# HG changeset patch
# User iuc
# Date 1657724484 0
# Node ID 245d50e9ac220705f74b94ef057c60a16a914d55
# Parent  2220b0dc7d122355a237ce0a30e433c6b5d7f70d
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/gemini commit f7bdf08922aaf4119aefe7041e754a69cf64aebd

diff -r 2220b0dc7d12 -r 245d50e9ac22 gemini_macros.xml
--- a/gemini_macros.xml	Tue Aug 31 08:21:31 2021 +0000
+++ b/gemini_macros.xml	Wed Jul 13 15:01:24 2022 +0000
@@ -184,7 +184,7 @@
         <repeat name="regions" title="Region Filter" default="0" min="0"
         help="Filter variant sites by their position in the genome. If multiple Region Filters are specified, all variants that fall in ONE of the regions are reported.">
             <param name="chrom" type="text" label="Chromosome">
-                <validator type="expression" message="A chromosome identifier is required when specifying a region filter">value.strip()</validator>
+                <validator type="regex" message="A chromosome identifier is required when specifying a region filter. It should start with 'chr'">^chr[0-9a-zA-Z: _.-]+</validator>
             </param>
             <param name="start" type="text" label="Region Start">
                 <validator type="expression" message="an integer number is required">not value or value.isdigit()</validator>
diff -r 2220b0dc7d12 -r 245d50e9ac22 test-data/gemini_region_filter.tabular
--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/gemini_region_filter.tabular	Wed Jul 13 15:01:24 2022 +0000
@@ -0,0 +1,39 @@
+chrom	start	end	ref	alt	gene	impact
+chr1	10582	10583	G	A	DDX11L1	upstream_gene_variant
+chr1	10610	10611	C	G	DDX11L1	upstream_gene_variant
+chr1	13301	13302	C	T	DDX11L1	exon_variant
+chr1	13326	13327	G	C	DDX11L1	exon_variant
+chr1	13956	13958	TC	T	DDX11L1	exon_variant
+chr1	13979	13980	T	C	DDX11L1	exon_variant
+chr1	30922	30923	G	T	FAM138A	downstream_gene_variant
+chr1	46401	46402	C	CTGT	None	intergenic_variant
+chr1	47189	47190	G	GA	None	intergenic_variant
+chr1	51475	51476	T	C	None	intergenic_variant
+chr1	51478	51479	T	A	None	intergenic_variant
+chr1	51913	51914	T	G	None	intergenic_variant
+chr1	51934	51935	C	T	None	intergenic_variant
+chr1	51953	51954	G	C	None	intergenic_variant
+chr1	52057	52058	G	C	None	intergenic_variant
+chr1	52143	52144	T	A	None	intergenic_variant
+chr1	52184	52188	TTAA	T	None	intergenic_variant
+chr1	52237	52238	T	G	None	intergenic_variant
+chr1	53233	53236	CAT	C	None	intergenic_variant
+chr1	54352	54353	C	A	None	intergenic_variant
+chr1	54420	54421	A	G	None	intergenic_variant
+chr1	54489	54490	G	A	None	intergenic_variant
+chr1	54675	54676	C	T	None	intergenic_variant
+chr1	54752	54753	T	G	None	intergenic_variant
+chr1	55163	55164	C	A	None	intergenic_variant
+chr1	55248	55249	C	CTATGG	None	intergenic_variant
+chr1	55298	55299	C	T	None	intergenic_variant
+chr1	55312	55313	A	T	None	intergenic_variant
+chr1	55325	55326	T	C	None	intergenic_variant
+chr1	55329	55330	G	A	None	intergenic_variant
+chr1	55366	55367	G	A	None	intergenic_variant
+chr1	55387	55388	C	T	None	intergenic_variant
+chr1	55393	55394	T	A	None	intergenic_variant
+chr1	55415	55416	G	A	None	intergenic_variant
+chr1	55426	55427	T	C	None	intergenic_variant
+chr1	55815	55816	G	A	None	intergenic_variant
+chr1	55849	55850	C	G	None	intergenic_variant
+chr1	55851	55852	G	C	None	intergenic_variant