Table of contents

1. Introduction to Genetics51m
2. Mendel's Laws of Inheritance3h 37m
3. Extensions to Mendelian Inheritance2h 41m
4. Genetic Mapping and Linkage2h 28m
5. Genetics of Bacteria and Viruses1h 21m
6. Chromosomal Variation1h 48m
7. DNA and Chromosome Structure56m
8. DNA Replication1h 10m
9. Mitosis and Meiosis1h 34m
10. Transcription1h 0m
11. Translation58m
12. Gene Regulation in Prokaryotes1h 19m
13. Gene Regulation in Eukaryotes44m
14. Genetic Control of Development44m
15. Genomes and Genomics1h 50m
16. Transposable Elements47m
17. Mutation, Repair, and Recombination1h 6m
18. Molecular Genetic Tools19m
- Genetic Cloning
  9m
- Methods for Analyzing DNA
  9m
19. Cancer Genetics29m
- Overview of Cancer
  21m
- Cancer Mutations
  7m
20. Quantitative Genetics1h 26m
21. Population Genetics50m
- Hardy Weinberg
  19m
- Allelic Frequency Changes
  31m
22. Evolutionary Genetics29m

15. Genomes and Genomics

Overview of Genomics

Genetics

15. Genomes and Genomics

Overview of Genomics

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Multiple Choice

Which of the following technologies is most useful for high-throughput sequencing in genomics?

Sanger sequencing

Gel electrophoresis

Illumina sequencing

Polymerase chain reaction (PCR)

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Verified step by step guidance

Understand the goal: High-throughput sequencing refers to technologies that can sequence millions of DNA fragments simultaneously, allowing rapid and large-scale genomic analysis.

Review each option's purpose: Sanger sequencing is a traditional method that sequences DNA fragments one at a time, making it low-throughput.

Gel electrophoresis is a technique used to separate DNA fragments by size but does not sequence DNA itself.

Polymerase chain reaction (PCR) is used to amplify specific DNA regions but does not perform sequencing.

Illumina sequencing is a next-generation sequencing technology designed for high-throughput sequencing, capable of processing millions of DNA fragments in parallel, making it the most suitable choice for large-scale genomic studies.