Statistics for Human Genetics and Molecular Biology Lecture 1: Review Basic Terminology of Genetics

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1/25 Statistics for Human Genetics and Molecular Biology Lecture 1: Review Basic Terminology of Genetics Dr. Yen-Yi Ho (yho@umn.edu) Sep 09, 2015

2/25 Logistics Lectures M W F & Labs: 1:25 to 2:15 Office Hours : Yen-Yi MW 2:30-3:30 Cavan MW 2:30-3:30 Zhiyuan (Jason) Xu Tue 3-4p in Mayo A446 Textbook: Foulkes (2009): Applied Statistical Genetics with R Hahne, Huber, Gentleman, and Falcon (2008): Bioconductor Case Studies John Verzani s SimpleR notes Website: http://www.biostat.umn.edu/ cavanr/pubh7445.html

3/25 Goals for the Course Basic knowledge of R Basics of statistics for human genetics Basics of genetic data analyses using R/Bioconductor Interpreting results and simple diagnoses

4/25 Objectives of Lecture 1 Review basic terminology of genetics Central dogma of molecular biology Chromosomes, genes, DNA, RNA, and proteins Gene expression Genetic variation Mutations Technologies for Genome Analysis

/25 Mendelian Genetics (1866) Segregation of alleles in the production of sex cells 1. the principle of segregation 2. the principle of independent assortment

6/25 Mendelian Genetics Translates to Modern Genetics A parent contributes only a single chromosome within a pair to the offspring. A fixed location on a chromosome pair is called a locus, and only those loci coding (for proteins or functional RNA) are typically called genes. An allele is the state or type of genetic info at a locus on a single chromosome. Thus there are two alleles at each locus in an individual (for autosomes, and for sex chromosomes in females).

7/25 Example: A particular disease locus has two possible allele types in the population: d (the disease allele) and D (normal). Genotype: the joint (unordered) state of the two alleles. Could be dd, DD (called homozygous genotypes), or Dd ( heterozygous genotype). Alleles that are common in the population are often called wild type while disease alleles are called mutant. Phenotype: an observed trait we care about, such as disease status, etc.

Mendelian Genetics Translates to Modern Genetics 8/25 Adapted from NHGRI Talking Glossary

9/25 Central Dogma of Biology: Classic View

10/25

1/25 Base Pairs IUPAC code Base a adenine c cytosine g guanine t (or u) thymine (or uracil) r a/g y c/t s g/c w a/t k g/t m a/c b c/g/t d a/g/t h a/c/t v a/c/g n any base./ - gap Humans have 3 10 9 base pairs in their nuclear genome.

Gene Gene: a functional and inheritable element in the genome, usually codes for a protein; human genome 20,000 genes. The gene consists of three major structures: Regulatory segment Exons Introns 12/25 souce: http://www.nobelprize.org/educational/medicine/dna/a/replication/gene.html

13/25 Transcription Transcription is the process of making RNA from DNA.

14/25 Translation Translation is the process of translating the sequence of nucleotide bases in DNA/RNA into a sequence of amino acids in a protein.

5/25

6/25 Gene Expression Gene expression is a highly specific process. Only a small fraction of the genes are expressed, or turned on, in any particular type of cell. gene expression in different tissues gene expression in the same tissue, but different points in time

7/25 Putting it all together DNA: Info on chromosome is static, and essentially the same across cells within the individual mrna: Not as relevant as protein, but easier to quantify Protein: Difficult to quantify globally, though very relevant source: http://www.nobelprize.org/educational/medicine/dna/index.html

Source of Variation 18/25

19/25 Environment Vs. Gene Any two individuals are 99.9% identical in their DNA

0/25 Genetic Variations (Polymorphisms) That 0.1 % is very important in defining our differences single nucleotide polymorphisms (SNPs, every 300 nucleotide on average) small-scale mutation, insertions, deletions copy number variations (AAGAAGAAGAAG) source: http://ghr.nlm.nih.gov/handbook/genomicresearch/snp

Mutations 21/25

2/25 Genome Analysis Technologies 1. DNA Microarrays: SNP, Copy number variation (CNV), Methylation DNA sequencing: SNP, Insertion, Deletion, Mutation, CNV, Methylation 2. mrna Microarrays RNA sequencing 3. Protein 2-D electrophoresis Maldi-Tof mass spec

General Steps in Obtaining Gene Expression Data 23/25

General Steps in Next-Generation Sequencing 24/25

25/25 Next Lecture Review basic terminology of population genetics Crossing Over DNA Recombination Genetic Markers Genetic Association Analysis Structures of Genetic Data