Join us at ESHG 2025 and learn how MGI commits in advancing clinical and population genomics
4/24/25
4/27/25
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Milan, Italy
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MGI Corporate Session: Advancing Clinical and Population Genomics with MGI’s DNBSEQ and Multi-Omics Solutions
Join our must-attend session featuring real-world research in oncology and national genomics - showcasing how integrated approaches and DNBSEQ™ technology are advancing clinical genomics and personalized healthcare.
🕓 Saturday 24 May, 12:15 - 13:30 CET
📍 Room Amber 7 + 8
🍴 Lunch will be provided
REGISTER HERE
Agenda:
Building a National Genomic Infrastructure as Part of the European 1+ Million Genomes Initiative: Whole-Genome Sequencing for Population Reference and Clinical Applications. Prof. Janis Klovins, Professor & Head of the Scientific Council, Latvian Biomedical Research & Study Centre, Latvia
The Clinical Utility of Multigene Panel Analysis in Precision Oncology. Dr. Eirini Papadopoulou, International Laboratory Director, Genekor Medical S.A, Greece
Decode Half Million Genomes in Half Year: Insights from the China Kadoorie Biobank (CKB). Dr. Xin Jin, Chief Scientist & Director of the Institute of Precision Health Research at BGl-Research, China
Introducing Our Next Innovations
Live at Booth #310
Explore the DNBSEQ-T1+, DNBSEQ-G99, DNBSEQ-T7, DNBSEQ-T20x2 & Stereo-Seq spatial platforms - and speak with our experts to learn how our multi-omics solutions can advance your research.
Join us as we unveil the future of single-cell library prep - 24 May | 16:10 | Booth #310
Featured Talks and Posters at ESHG 2025
Unveiling spatial heterogeneity in medulloblastoma: a multi-omics analysis of cellular state and geographicalorganization. Dr. Li Jiankang, Session: C19-CancerComplexity: Variants,Therapies and AI-Driven Insights, Sunday, May 25
Artificial intelligence allows accurate fetal genome deduction and noninvasive prenatal diagnosis of single gene diseases and copy number variants in fetus. Dr. Ya Gao, Session: C21 - Prenatal and reproductive medicine, Sunday, May 25
Early prediction of preterm birth with cell-free RNA. Dr. Ji Yi, E-poster, at Exhibition Hall
Middle-read sequencing: bridging the gap between short-read and long-read sequencing with superior performance and cost efficiency. Dr. Heng Yi, E-poster, at Exhibition Hall
MGI Corporate Session: Advancing Clinical and Population Genomics with MGI’s DNBSEQ and Multi-Omics Solutions
Join our must-attend session featuring real-world research in oncology and national genomics - showcasing how integrated approaches and DNBSEQ™ technology are advancing clinical genomics and personalized healthcare.
🕓 Saturday 24 May, 12:15 - 13:30 CET
📍 Room Amber 7 + 8
🍴 Lunch will be provided
REGISTER HERE
Agenda:
Building a National Genomic Infrastructure as Part of the European 1+ Million Genomes Initiative: Whole-Genome Sequencing for Population Reference and Clinical Applications. Prof. Janis Klovins, Professor & Head of the Scientific Council, Latvian Biomedical Research & Study Centre, Latvia
The Clinical Utility of Multigene Panel Analysis in Precision Oncology. Dr. Eirini Papadopoulou, International Laboratory Director, Genekor Medical S.A, Greece
Decode Half Million Genomes in Half Year: Insights from the China Kadoorie Biobank (CKB). Dr. Xin Jin, Chief Scientist & Director of the Institute of Precision Health Research at BGl-Research, China
Introducing Our Next Innovations
Live at Booth #310
Explore the DNBSEQ-T1+, DNBSEQ-G99, DNBSEQ-T7, DNBSEQ-T20x2 & Stereo-Seq spatial platforms - and speak with our experts to learn how our multi-omics solutions can advance your research.
Join us as we unveil the future of single-cell library prep - 24 May | 16:10 | Booth #310
Featured Talks and Posters at ESHG 2025
Unveiling spatial heterogeneity in medulloblastoma: a multi-omics analysis of cellular state and geographicalorganization. Dr. Li Jiankang, Session: C19-CancerComplexity: Variants,Therapies and AI-Driven Insights, Sunday, May 25
Artificial intelligence allows accurate fetal genome deduction and noninvasive prenatal diagnosis of single gene diseases and copy number variants in fetus. Dr. Ya Gao, Session: C21 - Prenatal and reproductive medicine, Sunday, May 25
Early prediction of preterm birth with cell-free RNA. Dr. Ji Yi, E-poster, at Exhibition Hall
Middle-read sequencing: bridging the gap between short-read and long-read sequencing with superior performance and cost efficiency. Dr. Heng Yi, E-poster, at Exhibition Hall
MGI Corporate Session: Advancing Clinical and Population Genomics with MGI’s DNBSEQ and Multi-Omics Solutions
Join our must-attend session featuring real-world research in oncology and national genomics - showcasing how integrated approaches and DNBSEQ™ technology are advancing clinical genomics and personalized healthcare.
