diff --git a/wolf_tutorial.md b/wolf_tutorial.md
index 2577aab..45be4db 100644
--- a/wolf_tutorial.md
+++ b/wolf_tutorial.md
@@ -49,15 +49,21 @@ Not working yet...
 
 ### 1. Import the sequencing data in a DMS
 
+Download the reads:
+
+[wolf_F.fastq.gz](/uploads/09dada3587189c3b3a7af7024981c074/wolf_F.fastq.gz)
+
+[wolf_R.fastq.gz](/uploads/a95dbad14b75474c8307cab56fa083ca/wolf_R.fastq.gz)
+
 1. Import the first set of reads, with :
 
-		obi import --quality-solexa wolf_tutorial/wolf_F.fastq wolf/reads1
+		obi import --quality-solexa wolf_tutorial/wolf_F.fastq.gz wolf/reads1
 
 	`--quality-solexa` is the appropriate fastq quality option because it's an old dataset, `wolf_tutorial/wolf_F.fastq` is the path to the file to import, `wolf` is the path to the DMS that will be automatically created, and `reads1` is the name of the view into which the file will be imported.
 
 2. Import the second set of reads:
 
-		obi import --quality-solexa wolf_tutorial/wolf_R.fastq wolf/reads2
+		obi import --quality-solexa wolf_tutorial/wolf_R.fastq.gz wolf/reads2
 
 3. Import the [ngsfilter file](https://pythonhosted.org/OBITools/scripts/ngsfilter.html) describing the primers and tags used for each sample: