Impact of Genomic Variation on Function
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igvfconsortium.bsky.social
Impact of Genomic Variation on Function
@igvfconsortium.bsky.social
We're proud to recognize this year’s IGVF Team Science Award winners, leaders and teams whose work strengthens the entire consortium.

Congratulations to each of our award recipients 👏🏽
December 3, 2025 at 7:31 PM
Feeling extra grateful this November for the IGVF community!

Thank you for your collaboration, dedication, and the incredible work you do to advance our understanding of human health and disease.
November 26, 2025 at 6:26 PM
Wishing everyone a spook-tacular Halloween! 👻

Whether you’re celebrating or just enjoying a well-earned weekend, we hope it’s a wickedly wonderful one!
October 31, 2025 at 4:10 PM
From all fields and corners of the map, IGVF members came together in Durham, NC. United by one mission, to understand how genomic variation influences function.

A huge thank you to the Durham Bulls Athletic Park for welcoming us and hosting a fantastic night of food, fun, and practice home runs! ⚾
October 22, 2025 at 4:58 PM
We're live at #ASHG2025!

IGVF members are presenting across multiple sessions this week.

Check out where to find us and come say hi in Boston! 👋🏽
October 14, 2025 at 4:27 PM
#ASHG2025 kicks off next week!

Keep an eye out for IGVF presentations and posters throughout the meeting.

See you in Boston!
October 8, 2025 at 7:21 PM
ASHG 2025 is coming up! 🎉

Keep an eye out for IGVF talks and posters throughout the meeting.

We'll see you in Boston!
September 25, 2025 at 8:22 PM
The IGVF Consortium began with one mission: to understand how genomic variation shapes genome function and influences health. Together, we’re building lasting resources for the research community.

igvf.org
September 17, 2025 at 7:01 PM
IGVF uses state-of-the-art experimental and computational approaches to model, predict, characterize, and map genome function.

Together, these efforts are building a catalog that reveals how genomic variation influences genome function and phenotypes.
September 11, 2025 at 3:41 PM
Thousands of genomic variants are linked to disease, but how do they actually function?

IGVF is building a catalog of experimental and computational insights to uncover the impact of variants.

🔎 We’re on the case: igvf.org
August 6, 2025 at 3:24 PM
IGVF is uncovering how genomic variation impacts genome function and phenotype through mapping, modeling, and resource generation to advance research across the community.

Learn more: igvf.org
June 18, 2025 at 7:50 PM
Catch up on the latest research from the IGVF Catalog Working Group during our upcoming Knowledge Portal Webinar, featuring Michael Love, PhD.

Tune in Thursday, June 12th from 12–1 PM ET.

Details: hugeamp.org/news.html?ni...
June 11, 2025 at 4:10 PM
This upcoming #WorldEnvironmentDay, we reflect on how IGVF’s mission supports a more sustainable future.

By enabling more precise, efficient healthcare, we can reduce waste, streamline treatments, and advance environmental responsibility in biomedicine. 🌱🌍
June 3, 2025 at 3:48 PM
IGVF is advancing our understanding of how genomic variation affects genome function to influence phenotypes.

1️⃣ study, 1️⃣ collaboration, 1️⃣ discovery at a time.
May 28, 2025 at 1:33 PM
IGVF includes 5️⃣ core components.

Predictive Modeling, Characterization, Networking, Mapping, and Data Coordination.

Research teams across these groups work together to uncover how genomic variants influence genome function and phenotype.

Learn more: igvf.org/about/
April 25, 2025 at 5:32 PM
Our program goals are what drives the research.

IGVF is building a public catalog of variant impacts, advancing research across biology and medicine by combining data, tools, and models to better understand how genomic variation influences genome function and phenotypes.
April 10, 2025 at 5:14 PM
Collaboration is how we establish and conquer our common goals. April 1-4 in Cambridge, MA, we’re coming together to advance the GA4GH Road Map and shape the future of genomics.

We look forward to next week and to fostering partnerships and advancing common goals. 🎉
March 27, 2025 at 5:54 PM
🗓️ The deadline to register for in-person attendance at GA4GH Connect is Wednesday, March 18!

Join us April 1-4 in Cambridge, MA to collaborate, share insights, and help shape the future of the GA4GH Roadmap. We’ll see you there!

broadinstitute.swoogo.com/connect25bos/
March 13, 2025 at 4:13 PM
GA4GH April Connect 2025 is 31 days away!

April 1–4 in Cambridge, MA, join IGVF along with the GA4GH community in our common goal of advancing the GA4GH Road Map and shaping future developments.

In-person registration closes on March 18!

broadinstitute.swoogo.com/connect25bos...
February 28, 2025 at 8:03 PM
IGVF is advancing genomic research by developing a framework to understand how genetic variation affects genome function and shapes phenotypes.

This fundamental work lays the foundation for new discoveries in health and disease.
February 14, 2025 at 6:55 PM
IGVF is driving innovation by developing and testing predictive models to understand how genomic variation impacts genome function.

These crucial breakthroughs bring us closer to unraveling the complexities of human biology.

Learn more about our goals: igvf.org
January 17, 2025 at 8:32 PM
Another year in the books! 🗓️

IGVF wishes everyone a joyous start to 2025! 🎉

As we roll into a new month in a new year, we look forward to continued collaboration, innovation, and progress in genomic variation research.

#happynewyear
December 31, 2024 at 4:56 PM
IGVF aims to advance a network-level understanding of how genetic variation affects genome function and shapes phenotypes.

By leveraging research and collaboration, our ultimate goal is to create a comprehensive catalog of genomic variants and their impact on genome function and phenotypes.
December 10, 2024 at 7:52 PM
We’re excited to share the EUGENe toolkit—a powerful Python tool for building and evaluating sequence-based deep learning models in genomics! 🧬
EUGENe streamlines data management, model training, and prediction interpretation, making it easier to analyze biological sequences.
November 21, 2024 at 4:41 PM