News
enGenome among start-up champions to receive funding from European Innovation Council Accelerator
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Certification
enGenome Achieves ISO/IEC 27001:2022 Certification for Information Security, Cybersecurity and Privacy Protection
4 July 2024
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Articles
Unveiling the stigma of genetic discrimination
12 June 2024
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Events
enGenome at ESHG 2024 to present Corporate Satellite with guest from Twist Bioscience
20 May 2024
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Certification
Commitment to Excellence: enGenome's Quality Policy
20 May 2024
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Events
enGenome to showcase AI-driven solutions at ISV Conference in Porto, Portugal
6 May 2024
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Webinar
ESHG Sneak peek: Finding order in genomic disorders with enGenome’s AI
15 April 2024
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Events
enGenome invited to talk on AI to advance variant interpretation at HUGO 2024
28 March 2024
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News
enGenome’s Run for Rare to raise awareness for Rare Disease Day
29 February 2024
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Articles
Rare diseases: an overwhelming economic scenario
28 February 2024
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Events
enGenome gets ready for the Festival of Genomics in London
17 January 2024
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Events
enGenome takes the stage at PMWC in Silicon Valley
17 January 2024
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Events
enGenome heads to Paris for Assises de Génétique Humaine et Médicale in 2024!
4 January 2024
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Events
enGenome will attend CIGH 2023 in Málaga, Spain
8 November 2023
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News
enGenome launches VarChat: the first GenAI genomic variant assistant
2 November 2023
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Webinar
eVai: Mastering Variant Interpretation in Diagnostics
12 October 2023
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Events
enGenome presenting at SIGU 2023 in Rimini, Italy
20 September 2023
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Events
enGenome invited to teach at PhD Week Course
7 September 2023
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Events
enGenome's acceptance for a platform oral presentation at the ASHG in Washington, DC
31 August 2023
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Articles
Artificial Intelligence regulation and the future of clinical genomics
19 July 2023
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News
eVai now performs detection and interpretation of mitochondrial DNA variants!
12 July 2023
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News
enGenome supports Williams Syndrome Association by sponsoring a fundraiser Golf Tournament in New England, United States.
26 June 2023
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Events
enGenome at Grandangolo 2023 in Rome
19 May 2023
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Articles
Mitochondrial DNA: the code powering the cell energy
18 May 2023
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Events
ESHG 2023: enGenome to show AI-based variant interpretation at Corporate Satellite
10 May 2023
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Articles
From HGP to T2T: the foundation for a new genomic era
28 March 2023
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Events
enGenome at GfH 2023 in Kassel, Germany
7 March 2023
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Events
enGenome at ACMG 2023 in Salt Lake City
7 March 2023
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News
“We Care About Rare”: enGenome’s new campaign on Rare Disease
28 February 2023
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Articles
The Diagnostic Odyssey of rare diseases: the impact of an early and accurate diagnosis.
20 February 2023
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News
eVai is now fully equipped to perform variant interpretation seamlessly from FastQ!
10 February 2023
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Webinar
Suggested Diagnosis: where machine-learning meets variant prioritization
18 November 2022
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News
Bando Brevetti 2021
7 November 2022
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Events
enGenome at ASHG 2022 in Los Angeles
14 October 2022
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Events
enGenome at SIGU 2022 in Trieste
5 September 2022
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News
Concessioni di contributi/finanziamenti pubblici
31 July 2022
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Events
ESHG 2022: enGenome Solutions for Excellence in Variant Interpretation
27 May 2022
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News
enGenome’s eVai platform is a best performer in the NIH-funded CAGI6 Challenge
24 May 2022
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Events
enGenome at Grandangolo Roma 2022
4 March 2022
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News
Rare Disease Day 2022: Marfan Syndrome
28 February 2022
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News
Rare Disease Day 2022: explaining RD to young children
25 February 2022
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Success stories
S.Matteo Hospital – Hematology Oncology
26 November 2021
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Events
enGenome at SIGU 2021 Virtual Meeting
15 November 2021
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News
enGenome among start-up champions to receive funding from European Innovation Council Accelerator
14 October 2021
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Events
enGenome at ASHG 2021 Virtual Meeting
6 October 2021
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Articles
Digenic inheritance: a key mechanism for understanding rare diseases
27 August 2021
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Events
ESHG 2021: Enhance your NGS variant analysis
24 August 2021
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Articles
Rapid WGS: the impact on newborns
30 June 2021
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Articles
Deep Intronic Mutations and Human Diseases
18 June 2021
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Articles
WES and WGS, a comparison of usage
10 May 2021
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Articles
The HPO: the importance of clinical coding in variant interpretation
2 April 2021
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News
enGenome and Unimib for Scientific Content Creator Project
26 March 2021
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Webinar
Diagnostica oncologica e CNV: il workflow di analisi dati NGS
12 March 2021
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Articles
The right diagnosis is the first step to fight the Rare Disease battle
27 February 2021
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Webinar
Bench to bedside: successful application of WES in the molecular diagnosis of genetic diseases
14 January 2021
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Articles
Copy Number Variations: beyond discovery
20 December 2020
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Events
Business Forum Canada-Italy on AI
13 November 2020
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Success stories
Medical College of Wisconsin
21 October 2020
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Success stories
University of Pavia – Biotechnology Department
10 September 2020
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Webinar
Gene Constraint Webinar
28 August 2020
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Articles
The Digital Genomic Era
5 August 2020
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Certification
eVai has qualified as an AgID certified supplier
3 August 2020
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Success stories
Enabling accurate and fast variant analysis for the diagnosis of genetic diseases causing hearing loss
14 July 2020
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Certification
Consensus Assessment Initiative Questionnaire
20 May 2020
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Webinar
eVai Webinar
20 May 2020
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Success stories
The benefits of hypothesis-free interpretation to solve undiagnosed cases
23 December 2019
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Events
enGenome at the SIGU 2019 in Rome
30 October 2019
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Articles
Tackling the bottleneck of Variant Interpretation
11 October 2019
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Events
enGenome at the ASHG 2019 in Houston
8 August 2019
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Success stories
Lung and colorectal cancer variant prioritization at Kabara Cancer Research Institute
29 July 2019
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Articles
The powerful ways Artificial Intelligence is reshaping the diagnosis of genetic disorders
1 July 2019
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Events
enGenome at ESHG 2019 in Gothenburg
15 June 2019
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News
enGenome won G-factor Life Science Call
28 February 2019
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Events
enGenome at ESHG 2018 in Milan
10 June 2018
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Events
enGenome at SIGU 2017 in Naples
7 November 2017
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News
enGenome won Novartis Oncology award
1 April 2017