021de8301f32cdd5576b80baa7db03a8edc8d60a
abenetpa
  Wed Sep 16 01:19:33 2020 -0700
changed P value to p-value refs #26129

diff --git src/hg/makeDb/trackDb/human/covidHgiGwas.html src/hg/makeDb/trackDb/human/covidHgiGwas.html
index 88d2789..0cf3be2 100644
--- src/hg/makeDb/trackDb/human/covidHgiGwas.html
+++ src/hg/makeDb/trackDb/human/covidHgiGwas.html
@@ -1,99 +1,99 @@
 <H2>Description</H2>
 <p>
 This track set shows <b>GWAS meta-analyses</b> from the 
 <a target=_blank href="https://www.covid19hg.org/">
 <b>COVID-19 Host Genetics Initiative (HGI)</b></a>: 
 a collaborative effort to facilitate 
 the generation, analysis and sharing of COVID-19 host genetics research.
 The COVID-19 HGI organizes meta-analyses across multiple studies contributed by 
 <a target="_blank" href="https://www.covid19hg.org/partners/">partners world-wide</a>
 to identify the genetic determinants of SARS-CoV-2 infection susceptibility and disease severity 
 and outcomes. Moreover, the COVID-19 HGI also aims to provide a platform for study partners to 
 share analytical results in the form of summary statistics and/or individual level data where 
 possible.
 </p>
 
 <p>
 The specific phenotypes studied by the COVID-19 HGI are those that benefit from maximal sample 
 size: primary analysis on disease severity. Two meta-analyses are represented in this track:
 </p>
 
 <ul>
 <li><b>ANA_C2_V2</b>: covid vs. population (6696 cases from 18 studies)</li>
 <li><b>ANA_B2_V2</b>: hospitalized covid vs. population (3199 cases from 8 studies)</li>
 </ul>
 
 <H2>Display Conventions</H2>
 <p>
 Displayed items are colored by <b>GWAS effect</b>:  red for positive, blue for negative. 
 The height of the item reflects the <b>effect size</b> (beta coefficient).
-The color saturation indicates <b>statistical significance</b>: <em>P</em> values smaller than .05
+The color saturation indicates <b>statistical significance</b>: p-values smaller than .05
 are brightly colored (bright red
 <span style='background-color: #ff0000;'>&nbsp;&nbsp;</span>
 , bright blue
 <span style='background-color: #0000ff;'>&nbsp;&nbsp;</span>
 ),
-those with less significance (<em>P</em> >= .05) are paler (light red
+those with less significance (p >= .05) are paler (light red
 <span style='background-color: #ffa0a0;'>&nbsp;&nbsp;</span>
 , light blue
 <span style='background-color: #a0a0ff;'>&nbsp;&nbsp;</span>
-). For better visualization of the data, only SNPs with <em>P</em> values smaller than .03 are 
+). For better visualization of the data, only SNPs with p-values smaller than .03 are 
 displayed by default. 
 </p>
 
 <p>
 Each track has separate display controls and data can be filtered according to the
-<b>number of studies</b>, <b>minimum -log10 <em>P</em> value</b>, and the
+<b>number of studies</b>, <b>minimum -log10 p-value</b>, and the
 <b>effect size (beta coefficient)</b>, using the track <b>Configure</b> options.
 </p>
 
 <p>
 <b>Mouseover</b> on items shows the rs ID (or chrom:pos if none assigned), both the non-effect 
-and effect alleles, the effect size (beta coefficient), the <em>P</em> value, and the number of 
+and effect alleles, the effect size (beta coefficient), the p-value, and the number of 
 studies.
 Additional information on each variant can be found on the details page by clicking on the item.
 </p>  
 
 <H2>Methods</H2>
 <p>
 Data were generated from genome-wide SNP array and whole exome and genome sequencing: leveraging 
 the impact of both common and rare variants. The statistical analysis performed takes into account 
 differences between sex, ancestry, and date of sample collection. More information about the 
 prospective studies, processing pipeline, results and data sharing can be found 
 <a target=_blank href="https://www.covid19hg.org/about/">here</a>.
 </p>
 
 
 <H2>Data Access</H2>
 <p>
 The data underlying these tracks and summary statistics results are publicly available in 
 <a target=_blank href="https://www.covid19hg.org/results">COVID19-hg Release 3 (June 2020)</a>.
 The raw data can be explored interactively with the <a target="_blank" href="../cgi-bin/hgTables">
 Table Browser</a>, or the <a target="_blank" href="../cgi-bin/hgIntegrator">Data Integrator</a>. 
 Please refer to
 our <a href="https://groups.google.com/a/soe.ucsc.edu/forum/#!forum/genome"
 target="_blank">mailing list archives</a> for questions, or our <a target="_blank"
 href="../FAQ/FAQdownloads.html#download36">Data Access FAQ</a> for more information.
 </p>
 
 <H2>Credits</H2>
 <p>
 Thanks to the COVID-19 Host Genetics Initiative contributors and project leads for making these 
 data available, and in particular to Rachel Liao, Juha Karjalainen, and Kumar Veerapen at the 
 Broad Institute for their review and input during browser track development.
 </p>
 
 <H2>References</H2>
 
 <p>
 COVID-19 Host Genetics Initiative.
 <a href="https://www.ncbi.nlm.nih.gov/pubmed/32404885" target="_blank">
 The COVID-19 Host Genetics Initiative, a global initiative to elucidate the role of host genetic
 factors in susceptibility and severity of the SARS-CoV-2 virus pandemic</a>.
 <em>Eur J Hum Genet</em>. 2020 Jun;28(6):715-718.
 PMID: <a href="https://www.ncbi.nlm.nih.gov/pubmed/32404885" target="_blank">32404885</a>; PMC: <a
 href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7220587/" target="_blank">PMC7220587</a>
 </p>