doc: add fulcrum genomics more prominently

Author: nh13

.github/logos/fulcrumgenomics.svg

@@ -7,9 +7,15 @@
   <a href="http://bioconda.github.io/recipes/guide-counter/README.html"><img src="https://img.shields.io/conda/dn/bioconda/guide-counter.svg?label=bioconda" alt="Bioconda"></a>
   <a href="https://doi.org/10.5281/zenodo.6375791"><img src="https://zenodo.org/badge/DOI/10.5281/zenodo.6375791.svg" alt="DOI"></a>
   <br>
-  A better, faster way to count guides in CRISPR screens.
 </p>
 
+A better, faster way to count guides in CRISPR screens.
+
+[Visit us at Fulcrum Genomics](www.fulcrumgenomics.com) to learn more about how we can power your Bioinformatics with guide-counter and beyond.
+
+<a href="mailto:contact@fulcrumgenomics.com?subject=[GitHub inquiry]"><img src="https://img.shields.io/badge/Email_us-brightgreen.svg?&style=for-the-badge&logo=gmail&logoColor=white"/></a>
+<a href="https://www.fulcrumgenomics.com"><img src="https://img.shields.io/badge/Visit_Us-blue.svg?&style=for-the-badge&logo=wordpress&logoColor=white"/></a>
+
 ## Overview
 
 `guide-counter` is a tool for processing FASTQ files from CRISPR screen experiments to generate a matrix of per-sample guide counts.  It can be used as a faster, more accurate, drop in replacement for `mageck count`.  By default `guide-counter` will look for guide seqeunces in the reads with 0 or 1 mismatches vs. the expected guides, but can be run in exact matching mode.