Implementation and clinical utility of the GATK gCNV pipeline for rare disease diagnostics using whole exome sequencing

Djordje Pavlovic1*, Anita Skakic1, Kristel Klaassen1, Irena Marjanovic1, Marina Parezanovic1, Nina Stevanovic1, Goran Cuturilo2, Marija Brankovic2, Brankica Bosankic2, Jelena Ruml Stojanovic2, Bojan Ristivojevic1, Branka Zukic1, Maja Stojiljkovic1 and Marina Andjelkovic1

1Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Serbia

2University Children's Hospital, Belgrade, Serbia

Precision and recall in rare disease genomics: benchmarking the IMGGE whole genome sequencing pipeline

Sara Stankovic1*, Nikola Jocic1, Djordje Pavlovic1, Marina Parezanovic1, Nina Stevanovic1, Kristina Grujic1, Jovana Komazec1, Kristel Klaassen1, Anita Skakic1, Marina Andjelkovic1, Milena Ugrin1, Vesna Spasovski1, Steven Laurie2 and Maja Stojiljkovic1

1Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Serbia

2Centro Nacional de Análisis Genómico, Barcelona, Spain

Integrated transcriptomic analysis reveals coordinated network reprogramming and p53 pathway inactivation in temozolomide-resistant gioblastoma A172 cell line

Milica Pajović*, Ana Podolski-Renić, Jelena Dinić, Marija Grozdanić, Milica Pešić, Sofija Bjeletić, Sofija Jovanović Stojanov, Ema Lupšić and Miodrag Dragoj

Institute for Biological Research "Siniša Stanković" – National Institute of Republic of Serbia, University of Belgrade