Step 1: The Human Genome refers to the complete set of genetic material in human cells, including all the DNA sequences. The human genome consists of about 3 billion base pairs of DNA.
Step 2: Key features of the human genome include:
1. Number of Genes: The human genome contains approximately 20,000-25,000 protein-coding genes.
2. Chromosomes: The genome is divided into 23 pairs of chromosomes, including 22 autosomal pairs and one pair of sex chromosomes (XX or XY).
3. Non-Coding DNA: A significant portion of the human genome does not code for proteins but plays important regulatory roles, including non-coding RNAs and introns.
4. Genetic Variation: There is significant genetic diversity within the human population, leading to differences in traits and susceptibility to diseases. 5. Mapping and Sequencing: The Human Genome Project, completed in 2003, successfully mapped the entire human genome, providing crucial information for medical research and disease prevention.
Step 3: Understanding the human genome has paved the way for advancements in personalized medicine, gene therapy, and understanding genetic diseases.
In a practical examination, the following pedigree chart was given as a spotter for identification. The students identify the given pedigree chart as
Identify which one of the given pair of options is correct with respect to Down's syndrome and Turner's syndrome
(b) Order of the differential equation: $ 5x^3 \frac{d^3y}{dx^3} - 3\left(\frac{dy}{dx}\right)^2 + \left(\frac{d^2y}{dx^2}\right)^4 + y = 0 $