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Showing 2 changed files with 38 additions and 2 deletions.
5 changes: 3 additions & 2 deletions grails-app/i18n/informational.properties
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@@ -364,6 +364,7 @@ informational.shared.traits.anyStroke=any stroke
informational.shared.traits.qrs=QRS interval duration
informational.shared.traits.adiponectin=adiponectin levels
informational.shared.traits.leptin=leptin levels
informational.shared.traits.leptinAdjBMI=leptin levels adjusted for BMI
informational.shared.traits.allDKD=all diabetic kidney disease
informational.shared.traits.CKDpDKD=chronic kidney disease and diabetic kidney disease
informational.shared.traits.CKD=chronic kidney disease
@@ -2183,7 +2184,7 @@ informational.data.accessing.HPTxNCGM1=Han population Taiwan-NGCM results are av
informational.data.accessing.HPTxNCGM2= tool</li>\
<li>From the <b>View full genetic association results for a phenotype</b> search on the home page: first select one of the phenotypes listed above, \
and then on the resulting page, select the Han population Taiwan-NGCM dataset.</li></ul>
informational.data.download.70KforT2D=<a href="http://cg.bsc.es/70kfort2d/" target="_blank">Download full summary statistics</a>
informational.data.download.70KforT2D=<a href="http://cg.bsc.es/70kfort2d/" target="_blank">Download summary statistics</a>
informational.data.exptsumm.DIAGRAM1000G1=The DIAGRAM 1000G GWAS meta-analysis (Stage 1) was published by Scott et al. (see citation above). \
GWAS data were included from 18 studies, comprising a total of 26,676 T2D cases and 132,532 control participants. Single-nucleotide \
polymorphisms were imputed for both autosomes and the X chromosome using the all ancestries 1000 Genomes Project (1000G) reference \
@@ -2388,7 +2389,7 @@ informational.data.overview.FUSION_Metabochip3=No variants in either model reach
informational.data.overlaps.ExTex1=Note that the samples in the GoT2D exome chip analysis and FUSION exome chip analysis datasets are a subset of those included in the \
ExTexT2D exome chip analysis dataset.
informational.data.overlaps.ExTex2=Cases in the EXTEND GWAS dataset are included in the ExTexT2D exome chip analysis dataset.
informational.data.download.BFpercent=<a href="https://walker05.u.hpc.mssm.edu/" target="_blank">Download full summary statistics</a>
informational.data.download.BFpercent=<a href="https://walker05.u.hpc.mssm.edu/" target="_blank">Download summary statistics</a>
informational.data.exptsumm.BFpercent=This study is a meta-analysis, combining results of body fat percentage genetic associations \
for up to 100,716 individuals from 43 GWAS (<i>n</i> up to 76,137) and 13 MetaboChip studies (<i>n</i> up to 24,582), predominantly of European \
ancestry (<i>n</i> up to 89,297), but also of non-European ancestry (<i>n</i> up to 11,419).
35 changes: 35 additions & 0 deletions grails-app/views/informational/data/_GWAS_Leptin.gsp
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@@ -1,2 +1,37 @@
<script class="panel-body" id="GWAS_Leptin_script" type="x-tmpl-mustache">
<h4><g:message code="informational.shared.headers.dataset"></g:message></h4>
<p><g:message code="informational.data.download.BFpercent"></g:message></p>
<h4><g:message code="informational.shared.headers.publications"></g:message></h4>
<p><div class="paper">
<g:message code="informational.shared.publications.Kilpelainen_2016_NatCommun"></g:message><br>
<g:message code="informational.shared.publications.Kilpelainen_2016_NatCommun.author"></g:message><g:message code="informational.shared.publications.etal"></g:message>
<div class="citation"><g:message code="informational.shared.publications.Kilpelainen_2016_NatCommun.citation"></g:message> </div>
</div></p>
<h4><g:message code="informational.shared.headers.dataset_pheno"></g:message></h4>
<ul>
<li><g:message code="informational.shared.traits.leptin"></g:message></li>
<li><g:message code="informational.shared.traits.leptinAdjBMI"></g:message></li>
</ul>
<h4><g:message code="informational.shared.headers.dataset_subjects"></g:message></h4>
<table class="table table-condensed table-responsive table-striped">
<tr><th>Samples</th><th>Cohort</th><th>Ancestry</th></tr>
</table>
<h4><g:message code="informational.shared.headers.exptsumm"></g:message></h4>
<p><g:message code="informational.data.exptsumm.Leptin_GWAS"></g:message></p>
<h4>Accessing ADIPOGen GWAS data</h4>
<p><g:message code="informational.data.accessing.Leptin_GWAS1"></g:message> <a href="${createLink(controller: 'variantSearch', action: 'variantSearchWF')}">Variant Finder</a> <g:message code="informational.data.accessing.Leptin_GWAS2"></g:message></p>
</script>

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