Greek Genome Center
Services
DNA-seq
DNA sequencing is the process of determining the precise order of nucleotides within a DNA molecule. The advent of rapid DNA sequencing methods has greatly accelerated biological and medical research and discovery. Among others, DNA sequencing is used for identifying:
The complete DNA sequence of an organism’s genome (Whole Genome Seq, WGS)
The precise DNA sequencing of all the protein-coding genes in a genome (Whole Exome Seq, WES) or of a specific group of genes (Gene Panel Seq)
The binding sites of a DNA-associated protein (ChIP-seq)
The DNA regions in the genome associated with regulatory activity (DNAse-seq, FAIRE-seq)
The sequences that act as transcriptional enhancers (STARR-seq)
RNA-seq
A high resolution tool for studying changes in the coding and noncoding regions of the transcriptome. RNA-Seq enables the sensitive and accurate measurement of differential gene expression over time or in different groups, conditions and treatments. RNA-Seq also enables the detection of transcript isoforms, gene fusions, single nucleotide variants (SNVs) and allele-specific gene expression.
Team

Dimitris Thanos
Director

Periklis Makrythanasis
Supervising Scientist

Katerina Zoi
Molecular Geneticist

Emmanouil Athanasiadis
Computational Biologist

Ioannis Vatsellas
Wet Lab Scientific Manager

Giorgos Panagopoulos
Laboratory Scientist

Artemis Korovesi
Laboratory Scientist

Theodoros Loupis
Laboratory Scientist, Bioinformatician