diff --git a/content/authors/SeqImprove/_index.md b/content/authors/SeqImprove/_index.md
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+---
+# Display name
+title: SeqImprove
+
+#Use 1 for PI, 100 for Current Postdocs, 200 for current phds, 300 for current masters, 400 for current undergrads, 800 for alum postdocs, 810 for alum phds, 820 for alum masters, and 830 for alum undergrads, 900 for tools, 1000 for projects, 900 for tools, 1000 for projects
+weight: 900
+
+# Username (this should match the folder name)
+authors:
+- SeqImprove
+
+#Author Names (alternative spellings etc)
+names:
+- SeqImprove
+
+#Link to this when clicking on tool icons
+toolurl: https://seqimprove.synbiohub.org
+
+# Is this the primary user of the site?
+superuser: false
+
+projects:
+- SeqImprove is a web tool that automatically annotates sequence information using part libraries and exports SBOL output.
+
+# Short bio (displayed in user profile at end of posts)
+# bio: My research interests include distributed robotics, mobile computing and programmable matter.
+
+# Social/Academic Networking
+# For available icons, see: https://sourcethemes.com/academic/docs/page-builder/#icons
+#   For an email link, use "fas" icon pack, "envelope" icon, and a link in the
+#   form "mailto:your-email@example.com" or "#contact" for contact widget.
+social:
+- icon: star
+  icon_pack: fas
+  link: https://seqimprove.synbiohub.org
+# - icon: docker
+#   icon_pack: fab
+#   link: https://hub.docker.com/r/paytonco/ibiosim
+- icon: github
+  icon_pack: fab
+  link: https://github.com/MyersResearchGroup/SeqImprove
+
+# Organizational groups that you belong to (for People widget)
+#   Set this to `[]` or comment out if you are not using People widget.
+user_groups:
+- Tools
+- Genetic Design Automation
+- SeqImprove
+
+#any user groups to display on the page
+display_groups:
+- SeqImprove
+
+research_area: true
+
+research_area_tags:
+- SeqImprove
+---
+
+SeqImprove was designed to fill a need identified for ad hoc curation by synthetic biologists prior to publishing their work, in order to ensure that their data is findable, accessible, interoperable, and reusable (FAIR). It offers an easy way to apply SBOL annotations to sequence data without requiring that the user have an intimate understanding of SBOL's technical specifications. 
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