Events

„Genomic Intelligence“ – AI meets Genomics

In a virtual workshop on May 21, 2021 (11:00-15.00), we will explore the interest at our university to use AI to unravel genomic questions.

We are looking for contributions in form of either (1) availability of genomics data, ideally with specific challenges you wish to address, or (2) AI expertise that you would like to apply to genomics problems. Explicitly “newcomers” to genomics are welcome!

Please sign-up here: https://forms.gle/uA8bqQjHUjbeaTge6

 

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Jeanette Erdmann is invited to talk at the 2021 BCS Virtual Annual Conference

Jeanette Erdmann is invited to give a talk about “What have we learnt for coronary artery disease?” at the 2021 BCS Virtual Annual Conference held June 7-10, 2021.

Due to the ongoing COVID-19 pandemic this conference will be virtual. Faculty talks will be pre-recorded and the session Q&A’s will be live, taking place during the event.

More details can be found here: https://cutt.ly/JbkNZ5Z

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Jeanette Erdmann is invited to deliver a talk about “AI in genetics”

Jeanette Erdmann is invited to give a talk about “AI in genetics” at the Artificial Intelligence in Cardiovascular Disease meeting held May 26th-27th, 2021.

Due to the pandemic this meeting is planned as a hybrid meeting with live broadcasting.

Joining is possible either at the Cavendish Conference Centre in London or virtually.

More details can be found here: https://cutt.ly/2bkVgMV

Jeanette Erdmann is invited to deliver a talk about “AI in genetics” Read More »

Jeanette Erdmann is invited to talk about “DNA, RNA, Proteine – im Dschungel der Sequenzierungsanalysen”

Jeanette Erdmann is invited to give a talk about “DNA, RNA, Proteine – im Dschungel der Sequenzierungsmethoden” at the Young DGK #Science meeting held April 29, 2021 from 3:00-5:00 pm.

Due to the pandemic this meeting is online-only.

More details can be found here: https://cutt.ly/rbkBY0c

Jeanette Erdmann is invited to talk about “DNA, RNA, Proteine – im Dschungel der Sequenzierungsanalysen” Read More »

Lecture Series “Seltene Erkrankungen”

The Junior Members of the Society for Biochemistry and Molecular Biology (GBM), are organizing a lecture series on “Rare Diseases” in January and February 2021.
The Junior GBM are a small group of Molecular Life Science students who, since their foundation in 2013, have been organizing both internal and public events that are part of their interests in a scientific context and allow them to gain access to current research projects alongside their studies.

Video

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GSCN virtual Banner 2020

The ICG is represented at the Annual German Stem Cell Network Conference

Happy to share that on September 23th 2020 from 15:30-15:45 Anja Trillhaase is going to present her work entitled “The influence of the 9p21 CAD risk locus on vascular calcification – an iPSC model” at the 8th Annual German Stem Cell Network (GSCN) Conference (Abstract T04 in session: Stem cells in disease modeling and drug development).

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Guest lecture by Valerie Allamand about Collagen VI-deficiency and its consequences on the myomatrix

On November 27, 2019 at 3 pm in the seminar room EG (MFC1) the guest lecture given by Valerie Allamand will take place.

You are happily invited! 

Valerie Allamand, PhD

Lund University & Research Center of Myology Inserm Paris, France

“Collagen VI-deficiency and its consequences on the myomatrix”

November 27, 2019, 3 p.m., Seminar Room EC (MFC1)

Valerie Allamand is a group leader at UMR S974-Institut de Myologie, Paris (France). Currently, she is working at Lund University as a visiting research fellow. Valerie Allamand studies the physiopathology and therapeutic approaches for ColVI-related myopathies.

Collagen VI-related myopathy is a group of disorders that affect skeletal muscles and connective tissue. Most affected individuals have muscle weakness and joint deformities called contractures that restrict movement of the affected joints and worsen over time. Researchers have described several forms of collagen VI-related myopathy, which range in severity: Bethlem myopathy is the mildest, an intermediate form is moderate in severity, and Ullrich congenital muscular dystrophy is the most severe. Currently, no cure is available.

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