diff --git a/test/test_extensive.sh b/test/test_extensive.sh
index 8fef0cf..a06f83b 100755
--- a/test/test_extensive.sh
+++ b/test/test_extensive.sh
@@ -8,5 +8,7 @@ die() {
 }
 
 test/test_identity.sh || die "test_identity.sh failed"
+test/test_meth.sh || die "test_meth.sh failed"
+test/test_misc.sh || die "test_misc.sh failed"
 
 echho "all done"
\ No newline at end of file
diff --git a/test/test_meth.sh b/test/test_meth.sh
index 005588d..a304663 100755
--- a/test/test_meth.sh
+++ b/test/test_meth.sh
@@ -10,18 +10,23 @@ die() {
 REF_HG38=/genome/hg38noAlt.fa
 REF_HG38_IDX=/genome/hg38noAlt.idx
 
-#should download the following
+# should download the following from aws
 METH_TRUTH=/home/hasindu/scratch/hg2_prom_lsk114_5khz/guppy_6.5.7_hac/PGXXXX230339_guppy657hac_mm226_f5c13_mfreq.tsv
 
 MINIMOD=/data/hasindu/hasindu2008.git/minimod/minimod
 COMPARE=~/hasindu2008.git/f5c/scripts/compare_methylation.py
 
+REMOVE_TMP(){
+    rm -f new.blow5 new.sam new.bam new.bam.bai new.bedmethyl methcomp.tsv a.acc a.log
+}
+
+REMOVE_TMP
+test -e meth.tsv && rm meth.tsv
+test -e ref_chr22.fa && rm ref_chr22.fa
+
 tail -n +2 $METH_TRUTH | grep -w "chr22" | cut -f 1,2,7 > meth.tsv || die "failed extracting chr, pos, meth_freq"
 samtools faidx ${REF_HG38} chr22 > ref_chr22.fa || die "failed extracting chr22 from ref"
 
-test -e new.blow5 && rm new.blow5
-test -e new.fastq && rm new.fastq
-
 CHECK_ACC(){
     THRESH=$1
     FILE=$2
@@ -37,24 +42,22 @@ CHECK_ACC(){
     echo ""
 }
 
-REMOVE_TMP(){
-    rm -f new.blow5 new.sam new.bam new.bedmethyl methcomp.tsv a.acc a.log
-}
+
 
 RUN_TEST(){
     PROF=$1
     MODEL=$2
     ./squigulator ref_chr22.fa -x ${PROF} -f 10 -t 20 -o new.blow5 --meth-freq meth.tsv 2> a.log || die "squigulator failed"
-    eel  -i new.blow5 --config ${MODEL} --device cuda:all -o new.sam --call_mods &>> a.log|| die "eel failed"
-    samtools fastq -TMM,ML new.sam  | minimap2 -ax map-ont -y -Y --secondary=no ref_chr22.fa - | samtools sort - -o new.bam 2>> a.log || die "samtools failed"
+    eel  -i new.blow5 --config ${MODEL} --device cuda:all -o new.sam --call_mods &>> a.log || die "eel failed"
+    samtools fastq -TMM,ML new.sam  2>> a.log  | minimap2 -ax map-ont -y -Y --secondary=no ref_chr22.fa -  2>> a.log | samtools sort - -o new.bam  2>> a.log || die "samtools failed"
     samtools index new.bam || die "samtools index failed"
     # /install/modkit-v0.1.13/modkit pileup --cpg --ref ref_chr22.fa --ignore h -t 32 new.bam  new.tmp.bedmethyl
     # grep "chr22" new.tmp.bedmethyl |  grep -v nan  > new.bedmethyl
     ${MINIMOD} mod-freq ref_chr22.fa new.bam -b > new.bedmethyl 2>> a.log || die "minimod failed"
     ${COMPARE} ${METH_TRUTH} new.bedmethyl > methcomp.tsv 2>> a.log || die "compare failed"
-    tail -n+2 methcomp.tsv | datamash ppearson 3:5 2>> a.acc || die "pearson failed"
+    tail -n+2 methcomp.tsv | datamash ppearson 3:5 > a.acc || die "pearson failed"
     # ~/hasindu2008.git/f5c/scripts/plot_methylation.R  -i methcomp.tsv -o methcomp.pdf
-    # cat a.acc
+    cat a.acc
     CHECK_ACC 0.92 a.acc
     REMOVE_TMP
 }
diff --git a/test/test_misc.sh b/test/test_misc.sh
index cdf5d8c..3702f5f 100755
--- a/test/test_misc.sh
+++ b/test/test_misc.sh
@@ -7,13 +7,18 @@ die() {
     exit 1
 }
 
-REF_HG38=/genome/hg38noAlt.fa
-REF_HG38_IDX=/genome/hg38noAlt.idx
 
 REF_GENCODE=/genome/gencode.v40.transcripts.fa
 
-test -e new.blow5 && rm new.blow5
-test -e new.fastq && rm new.fastq
+REF_TRANS_BAM=/home/hasindu/scratch/uhr_prom_rna004/PNXRXX240011_reads_500k.bam
+
+REMOVE_TMP(){
+    rm -f new.blow5 new.fastq a.acc a.log a.paf count_joined.tsv count_new.tsv
+}
+
+REMOVE_TMP
+test -e count.tsv && rm count.tsv
+
 
 CHECK_ACC(){
     THRESH=$1
@@ -30,10 +35,28 @@ CHECK_ACC(){
     echo ""
 }
 
-REMOVE_TMP(){
-    rm -f new.blow5 new.fastq a.acc a.log
-}
 
 
+samtools  view PNXRXX240011_reads_500k.bam | cut -f 3 | sort | uniq -c | awk '{print $2"\t"$1}' | sort -k1,1 > count.tsv || die "failed extracting chr, pos, meth_freq"
 
+RUN_REST(){
+    minimap2 -cx map-ont -y -Y --secondary=no ${REF_GENCODE} new.fastq > a.paf  2>> a.log
+    cat a.paf | cut -f 6 | sort | uniq -c | awk '{print $2"\t"$1}' -k1,1 > count_new.tsv || die "failed getting counts"
+    join count.tsv count_new.tsv > count_joined.tsv || die "failed joining counts"
+    cat count_joined.tsv | datamash ppearson 2:3 > a.acc || die "pearson failed"
+    cat a.acc
+    CHECK_ACC 0.95 a.acc
+    REMOVE_TMP
+}
 
+PROF=rna004-prom
+MODEL=rna_rp4_130bps_hac_prom.cfg
+./squigulator ${REF_GENCODE} -x ${PROF}  -t 20 -o new.blow5 --trans-count count.tsv 2> a.log || die "squigulator failed"
+eel  -i new.blow5 --config ${MODEL} --device cuda:all -o new.fastq  &>> a.log || die "eel failed"
+RUN_REST
+
+PROF=dna-r9-prom
+MODEL=dna_r9.4.1_450bps_hac_prom.cfg
+./squigulator ${REF_GENCODE} -x ${PROF} -t 20 -o new.blow5 --trans-count count.tsv --cdna 2> a.log || die "squigulator failed"
+eel  -i new.blow5 --config ${MODEL} --device cuda:all -o new.fastq  &>> a.log || die "eel failed"
+RUN_REST
\ No newline at end of file