diff --git a/README.md b/README.md
index e818413b329e207ce925efada17b75dd4815bc18..84b8c845eb218f63ef4c4ea64743c859067aa07c 100644
--- a/README.md
+++ b/README.md
@@ -1,6 +1,6 @@
-<p align="left" width="100%", style="float">
-    <img width="15%" align="left" src=images/zarp_logo.svg>
-</p> 
+<div align="left">
+    <img width="20%" align="left" src=images/zarp_logo.svg>
+</div> 
 
 **ZARP** ([Zavolan-Lab][zavolan-lab] Automated RNA-Seq Pipeline) is a generic RNA-Seq analysis workflow that allows 
 users to process and analyze Illumina short-read sequencing libraries with minimum effort. The workflow relies on 
@@ -9,17 +9,17 @@ The workflow is developed in [Snakemake][snakemake], a widely used workflow mana
 community.
 
 According to the current ZARP implementation, reads are analyzed (pre-processed, aligned, quantified) with state-of-the-art
-tools to give meaningful initial insights into the quality and composition of an RNA-Seq library, reducing hands-on time for bioinformaticians and giving experimentalists the possibility to rapidly assess their data. 
-
-Additional reports summarise the results of the individual steps and provide useful visualisations.
-For a more detailed description of each step, please refer to the [workflow
-documentation][pipeline-documentation].
+tools to give meaningful initial insights into the quality and composition of an RNA-Seq library, reducing hands-on time for bioinformaticians and giving experimentalists the possibility to rapidly assess their data. Additional reports summarise the results of the individual steps and provide useful visualisations.
 
 <div align="center">
-    <img width="60%" align="center" src=images/zarp_schema.png>
+    <img width="60%" src=images/zarp_schema.png>
 </div> 
 
 
+> **Note:** For a more detailed description of each step, please refer to the [workflow
+> documentation][pipeline-documentation].
+
+
 # Requirements
 
 The workflow has been tested on: