--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/test_MACS2.1.2_peaks.xls	Wed Dec 12 08:26:16 2018 -0500
@@ -0,0 +1,32 @@
+#peaks file
+# This file is generated by MACS version 2.1.2
+# Command line: callpeak -t /tmp/tmpKNHGvp/files/000/dataset_2.dat -c /tmp/tmpKNHGvp/files/000/dataset_1.dat --format=BED --name=test_MACS2.1.2 --bw=300 --gsize=775000000.0 --nomodel --extsize=243 --qvalue=0.05 -B --SPMR --mfold 5 50 --keep-dup 1
+# ARGUMENTS LIST:
+# name = test_MACS2.1.2
+# format = BED
+# ChIP-seq file = ['/tmp/tmpKNHGvp/files/000/dataset_2.dat']
+# control file = ['/tmp/tmpKNHGvp/files/000/dataset_1.dat']
+# effective genome size = 7.75e+08
+# band width = 300
+# model fold = [5, 50]
+# qvalue cutoff = 5.00e-02
+# The maximum gap between significant sites is assigned as the read length/tag size.
+# The minimum length of peaks is assigned as the predicted fragment length "d".
+# Larger dataset will be scaled towards smaller dataset.
+# Range for calculating regional lambda is: 1000 bps and 10000 bps
+# Broad region calling is off
+# Paired-End mode is off
+# MACS will save fragment pileup signal per million reads
+
+# tag size is determined as 50 bps
+# total tags in treatment: 50
+# tags after filtering in treatment: 50
+# maximum duplicate tags at the same position in treatment = 1
+# Redundant rate in treatment: 0.00
+# total tags in control: 50
+# tags after filtering in control: 50
+# maximum duplicate tags at the same position in control = 1
+# Redundant rate in control: 0.00
+# d = 243
+#chr	start	end	length	abs_summit	pileup	-log10(pvalue)	fold_enrichment	-log10(qvalue)	name
+chr26	4118914	4119282	369	4119130	9.00	9.13132	6.31632	2.51561	test_MACS2.1.2_peak_1