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
2:03 minutes
Problem 3c
Textbook Question
Textbook QuestionWhen the whole-genome shotgun sequence of the Drosophila genome was assembled, it comprised 134 scaffolds made up of 1636 contigs. Why were there so many more contigs than scaffolds?
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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Contigs and Scaffolds
Contigs are contiguous sequences of DNA that are assembled from overlapping DNA fragments, representing a continuous stretch of the genome. Scaffolds, on the other hand, are larger structures that consist of multiple contigs linked together, often with gaps. The presence of more contigs than scaffolds indicates that many short sequences were assembled, but not all could be connected into longer, continuous scaffolds due to gaps or unresolved regions.
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Genome Assembly
Genome assembly is the process of reconstructing the complete sequence of a genome from short DNA fragments obtained through sequencing. This process involves aligning and merging overlapping sequences to form longer contiguous sequences (contigs) and then organizing these contigs into scaffolds. The complexity of the genome, including repetitive regions and structural variations, can lead to a higher number of contigs compared to scaffolds.
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Genomics Overview
Repetitive DNA and Gaps
Repetitive DNA sequences can complicate genome assembly because they can lead to ambiguities in determining the correct order of fragments. These regions may cause difficulties in linking contigs into scaffolds, resulting in gaps where the sequence is unresolved. The presence of many contigs relative to scaffolds often reflects the challenges posed by these repetitive elements and the limitations of the sequencing technology used.
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