Whole-exome sequencing (WES) is helping physicians diagnose a genetic condition that has defied diagnosis by traditional means. The implication here is that exons in the nuclear genome are sequenced in the hopes that, by comparison with the genomes of nonaffected individuals, a diagnosis might be revealed.
If you were ordering WES for a patient, would you also include an analysis of the patient's mitochondrial genome?
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
- 19. Cancer Genetics29m
- 20. Quantitative Genetics1h 26m
- 21. Population Genetics50m
- 22. Evolutionary Genetics29m
15. Genomes and Genomics
Sequencing the Genome
Struggling with Genetics?
Join thousands of students who trust us to help them ace their exams!Watch the first videoMultiple Choice
Restriction enzymes are proteins responsible for what?
A
Labeling DNA with molecular probes
B
Chopping the DNA at specific sequences
C
Amplifying a short DNA sequence
D
Compiling paired end reads

1
Understand that restriction enzymes are proteins that act as molecular scissors.
Recognize that these enzymes cut DNA at specific sequences, known as recognition sites.
Note that each restriction enzyme has a unique recognition sequence, usually 4-8 base pairs long.
Realize that the primary function of restriction enzymes is to cleave DNA at these specific sites, which is crucial for various genetic engineering techniques.
Remember that restriction enzymes do not label DNA, amplify DNA, or compile paired end reads; their main role is to chop DNA at specific sequences.
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