Paolo Piazza– Head of Genomics Facility
Paolo Piazza studied at Universita' degli Studi di Milano, where he completed a degree in Biology and a PhD in Genetics. He joined the Department of Plant Sciences, University of Oxford, in 2003 to work on molecular aspects of evolution of plant shapes. Subsequently, he joined the High Throughput Genomics lab in 2009 within the Wellcome Trust Centre for Human Genetics in Oxford, where he became the section leader for the library preparation team and managed process improvement initiatives for the core. He joined the Imperial BRC Genomics Facility in 2016 as the Head of the Facility.
Anna Zekavati – Genomics Project Manager
Anna Zekavati obtained her MSc in Genetics Manipulation from the University of Sussex and her PhD in Molecular Immunology from the University of Kings College London. She completed a Postdoctoral position at the Institute of Child Health, UCL (University College London), investigating the genetic causes of hypertrophic cardiomyopathy using next generation sequencing. She joined University of Imperial College London in 2012 to set up the Imperial AHSC Clinical Genome Laboratory. That lab subsequently merged with the Imperial BRC Informatics Facility in order to form the existing Imperial BRC Genomics Facility. She has been leading the genomics lab and is currently the genomics project manager of the facility who leads the activities including advising clinical and scientific colleagues in and outside of Imperial College on experimental design of their projects, sample library preparation, sequencing and data delivery, and ensuring that projects are completed on time and within budget.
Leena Bhaw – Genomics Lab Technician
Leena Bhaw joined the Imperial BRC Genomics Facility as a research technician in January 2017. She has a Master Degree in Biomedical Science from London Metropolitan University and almost 8 years’ experience working in genomics facilities around London. She comes with various skills and knowledge in Next-generation sequencing, microarray, Sanger Sequencing and Single cell genomics from previous work in The Francis Crick Institute, National Institute for Medical Research, Queen Mary University and LGC Ltd. Her area of interests is mainly focused on the fast developing technologies in genomics to support scientists in their research studies.
Nathalie Lambie – Genomics Lab Technician
Nathalie Lambie joined Imperial BRC Genomics Facility, following 8 years of working experience at the MRC Genomics Core Lab where she gained expertise in Next-Generation Sequencing using Illumina MiSeq and HiSeq, microarrays and conventional Sanger sequencing and Genotyping. Prior to this, Nathalie worked at GSK in the RNA Profiling Department focusing primarily on the use of Affymetrix whole genome microarrays and TaqMan real-time quantitative PCR to support pre-clinical and clinical development. Nathalie graduated from the University of Royal Holloway in 2003 with a MSc in Biological Science Research studying the use of PCR to develop microsatellite markers to determine stock structure of southern blue whiting around South America.
Bahar Monibi – Genomics Lab Visiting Researcher
Bahar Monibi obtained her BSc in Biochemistry from University of Kings College London and her MSc in Molecular Medicine from the UCL (University College London). She has several years of management and consultancy experience in Acumen Pharmaceutical Recruitment and other industrial facilities in London. Bahar Monibi joined Imperial BRC Genomics Facility in 2017 as a visiting researcher.
Dalia Kasperaviciute – Bioinformatician and Geneticist
Dalia Kasperaviciute gained her PhD in Human Genetics at Vilnius University, where she studied human population genetic diversity and migrations. At the same time, she worked as a medical geneticist, carrying out molecular genetic diagnostic testing in the clinical laboratory of Vilnius University Hospital. Having completed her PhD, she investigated the genetics of neurological diseases and normal cognition at University College London, as well as gaining a Masters in Bioinformatics from Birkbeck, University of London. Now at the Imperial BRC Genomics Facility, she provides bioinformatics support for high-throughput sequencing-based clinical genomics projects.
Keerthi Sindhura Sannareddy – Bioinformatician
Keerthi Sannareddy received her Master's degree in Bioinformatics from University of Michigan, Ann Arbor. After graduating, she worked as a Research Associate for the Bioinformatics core facility at the University of Michigan working on multiple projects involving high throughput data analysis and interpretation. Later, she worked in an evolutionary genomics lab under Molly Przeworski at the University of Chicago on the analysis of whole genome sequencing data sets from flies and birds. She worked for a short term with Cancer Research UK, University of Cambridge as a Bioinformatician before joining the Imperial BRC Genomics Facility in November 2015.
Vacant - Bioinformatics Programmer
Jorge Ferrer – Scientific Lead
Jorge Ferrer is Chair in Genetics and Medicine, Head of the Section of Epigenomics and Disease, and Theme Leader for Genetics and Genomics in the NIHR Imperial Biomedical Research Centre. He is also a Wellcome Trust Senior Investigator. He received his medical degree and trained in Endocrinology at the University of Barcelona School of Medicine. He subsequently trained in genetics and transcriptional regulation in Washington University and Harvard University before returning to Barcelona in 1997. There he established a research team within Institut d’Investigacions Biomediques August Pi i Sunyer and CIBERDEM, a Spanish diabetes research network. He recently moved to Imperial College London where he has established a laboratory based at Imperial Centre for Translational and Experimental Medicine. Professor Ferrer is interested in understanding genome regulation of pancreatic beta cells and its implications for human diabetes. His team has combined genetic model systems and advanced genomics to address key questions in human beta cell biology, regeneration, and disease.