In our research we use a wide spectrum of methods including genomics, radiomics, radiogenomics and biostatistical analysis.
Genomic analysis is the identification, measurement or comparison of genomic features such as DNA sequence, structural variation, gene expression, or regulatory and functional element annotation at a genomic scale. Methods for genomic analysis typically require high-throughput sequencing or microarray hybridization and bioinformatics.
In our work we use next methods:
In the field of medicine, radiomics is a method that extracts large amount of features from radiographic medical images using data-characterisation algorithms. The hypothesis of radiomics is that the distinctive imaging features between disease forms may be useful for predicting prognosis and therapeutic response for various conditions, thus providing valuable information for personalized therapy.
We perform in-depth analysis of CT, MRI and USG image data such as:
Since the turn of the twentieth century, radiological images have been used to diagnose disease on a large scale, and has been used successfully to diagnose conditions affecting every organ and tissue type in the body. This is because tissue imaging correlates with tissue pathology. The addition of genomic data in the last twenty years, including DNA microarrays, miRNA, RNA-Seq allows new correlations to be made between cellular genomics and tissue-scale imaging.