🕓 Saturday 24 May, 12:15 - 13:30 CET
📍 Room Amber 7 + 8
🍴 Lunch will be provided
REGISTER HERE
Agenda:
Building a National Genomic Infrastructure as Part of the European 1+ Million Genomes Initiative: Whole-Genome Sequencing for Population Reference and Clinical Applications. Prof. Janis Klovins, Professor & Head of the Scientific Council, Latvian Biomedical Research & Study Centre, Latvia
The Clinical Utility of Multigene Panel Analysis in Precision Oncology. Dr. Eirini Papadopoulou, International Laboratory Director, Genekor Medical S.A, Greece
Decode Half Million Genomes in Half Year: Insights from the China Kadoorie Biobank (CKB). Dr. Xin Jin, Chief Scientist & Director of the Institute of Precision Health Research at BGl-Research, China
Introducing Our Next Innovations
Live at Booth #310
Explore the DNBSEQ-T1+, DNBSEQ-G99, DNBSEQ-T7, DNBSEQ-T20x2 & Stereo-Seq spatial platforms - and speak with our experts to learn how our multi-omics solutions can advance your research.
Join us as we unveil the future of single-cell library prep - 24 May | 16:10 | Booth #310
Featured Talks and Posters at ESHG 2025
Unveiling spatial heterogeneity in medulloblastoma: a multi-omics analysis of cellular state and geographicalorganization. Dr. Li Jiankang, Session: C19-CancerComplexity: Variants,Therapies and AI-Driven Insights, Sunday, May 25
Artificial intelligence allows accurate fetal genome deduction and noninvasive prenatal diagnosis of single gene diseases and copy number variants in fetus. Dr. Ya Gao, Session: C21 - Prenatal and reproductive medicine, Sunday, May 25
Early prediction of preterm birth with cell-free RNA. Dr. Ji Yi, E-poster, at Exhibition Hall
Middle-read sequencing: bridging the gap between short-read and long-read sequencing with superior performance and cost efficiency. Dr. Heng Yi, E-poster, at Exhibition Hall
MGI Corporate Session: Advancing Clinical and Population Genomics with MGI’s DNBSEQ and Multi-Omics Solutions
Join our must-attend session featuring real-world research in oncology and national genomics - showcasing how integrated approaches and DNBSEQ™ technology are advancing clinical genomics and personalized healthcare.
🕓 Saturday 24 May, 12:15 - 13:30 CET
📍 Room Amber 7 + 8
🍴 Lunch will be provided
REGISTER HERE
Agenda:
Building a National Genomic Infrastructure as Part of the European 1+ Million Genomes Initiative: Whole-Genome Sequencing for Population Reference and Clinical Applications. Prof. Janis Klovins, Professor & Head of the Scientific Council, Latvian Biomedical Research & Study Centre, Latvia
The Clinical Utility of Multigene Panel Analysis in Precision Oncology. Dr. Eirini Papadopoulou, International Laboratory Director, Genekor Medical S.A, Greece
Decode Half Million Genomes in Half Year: Insights from the China Kadoorie Biobank (CKB). Dr. Xin Jin, Chief Scientist & Director of the Institute of Precision Health Research at BGl-Research, China
Introducing Our Next Innovations
Live at Booth #310
Explore the DNBSEQ-T1+, DNBSEQ-G99, DNBSEQ-T7, DNBSEQ-T20x2 & Stereo-Seq spatial platforms - and speak with our experts to learn how our multi-omics solutions can advance your research.
Join us as we unveil the future of single-cell library prep - 24 May | 16:10 | Booth #310
Featured Talks and Posters at ESHG 2025
Unveiling spatial heterogeneity in medulloblastoma: a multi-omics analysis of cellular state and geographicalorganization. Dr. Li Jiankang, Session: C19-CancerComplexity: Variants,Therapies and AI-Driven Insights, Sunday, May 25
Artificial intelligence allows accurate fetal genome deduction and noninvasive prenatal diagnosis of single gene diseases and copy number variants in fetus. Dr. Ya Gao, Session: C21 - Prenatal and reproductive medicine, Sunday, May 25
Early prediction of preterm birth with cell-free RNA. Dr. Ji Yi, E-poster, at Exhibition Hall
Middle-read sequencing: bridging the gap between short-read and long-read sequencing with superior performance and cost efficiency. Dr. Heng Yi, E-poster, at Exhibition Hall
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May 20, 2025
Join us at SLAS Europe 2025 and discover our latest innovation
Join us at booth #516 and discover how we're driving innovation in labs. Don’t miss this opportunity to engage with our team, explore our latest technologies, and be part of the conversation shaping the future of life sciences.
Mar 19, 2025
Join us at VIB Conference, from March 19 to 21 in Antwerp, Belgium!
Our team will be there to discuss how our technology can meet your needs and discover how MGI is making #OMICS accessible for all.
We look forward to connecting with you and exploring how we can revolutionize sequencing together!
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I have read and understood MGI’s Privacy Policy, and I consent to the collection and processing of my personal data for handling, responding to my contact, receiving your newsletter as well as promotion and marketing activities.
*For Research Use Only
Not for use in diagnostic procedures (except as specifically noted).
Join our newsletter to stay up to date on features and releases.
I have read and understood MGI’s Privacy Policy, and I consent to the collection and processing of my personal data for handling, responding to my contact, receiving your newsletter as well as promotion and marketing activities.
*For Research Use Only
Not for use in diagnostic procedures (except as specifically noted).
Join our newsletter to stay up to date on features and releases.
I have read and understood MGI’s Privacy Policy, and I consent to the collection and processing of my personal data for handling, responding to my contact, receiving your newsletter as well as promotion and marketing activities.
*For Research Use Only
Not for use in diagnostic procedures (except as specifically noted).