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.
What are the strengths and weaknesses of this approach?
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
What is the name of a short sequenced DNA fragment?
A
Read
B
Contig
C
Consensus Sequence
D
Overlaps

1
Understand the context: In genetics, sequencing involves determining the order of nucleotides in a DNA fragment.
Identify the term 'Read': A 'Read' is a short sequence of DNA obtained from sequencing technology, representing a fragment of the original DNA.
Differentiate between terms: A 'Contig' is a set of overlapping DNA segments that together represent a consensus region of DNA, while a 'Consensus Sequence' is a sequence derived from aligning multiple reads to find the most likely sequence.
Recognize 'Overlaps': These are regions where different reads share common sequences, helping in assembling contigs.
Conclude: The term 'Read' specifically refers to the short sequenced DNA fragment obtained directly from sequencing.
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