diff --git a/README.md b/README.md
index 48fd58112ce37cf13e9ef77fe79bc52e6188bf63..80f0de11eb15b01c0b06b2ecf41086fdb27521e9 100644
--- a/README.md
+++ b/README.md
@@ -3,7 +3,7 @@ DISCO-Digital Microfluidic Isolation of Single Cells for - Omics.
 The laser lysis capture method implemented in DISCO offers spatially and temporally resolved capture of single cells, while Digital Microfluidics (DMF) is capable of retrieving this lysate and permitting flexible downstream analyses, such as scRNA-seq.
 Each cell has a barcode incorporated into Read 1, making the cell's transcriptome accountable and traceable throughout the pipeline. This barcode includes a unique cell barcode (12bp) and a UMI (8bp). The first part of our bioinformatic pipeline deals with parsing these.
 
-## General Worlflow
+## General Workflow
 The provided scripts go through mapping, parsing fasta headers (barcodes and UMIs), generating count data, making figures and performing differential gene expression (DGE):
 1. Append Read1 barcode information to Read2 fasta header 
 2. Align with Star Aligner