to facilitate the identification of pathogenic variants amoung the large number of +to facilitate the identification of pathogenic variants among the large number of rare variants discovered in sequencing studies.
The REVEL data on the UCSC Genome Browser can be explored interactively with the Table Browser or the Data Integrator. For automated download and analysis, the genome annotation is stored at UCSC in bigWig files that can be downloaded from our download server. The files for this track are called a.bw, c.bw, g.bw, t.bw. Individual regions or the whole genome annotation can be obtained using our tool bigWigToWig which can be compiled from the source code or downloaded as a precompiled binary for your system. Instructions for downloading source code and binaries can be found