Update readme for version 2.0.2

README.md

@@ -2,8 +2,19 @@
 Cancer immunotherapy has gained significant momentum from recent clinical successes of checkpoint blockade inhibition. Massively parallel sequence analysis suggests a connection between mutational load and response to this class of therapy. Methods to identify which tumor-specific mutant peptides (neoantigens) can elicit anti-tumor T cell immunity are needed to improve predictions of checkpoint therapy response and to identify targets for vaccines and adoptive T cell therapies. Here, we provide a cancer immunotherapy pipeline for the identification of **p**ersonalized **V**ariant **A**ntigens by **C**ancer **Seq**uencing (pVAC-Seq) that integrates tumor mutation and expression data (DNA- and RNA-Seq).
 http://www.genomemedicine.com/content/8/1/11
 
+## New in version 2.0.2
+<ul>
+<li>Bugfix: There was a problem in version 2.0.1 where pVAC-Seq would hang while calling NetMHC under certain cirumstances. This is now fixed.</li>
+<li>Bugfix: When using multiple alleles or epitope lengths, pVAC-Seq would not output all candidate epitopes after running the binding filter. This has now been fixed.</li>
+</ul>
+
 ## New in version 2.0.1
 <ul>
+<li>Silence output from NetMHC</li>
+</ul>
+
+## New in version 2.0.0
+<ul>
 <li>Supports inframe indels and frameshifts.</li>
 <li>Supports VCF as the input file format.</li>
 </ul>