Insertions are mutations in which extra base pairs are inserted into a new place in the DNA.
Deletions are mutations in which a section of DNA is lost, or deleted.
A karyotype is a preparation of the complete set of chromosomes in the cells of an individual organism, sorted by length, centromere location and other features.
Karyotyping is the process by which a karyotype is prepared from photographs of chromosomes, in order to determine the number of chromosomes and any abnormalities.
DNA, or deoxyribonucleic acid, is a universal molecule in all life on Earth.
It serves as the code dictating the shape and structure of living organism
This breakthrough enabled a profound understanding of reproduction and inheritance.
James Watson and Francis Crick's DNA model revealed the "secret of life."
The known DNA structure clarified its ability to divide, replicate, and pass on information.
DNA is a macromolecule composed of repeating nucleotide units.
Nucleotides consist of a phosphate, deoxyribose sugar, and a base.
Adenine, cytosine, thymine, and guanine are the four bases forming a genetic code.
The sequence of bases in DNA determines the organism's characteristics.
The structure of DNA is a double helix formed by two chains of nucleotides.
These chains are held together by the bonding of bases, creating the genetic code.
The structure composed of one nucleic acid, one phosphate, and one deoxyribose is called a nucleotide.
Cytosine pairs with guanine among the nucleic acids
Guanine pairs with cytosine.
Thymine pairs with adenine.
Adenine pairs with thymine
The arrangement of the two complementary DNA strands is referred to as "anti-parallel."
The phosphate and deoxyribose sugar are the two parts of a nucleotide that form the "backbone" of the DNA molecule
Dihybrid crosses involve the simultaneous inheritance of two different traits.
Each trait is controlled by a separate gene located on different chromosomes.
The principle of independent assortment states that alleles for different traits segregate independently during gamete formation.
Punnett squares are commonly used to predict the outcomes of dihybrid crosses.
The multiplication rule is applied to calculate the probability of inheriting specific combinations of alleles for two traits.
Dihybrid crosses contribute to understanding the genetic diversity and assortment of traits in offspring.
The phenotypic ratio resulting from a dihybrid cross is 9:3:3:1, following Mendel's law of segregation and independent assortment.
Dihybrid crosses provide insights into the genetic basis of complex traits controlled by multiple genes.
Genetics is the study of genes, heredity, and the variation of inherited traits in living organisms.
Genes are segments of DNA that encode instructions for the synthesis of proteins and influence an organism's characteristics.
Inheritance patterns follow Mendel's laws, including the law of segregation and the law of independent assortment.
The genome is the entire set of genetic material present in an organism.
Genotypes represent the genetic makeup of an individual, while phenotypes are the observable traits influenced by genes.
Alleles are alternative forms of a gene, and their combinations determine variations in traits.
Genetic mutations can lead to variations and contribute to evolution over time.
Genetic disorders result from abnormal variations or mutations in the DNA sequence.
Population genetics examines the distribution of genetic variations within and among populations.
Genetic diversity is crucial for the adaptation and survival of species in changing environments.