diff --git a/haplotagdata.md b/haplotagdata.md
index 9739a28ea..ec224189e 100644
--- a/haplotagdata.md
+++ b/haplotagdata.md
@@ -50,7 +50,7 @@ sequences, then it will make sure the `BX:Z:` tag is moved to the end of the ali
 !!!
 
 ### Read length
-Reads must be at least 30 base pairs in length for alignment. The `trim` module removes reads <50bp.
+Reads must be at least 30 base pairs in length for alignment. The `qc` module removes reads <50bp.
 
 ### Compression
 Harpy generally doesn't require the input sequences to be in gzipped/bgzipped format, but it's good practice to compress your reads anyway.
@@ -60,7 +60,7 @@ Compressed files are expected to end with the extension `.gz`.
 Unfortunately, there are many different ways of naming FASTQ files, which makes it 
 difficult to accomodate every wacky iteration currently in circulation.
 While Harpy tries its best to be flexible, there are limitations. 
-To that end, for the `demultiplex`, `trim`, and `align` modules, the 
+To that end, for the `demultiplex`, `qc`, and `align` modules, the 
 most common FASTQ naming styles are supported:
 - **sample names**: Alphanumeric and `.`, `-`, `_`
     - you can mix and match special characters, but that's bad practice and not recommended
diff --git a/snakemake.md b/snakemake.md
index fe3cd7afb..065da352e 100644
--- a/snakemake.md
+++ b/snakemake.md
@@ -49,7 +49,7 @@ Sometimes you want to generate a specific intermediate file (or files) rather th
 you want the beadtag report Harpy makes from the output of `EMA count`. To do this, just list the file/files (relative
 to your working directory) without any flags. Example for the beadtag report:
 ```bash
-harpy align -g genome.fasta -d Trim/ -t 4 -s "Align/ema/stats/reads.bxstats.html"
+harpy align -g genome.fasta -d QC/ -t 4 -s "Align/ema/stats/reads.bxstats.html"
 ```
 This of course necessitates knowing the names of the files ahead of time. See the individual modules for a breakdown of expected outputs.