diff --git a/README.md b/README.md
index c886d32..73808aa 100644
--- a/README.md
+++ b/README.md
@@ -1,4 +1,4 @@
-[![Downloads](https://img.shields.io/github/downloads/Nextomics/NextPolish/total.svg)](https://github.com/Nextomics/NextPolish/releases/download/V1.0.0/NextPolish.tgz)
+[![Downloads](https://img.shields.io/github/downloads/Nextomics/NextPolish/total.svg)](https://github.com/Nextomics/NextPolish/releases/download/v1.0.0/NextPolish.tgz)
 [![Release](https://img.shields.io/github/release/Nextomics/NextPolish.svg)](https://github.com/Nextomics/NextPolish/releases)
 [![Last-commit](https://img.shields.io/github/last-commit/Nextomics/NextPolish.svg)](https://github.com/Nextomics/NextPolish/commits/master)
 [![Issues](https://img.shields.io/github/issues/Nextomics/NextPolish.svg)](https://github.com/Nextomics/NextPolish/issues)
@@ -7,8 +7,8 @@
 NextPolish is used to fix base errors (SNP/Indel) in the genome generated by noisy long reads, it can be used with short read data only or long read data only or a combination of both. It contains two core modules and four steps (steps 3 & 4 are optional), and use a stepwise fashion to correct the error bases in reference genome. To correct the raw TGS long reads with approximately 15-10% sequencing errors, please use [NextDenovo](https://github.com/Nextomics/NextDenovo).
 
 * **DOWNLOAD**  
-click [here](https://github.com/Nextomics/NextPolish/releases/download/V1.0.0/NextPolish.tgz) or use the following command:  
-`wget https://github.com/Nextomics/NextPolish/releases/download/V1.0.0/NextPolish.tgz`  
+click [here](https://github.com/Nextomics/NextPolish/releases/download/v1.0.0/NextPolish.tgz) or use the following command:  
+`wget https://github.com/Nextomics/NextPolish/releases/download/v1.0.0/NextPolish.tgz`  
 
 * **REQUIREMENT**
 	* [Python 2.7](https://www.python.org/download/releases/2.7/)