From 301e4eb44ba217afb35bc22e132571378ef99e92 Mon Sep 17 00:00:00 2001
From: David Lougheed <david.lougheed@gmail.com>
Date: Thu, 21 Sep 2023 12:35:32 -0400
Subject: [PATCH] docs: add snv incorp as a feature

---
 README.md | 2 ++
 1 file changed, 2 insertions(+)

diff --git a/README.md b/README.md
index 5b1e96a..29cac5e 100644
--- a/README.md
+++ b/README.md
@@ -55,6 +55,8 @@ long read data should still work.
   catalog of TR loci and motifs.
 * Re-weighting of longer reads, to compensate for their lower likelihood of observation.
   * Whole-genome and targeted genotyping modes to adjust this re-weighting.
+* Incorporation of single-nucleotide variation (SNVs) for better and faster calling plus 
+  additional downstream analysis possibilities.
 * Parallelized for faster computing on clusters and for ad-hoc fast analysis of single samples.
 * 95% confidence intervals on calls via a user-configurable optional parametric bootstrapping process.