--- a/macros.xml	Fri Jun 30 07:58:35 2023 +0000
+++ b/macros.xml	Mon Aug 07 01:36:34 2023 +0000
@@ -12,8 +12,8 @@
             <xref type="bioconductor">dada2</xref>
         </xrefs>
     </xml>
-    <token name="@DADA2_VERSION@">1.20</token>
-    <token name="@WRAPPER_VERSION@">1</token>
+    <token name="@DADA2_VERSION@">1.28</token>
+    <token name="@WRAPPER_VERSION@">0</token>
 
     <xml name="version_command">
         <version_command><![CDATA[
@@ -43,17 +43,18 @@
          - uniques is a named integer vector (columns=ASVs, only one rows)-->
     <token name="@READ_FOO@"><![CDATA[
     read.uniques <- function ( fname ) {
-         p <- read.table(fname, header=F, sep="\t")
+         x <- read.table(fname, header=F, sep="\t")
          n <-x[,2]
          names(n)<-x[,1]
+         return(n)
     }
     #def read_data($dataset)
         #if $dataset.is_of_type('dada2_sequencetable')
-            t(as.matrix( read.table('$dataset', header=T, sep="\t", row.names=1) ))
+            t(read.table('$dataset', header=T, sep="\t", row.names=1, check.names=FALSE))
         #else if $dataset.is_of_type('dada2_uniques')
             read.uniques('$dataset')
         #else if $dataset.is_of_type('tabular')
-            read.table('$dataset', header=T, sep="\t", row.names=1)
+            read.table('$dataset', header=T, sep="\t", row.names=1, check.names=FALSE)
         #else
             readRDS('$dataset')
         #end if
@@ -97,7 +98,7 @@
 
     <!-- for filterAndTrim -->
     <xml name="trimmers">
-        <section name="trim" title="Trimming parameters">
+        <section name="trim" title="Trimming parameters" expanded="true">
             <param argument="truncQ" type="integer" value="2" min="0" label="Truncate reads at quality threshold" help="Truncate reads at the first instance of a quality score less than or equal to this threshold"/>
             <param argument="trimLeft" type="integer" value="0" min="0" label="Trim start of each read" help="The number of nucleotides to remove from the start of each read."/>
             <param argument="trimRight" type="integer" value="0" min="0" label="Trim end of each read" help="The number of nucleotides to remove from the end of each read"/>
@@ -105,7 +106,7 @@
         </section>
     </xml>
     <xml name="filters">
-        <section name="filter" title="Filtering parameters">
+        <section name="filter" title="Filtering parameters" expanded="true">
             <param argument="maxLen" type="integer" value="" optional="true" min="0" label="Remove long reads" help="Remove reads with length greater than this value. Default: no length threshold"/>
             <param argument="minLen" type="integer" value="20" min="0" label="Remove short reads" help="Remove reads with length less than this value. Default: 20"/>
             <param argument="maxN" type="integer" value="0" min="0" label="Remove reads with more Ns" help="Note that some of the subsequent dada pipeline steps do not allow Ns"/>

--- a/test-data/gentest.R	Fri Jun 30 07:58:35 2023 +0000
+++ b/test-data/gentest.R	Mon Aug 07 01:36:34 2023 +0000
@@ -11,9 +11,9 @@
 print("filterAndTrim")
 
 for (i in seq_len(fwd)) {
-    ftout <- dada2::filterAndTrim(fwd[i], filt_fwd[i], rev[i], filt_rev[i])
-    b <- paste(strsplit(fwd[i], ".", fixed = TRUE)[[1]][1], "tab", sep = ".")
-    write.table(ftout, b, quote = FALSE, sep = "\t", col.names = NA)
+  ftout <- dada2::filterAndTrim(fwd[i], filt_fwd[i], rev[i], filt_rev[i])
+  b <- paste(strsplit(fwd[i], ".", fixed = TRUE)[[1]][1], "tab", sep = ".")
+  write.table(ftout, b, quote = FALSE, sep = "\t", col.names = NA)
 }
 
 # In the test only the 1st data set is used
@@ -64,15 +64,15 @@
 dada_fwd <- dada2::dada(filt_fwd, err_fwd)
 dada_rev <- dada2::dada(filt_rev, err_rev)
 for (id in sample_names) {
-    saveRDS(dada_fwd[[id]], file = paste("dada_", id, "_R1.Rdata", sep = ""))
-    saveRDS(dada_rev[[id]], file = paste("dada_", id, "_R2.Rdata", sep = ""))
+  saveRDS(dada_fwd[[id]], file = paste("dada_", id, "_R1.Rdata", sep = ""))
+  saveRDS(dada_rev[[id]], file = paste("dada_", id, "_R2.Rdata", sep = ""))
 }
 
 # merge pairs
 print("mergePairs")
 merged <- dada2::mergePairs(dada_fwd, filt_fwd, dada_rev, filt_rev)
 for (id in sample_names) {
-    saveRDS(merged[[id]], file = paste("mergePairs_", id, ".Rdata", sep = ""))
+  saveRDS(merged[[id]], file = paste("mergePairs_", id, ".Rdata", sep = ""))
 }
 
 
@@ -85,8 +85,8 @@
 df <- data.frame(length = as.numeric(names(reads_per_seqlen)), count = reads_per_seqlen)
 pdf("makeSequenceTable.pdf")
 ggplot(data = df, aes(x = length, y = count)) +
-    geom_col() +
-    theme_bw()
+  geom_col() +
+  theme_bw()
 bequiet <- dev.off()
 
 # remove bimera
@@ -119,7 +119,7 @@
 
 merged_nondef <- dada2::mergePairs(dada_fwd, filt_fwd, dada_rev, filt_rev, minOverlap = 8, maxMismatch = 1, justConcatenate = TRUE, trimOverhang = TRUE)
 for (id in sample_names) {
-    saveRDS(merged_nondef[[id]], file = paste("mergePairs_", id, "_nondefault.Rdata", sep = ""))
+  saveRDS(merged_nondef[[id]], file = paste("mergePairs_", id, "_nondefault.Rdata", sep = ""))
 }
 rb_dada_fwd <- dada2::removeBimeraDenovo(dada_fwd[["F3D0_S188_L001"]])
 write.table(rb_dada_fwd, file = "removeBimeraDenovo_F3D0_dada_uniques.tab", quote = FALSE, sep = "\t", row.names = TRUE, col.names = FALSE)
@@ -129,7 +129,7 @@
 
 # SeqCounts
 get_n <- function(x) {
-    sum(dada2::getUniques(x))
+  sum(dada2::getUniques(x))
 }
 
 print("seqCounts ft")