Recall that when the HGP was completed, more than 40 percent of the genes identified had unknown functions. The PANTHER database provides access to comprehensive and current functional assignments for human genes (and genes from other species).
Go to http://www.pantherdb.org/data/. In the frame on the left side of the screen locate the 'Quick links' and use the 'Whole genome function views' link to a view of a pie chart of current functional classes for human genes. Mouse over the pie chart to answer these questions. What percentage of human genes encode transcription factors? Cytoskeletal proteins? Transmembrane receptor regulatory/adaptor proteins?
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
The purpose of a sequence assembly is to what?
A
Use reads to build a conserved sequence
B
Use reads to build a consensus sequence
C
Use reads to form a vector
D
Use reads to form a labeled sequence

1
Understand the concept of sequence assembly: Sequence assembly is the process of aligning and merging fragments from a longer DNA sequence in order to reconstruct the original sequence.
Recognize the term 'reads': In genetics, 'reads' refer to the short sequences of DNA that are obtained from sequencing technologies.
Identify the goal of sequence assembly: The primary goal is to use these reads to build a consensus sequence, which represents the most likely sequence of the original DNA based on the overlapping reads.
Distinguish between 'consensus sequence' and other terms: A consensus sequence is a sequence derived from the alignment of multiple reads, reflecting the most common nucleotide at each position.
Clarify why other options are incorrect: Forming a vector or a labeled sequence are not the primary objectives of sequence assembly; these tasks are related to other processes in genetic engineering and analysis.
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Sequencing the Genome practice set
