diff --git a/docs/tutorials/tutorial-1.rst b/docs/tutorials/tutorial-1.rst
index dc0aaf0..d514202 100644
--- a/docs/tutorials/tutorial-1.rst
+++ b/docs/tutorials/tutorial-1.rst
@@ -485,7 +485,7 @@ There are many, many other assembly QC steps you can run other than simply
 looking at the stats of the assembled contigs.  We will not go into those here.
 
 
-.. _FindingUCELoci:
+.. _finding-uce-loci:
 
 Finding UCE loci
 ================
diff --git a/docs/tutorials/tutorial-3.rst b/docs/tutorials/tutorial-3.rst
index ab4ca4e..e088849 100644
--- a/docs/tutorials/tutorial-3.rst
+++ b/docs/tutorials/tutorial-3.rst
@@ -402,8 +402,8 @@ The easiest way for you to use the extracted sequences is to basically pretend
 like they are "newly assembled contigs" and place the fasta files (`allmis2.fasta` 
 as in the above) into a `contigs` directory.  Alternatively, you can symlink them 
 into a new or existing `contigs` folder (that resulted from a PHYLUCE_ assembly 
-process) and then proceed with the :ref:`FindingUCELoci` procedure.
+process) and then proceed with the :ref:`finding-uce-loci` procedure.
 
  .. attention:: Although we have already extracted the UCE loci from each genome
     sequence and even though it seems redundant to go back through the
-    :ref:`FindingUCELoci` process, this is the best path forward.
+    :ref:`finding-uce-loci` process, this is the best path forward.