chapter 20: genomics and proteomic Flashcards
define genomics
Field of genetics that attempts to uderstand the content, organization function and evolution of the genetic information in whole genomes
genetic maps
- approximation of the location of genes relative to other genes
- based on recombination
-use cM or map units
what are come characteristics of genetic maps
- low resolution
-not always accurate - based on rates of crossing over
physical maps
based on the direct analysis of dna and they place genes in relation to distances
- measured in number of base pairs, kilobases, or mega base
high recombination=
father genes
- List some problems associated with sequencing of an entire genome
- whole genome sequencing
- only small fragments can be sequenced at a time
- must fragment genome into millions of small overlapping fragments
- how to order them after fragments are sequenced
goals of human genome project
- developing sequencing technology
- sequence genomes of model organims
- determine sequence of the human genome
- identify all genes in human genome
what were the two projects of the human genome project
- internatinoal human genome sequencing (public effor)
- celera genomics (private effort)
- Give the percent similarity between two humans
99.99%
- Define single nucleotide polymorphisms and haplotype (fig 20.8)
SNP: mutation where a single base pair in a DNA sequence differs
haplotype: A haplotype is a group of alleles in an organism that are inherited together from a single parent. Haplotypes are groups of SNPs that are inherited as a single block.
- Explain how SNPs can be used for genome wide association studies
- can help tell you the overall risk of developing a disease
how many base pairs in the human genome
3.2 billion
how many base pairs difference between you and your neighbor
4000cM
○ What is a contig
§ Set of two or more overlapping dna fragments that form a continuous stretch of dna
what is bioinformatics
molecular biology + computer science
- identify genes
-annotate genes