Added variant calling link

README.md

@@ -218,12 +218,12 @@ See our current workshop schedule on our [training website](http://bioinformatic
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     <td><b>C</b> - Analysis of HTS data in the HPC environment</td>
     <td>Anyone planning on doing genomic or transcriptomic next-generation sequencing and is interested in analyzing their own data.</td>
-    <td> - Analysis of bulk RNAseq data, Variant calling, and sequencing data related to Chromatin biology starting with raw data.<br><br>
+    <td> - Analysis of bulk RNAseq data, Variant Analysis, and sequencing data related to Chromatin biology starting with raw data.<br><br>
       - Automating the workflow with advanced shell scripts.</td>
     <td><ul><li><a href="https://hbctraining.github.io/Intro-to-rnaseq-hpc-salmon-flipped/">Introduction to (bulk) RNA-seq using High-Performance Computing - O2 cluster</a></li>
       <li><a href="https://hbctraining.github.io/Intro-to-rnaseq-fasrc-salmon-flipped/">Introduction to (bulk) RNA-seq using High-Performance Computing - FAS-RC cluster</a></li>
       <li><a href="https://hbctraining.github.io/Intro-to-ChIPseq-flipped/">Understanding chromatin biology using high throughput sequencing</a></li>
-      <li><a href="">Variant calling</a></li></ul></td>
+      <li><a href="https://hbctraining.github.io/variant_analysis/">Variant Analysis</a></li></ul></td>
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     <td><b>D</b> - Statistical Analysis of HTS data in R</td>