Tag Archives: IMGGE

IMGGE is an Associated Partner in RD-Connect

December 2014.

IMGGE has been appointed the Associated Partner in RD-Connect.

RD-Connect is a unique global infrastructure project that links up databases, registries, biobanks and clinical bioinformatics data used in rare disease research into a central resource for researchers worldwide.

In March 2015, RD-Connect and NeurOmics held their annual meetings in Palma de Mallorca at the beginning of March 2015. Both meetings proved to be a great opportunity for project partners, associated partners and committee members to report on progress and achievements over the past year and to plan for future work. IMGGE participated as an associated partner.

Evropska Noć Istraživača u IMGGI

NI-2011Povodom obeležavanja Evropske Noći Istraživača u organizaciji SERBORDISinn projekta, pozivamo vas da posetite Institut za molekularnu genetiku i genetičko inženjerstvo Univerziteta u Beogradu (IMGGI) i saznate nešto više o genima i retkim bolestima. Imaćete priliku da sami izolujete svoju DNK kroz eksperiment koji je osmišljen tako da koristite namirnice koje su u svakodnevnoj upotrebi (tečni sapun, kuhinjska so, sok od ananasa itd).

Svaki čovek nosi jedinstven i neponovljiv DNK zapis u svojim genima. Zahvaljujući napretku nauke i istraživanjima širom sveta i kod nas, u današnje vreme raspolažemo metodama kojima možemo da pročitamo DNK zapis svakog čoveka. Primena ovih metoda je posebno važna u slučaju retkih bolesti jer omogućava postavljanje dijagnoze.

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Očekujemo vas u PETAK, 26. SEPTEMBRA 2014. od 12 do 15 časova na adresi Vojvode Stepe 444a, 11010 Beograd.

SERBORDISinn projekat, www.serbordisinn.rs, www.imgge.bg.ac.rs

Upcoming Symposium: Genomics of Rare Diseases

October 30th – November 1st, 2014, Belgrade, Republic of Serbia

The Symposium Faculty consists of international renowned speakers from Europe, the US and Asia.

The meeting will highlight the implementation of genomics to elucidate the molecular etiology of rare diseases in Serbia and the surrounding countries, as part of the EC-funded SERBORDISinn project.

Lastly, the meeting will feature the 2014 Genomic Medicine Alliance – pUblic Health Genomics award, presented for the best abstract submitted for this meeting.

Registration will open in July 2014.

For more information, registration and abstract submission, please click here to visit Golden Helix web site.
Download SCIENTIFIC PROGRAM of Genomics of Rare Diseases of Genomics of Rare Diseases Symposium in PDF format.

Premier NGS in IMGGE

Sophisticated research equipment, the Next-generation sequencing System (MiSeq, Illumina) has come to IMGGE. It will enable implementation of cutting-edge methodology for the study of molecular markers of rare diseases in the IMGGE.

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The first run on MiSeq Illumina has been successfully completed in IMGGE. Samples of childhood and adult acute myeloid and acute lymphoid leukemia, as well as lymphoma samples have been analyzed using TruSeq Amplicon – Cancer Panel (TSACP).

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To be continued…