✅ Answer: B) 2001
🔬 Explanation: The Human Genome Project (HGP) was launched in 1990 and officially announced its first draft sequence in 2001. A more refined version followed in 2003, but 2022-2023 marked the release of a truly complete human genome (including centromeres and telomeres).
✅ Answer: A) Clone-by-Clone & Shotgun Sequencing
🔬 Explanation:
✅ Answer: B) Shotgun Sequencing
🔬 Explanation: Shotgun sequencing allowed scientists to rapidly sequence DNA but led to errors due to repeated sequences and gaps. Clone-by-Clone was slower but more accurate.
✅ Answer: C) $3 billion
🔬 Explanation: The project took 13 years (1990–2003) and cost $3 billion, but now, sequencing a human genome costs less than $1,000! 📉💰
✅ Answer: C) 45%
🔬 Explanation: Nearly half of the human genome is made up of repetitive sequences from ancient transposable elements. Scientists once called this "junk DNA," but we now know some of it regulates gene expression!
✅ Answer: C) Small genetic variations that make individuals unique
🔬 Explanation: SNPs are single-letter DNA changes that make people unique. They influence traits like eye color, height, and disease risk. 🌱
✅ Answer: C) Cystic fibrosis
🔬 Explanation:
✅ Answer: C) Polygenic traits
🔬 Explanation: Traits like height, diabetes risk, and intelligence are affected by many genes (polygenic) and environmental factors (nutrition, lifestyle, etc.).
✅ Answer: C) The tendency of certain genetic variants to be inherited together due to proximity on a chromosome
🔬 Explanation: LD happens because nearby genes don’t always get shuffled during reproduction. This helps scientists predict disease-linked genes without sequencing every variation.
✅ Answer: B) To find genetic variants associated with diseases
🔬 Explanation: GWAS scans thousands of genomes to find SNPs linked to diseases like diabetes, Alzheimer's, or cancer. This helps scientists identify genetic risk factors.
✅ Answer: C) 26,000
🔬 Explanation: Originally, scientists thought we had 100,000+ genes, but it turns out we only have about 26,000—fewer than some plants! 🌿 The complexity of humans comes from how genes are regulated, not the number of genes.
✅ Answer: B) Gregor Mendel
🔬 Explanation:
✅ Answer: B) A stretch of DNA that codes for a specific function
🔬 Explanation:
✅ Answer: B) CRISPR-Cas9
🔬 Explanation: CRISPR is a gene-editing tool inspired by bacteria’s immune system. It lets scientists cut and modify DNA precisely, opening doors to gene therapy, disease prevention, and biotechnology innovations.
✅ Answer: B) Precision medicine (custom treatments based on a person’s genome)
🔬 Explanation:
💯 15/15 – Genome Master! 🧬 You could be a geneticist!
🔬 12-14 – Impressive! You have a strong grasp of genomics.
📚 8-11 – Great effort! Keep learning, and you’ll master it.
🧐 5-7 – Not bad! A little more studying, and you’ll be a pro.
🤔 0-4 – Keep exploring! Genomics is a vast, exciting field.
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Genomics is an amazing field—you're on your way to mastering it! 🚀😊