Biology, Genetics and Bioinformatics Unit

Revolutionary Breakthroughs in CRISPR Technology: Editing the Human Genome

In recent years, CRISPR technology has emerged as one of the most revolutionary tools in molecular biology, holding the potential to redefine the future of human genetics. As a precise, efficient, and relatively simple method of editing genes, CRISPR has become a powerful tool for scientists looking to correct genetic defects, treat diseases, and explore …

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New research in genetics. How genes influence a person’s character

Genetics is a branch of the science of biology that studies the development of organisms and heredity. It is an integrative biological discipline that studies two fundamental properties of all living things: variability and hereditary environment. The main sections of genetics are: – Molecular genetics – Human genetics – Genetics of microorganisms – Plant genetics …

What is the difference between biology and general biology?

Biology is the science of life that studies all living organisms, including their structure, function, behaviour and interaction with the environment. General biology is the branch of biology that studies the general patterns of life inherent in all living organisms. The main difference between biology and general biology is that biology covers all aspects of …

What does the science of genetics study in biology?

Genetics is the branch of biology that studies the heredity and variability of organisms. It investigates how traits are passed from parents to offspring and how these traits can change. Genetics includes the following main areas: Molecular genetics studies the structure and function of genes and the processes that regulate their activity. Cellular genetics studies …

Types of inheritance of genetically determined diseases

There are three main types of inheritance of genetically determined diseases: autosomal dominant, autosomal recessive and sex-linked. Autosomal dominant inheritance means that a single copy of a mutated gene is sufficient to develop a disease. If one parent has an autosomal dominant disease, each of their children has a 50% chance of inheriting the disease. …

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How to read the genome

Genome reading, or sequencing, is the process of determining the sequence of nucleotides (A, T, C, and G) in an organism’s DNA. Genome sequencing plays an important role in biological research and medical diagnosis. Here are the basic steps that the genome sequencing process usually involves: DNA extraction: The first step is to obtain a …

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