enGenome among start-up champions to receive funding from European Innovation Council Accelerator
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News
enGenome’s Run for Rare to raise awareness for Rare Disease Day
29 February 2024
Articles
Rare diseases: an overwhelming economic scenario
28 February 2024
Events
enGenome gets ready for the Festival of Genomics in London
17 January 2024
Events
enGenome takes the stage at PMWC in Silicon Valley
17 January 2024
Events
enGenome heads to Paris for Assises de Génétique Humaine et Médicale in 2024!
4 January 2024
Events
enGenome will attend CIGH 2023 in Málaga, Spain
8 November 2023
News
enGenome launches VarChat: the first GenAI genomic variant assistant
2 November 2023
Webinar
eVai: Mastering Variant Interpretation in Diagnostics
12 October 2023
Events
enGenome presenting at SIGU 2023 in Rimini, Italy
20 September 2023
Events
enGenome invited to teach at PhD Week Course
7 September 2023
Events
enGenome's acceptance for a platform oral presentation at the ASHG in Washington, DC
31 August 2023
Articles
Artificial Intelligence regulation and the future of clinical genomics
19 July 2023
News
eVai now performs detection and interpretation of mitochondrial DNA variants!
12 July 2023
News
enGenome supports Williams Syndrome Association by sponsoring a fundraiser Golf Tournament in New England, United States.
26 June 2023
Events
enGenome at Grandangolo 2023 in Rome
19 May 2023
Articles
Mitochondrial DNA: the code powering the cell energy
18 May 2023
Events
ESHG 2023: enGenome to show AI-based variant interpretation at Corporate Satellite
10 May 2023
Articles
From HGP to T2T: the foundation for a new genomic era
28 March 2023
Events
enGenome at GfH 2023 in Kassel, Germany
7 March 2023
Events
enGenome at ACMG 2023 in Salt Lake City
7 March 2023
News
“We Care About Rare”: enGenome’s new campaign on Rare Disease
28 February 2023
Articles
The Diagnostic Odyssey of rare diseases: the impact of an early and accurate diagnosis.
20 February 2023
News
eVai is now fully equipped to perform variant interpretation seamlessly from FastQ!
10 February 2023
Webinar
Suggested Diagnosis: where machine-learning meets variant prioritization
18 November 2022
News
Bando Brevetti 2021
7 November 2022
Events
enGenome at ASHG 2022 in Los Angeles
14 October 2022
Events
enGenome at SIGU 2022 in Trieste
5 September 2022
News
Concessioni di contributi/finanziamenti pubblici
31 July 2022
Events
ESHG 2022: enGenome Solutions for Excellence in Variant Interpretation
27 May 2022
News
enGenome’s eVai platform is a best performer in the NIH-funded CAGI6 Challenge
24 May 2022
Events
enGenome at Grandangolo Roma 2022
4 March 2022
News
Rare Disease Day 2022: Marfan Syndrome
28 February 2022
News
Rare Disease Day 2022: explaining RD to young children
25 February 2022
Success stories
S.Matteo Hospital – Hematology Oncology
26 November 2021
Events
enGenome at SIGU 2021 Virtual Meeting
15 November 2021
News
enGenome among start-up champions to receive funding from European Innovation Council Accelerator
14 October 2021
Events
enGenome at ASHG 2021 Virtual Meeting
6 October 2021
Articles
Digenic inheritance: a key mechanism for understanding rare diseases
27 August 2021
Events
ESHG 2021: Enhance your NGS variant analysis
24 August 2021
Articles
Rapid WGS: the impact on newborns
30 June 2021
Articles
Deep Intronic Mutations and Human Diseases
18 June 2021
Articles
WES and WGS, a comparison of usage
10 May 2021
Articles
The HPO: the importance of clinical coding in variant interpretation
2 April 2021
News
enGenome and Unimib for Scientific Content Creator Project
26 March 2021
Webinar
Diagnostica oncologica e CNV: il workflow di analisi dati NGS
12 March 2021
Articles
The right diagnosis is the first step to fight the Rare Disease battle
27 February 2021
Webinar
Bench to bedside: successful application of WES in the molecular diagnosis of genetic diseases
14 January 2021
Articles
Copy Number Variations: beyond discovery
20 December 2020
Events
Business Forum Canada-Italy on AI
13 November 2020
Success stories
Medical College of Wisconsin
21 October 2020
Success stories
University of Pavia – Biotechnology Department
10 September 2020
Webinar
Gene Constraint Webinar
28 August 2020
Articles
The Digital Genomic Era
5 August 2020
Quality
eVai has qualified as an AgID certified supplier
3 August 2020
Success stories
Enabling accurate and fast variant analysis for the diagnosis of genetic diseases causing hearing loss
14 July 2020
Quality
Consensus Assessment Initiative Questionnaire
20 May 2020
Webinar
eVai Webinar
20 May 2020
Success stories
The benefits of hypothesis-free interpretation to solve undiagnosed cases
23 December 2019
Events
enGenome at the SIGU 2019 in Rome
30 October 2019
Articles
Tackling the bottleneck of Variant Interpretation
11 October 2019
Events
enGenome at the ASHG 2019 in Houston
8 August 2019
Success stories
Lung and colorectal cancer variant prioritization at Kabara Cancer Research Institute
29 July 2019
Articles
The powerful ways Artificial Intelligence is reshaping the diagnosis of genetic disorders
1 July 2019
Events
enGenome at ESHG 2019 in Gothenburg
15 June 2019
News
enGenome won G-factor Life Science Call
28 February 2019
Events
enGenome at ESHG 2018 in Milan
10 June 2018
Events
enGenome at SIGU 2017 in Naples
7 November 2017
News
enGenome won Novartis Oncology award
1 April 2017