The Co-Evolution of Genetics and Statistics Bio-Stat seminar 2 February 2011.

Slides:



Advertisements
Similar presentations
Lecture 41 Prof Duncan Shaw. Genetic Variation Already know that genes have different alleles - how do these arise? Process of mutation - an alteration/change.
Advertisements

Genetic Inheritance & Variation
Lecture 2 Strachan and Read Chapter 13
Single Nucleotide Polymorphism And Association Studies Stat 115 Dec 12, 2006.
Note that the genetic map is different for men and women Recombination frequency is higher in meiosis in women.
Tutorial #1 by Ma’ayan Fishelson
Introduction to genomes & genome browsers
Gene Linkage and Genetic Mapping
Genetics.
Genetica per Scienze Naturali a.a prof S. Presciuttini Human and chimpanzee genomes The human and chimpanzee genomes—with their 5-million-year history.
pt 10 pt 15 pt 15 pt 20 pt 20 pt 25 pt 25 pt 5 pt 5 pt 10 pt 10 pt 15 pt 15 pt 20 pt 20 pt 25 pt 25 pt 5 pt 5 pt 10 pt 10 pt 15 pt 15 pt 20 pt.
Introduction to Linkage Analysis March Stages of Genetic Mapping Are there genes influencing this trait? Epidemiological studies Where are those.
Nucleic Acids 101. Last week’s grand challenge: Reading and interpreting genetic information.
Objectives Students will be able to describe the patterns of inheritance that Mendel’s data revealed. Students will be able to summarize Mendel’s Law of.
Chromosomes carry genetic information
Restriction Fragment Length Polymorphisms (RFLPs) By Amr S. Moustafa, M.D.; Ph.D. Assistant Prof. & Consultant, Medical Biochemistry Dept. College of.
Chromosomes, Mapping, and the Meiosis-Inheritance Connection
Mendel and Heredity Section 1: The Origins of Genetics
Analyzing DNA Differences PHAR 308 March 2009 Dr. Tim Bloom.
Single Nucleotide Polymorphisms Mrs. Stewart Medical Interventions Central Magnet School.
1 Father of genetics. Studied traits in pea plants.
A little about how DNA works David Sloane, MD Special Studies, HGSE Brigham and Women’s Hospital Harvard Medical School 2/10/2014David.
National Taiwan University Department of Computer Science and Information Engineering Haplotype Inference Yao-Ting Huang Kun-Mao Chao.
The Complexities of Data Analysis in Human Genetics Marylyn DeRiggi Ritchie, Ph.D. Center for Human Genetics Research Vanderbilt University Nashville,
Non-Mendelian Genetics
Allele. Alternate form of a gene gene variant autosome.
Chapter 3 Genetics: The Science of Heredity Section 1: Mendel’s Work.
Chromosomes, Mapping, and the Meiosis-Inheritance Connection Chapter 13.
Genetics and Inheritance Year 10 Biology Part 1: Genes & Chromosomes.
CS177 Lecture 10 SNPs and Human Genetic Variation
GWAS Hits and Functional Implications Peter Castaldi February 1, 2013.
Genome-Wide Association Study (GWAS)
Continuity Through Heredity. The Dual Role of Genetic Material  Heredity – the transmission of genetic information from one generation to another  The.
National Taiwan University Department of Computer Science and Information Engineering Pattern Identification in a Haplotype Block * Kun-Mao Chao Department.
Linkage and Mapping. Figure 4-8 For linked genes, recombinant frequencies are less than 50 percent.
ABC for the AEA Basic biological concepts for genetic epidemiology Martin Kennedy Department of Pathology Christchurch School of Medicine.
Single Gene Inheritance
February 20, 2002 UD, Newark, DE SNPs, Haplotypes, Alleles.
In The Name of GOD Genetic Polymorphism M.Dianatpour MLD,PHD.
The Future of Genetics Research Lesson 7. Human Genome Project 13 year project to sequence human genome and other species (fruit fly, mice yeast, nematodes,
Slide 1 of 43 Biology Mr. Karns Human Heredity. Slide 2 of 43 14–1 Human Heredity 14-1 Human Heredity.
Chapter 23: Evaluation of the Strength of Forensic DNA Profiling Results.
Genetics Intro. Phenotype Observable, Physical traits (ear shape, petal color) these are expressed biologically. –Offspring usually have a phenotype similar.
From: Scheinfeld A (1965) Your heredity and environment. JB Lippincott Company, Philadelphia Phenotypic variation among humans is enormous.
The Haplotype Blocks Problems Wu Ling-Yun
1 Finding disease genes: A challenge for Medicine, Mathematics and Computer Science Andrew Collins, Professor of Genetic Epidemiology and Bioinformatics.
GENOME ORGANIZATION AS REVEALED BY GENOME MAPPING WHY MAP GENOMES? HOW TO MAP GENOMES?
6.3 Mendel and Heredity KEY CONCEPT Mendel’s research showed that traits are inherited as discrete units.
6.3 Mendel and Heredity.
Chapter 4, Heredity and Evolution
Chromosomal Basis of Inheritance Lecture 13 Fall 2008
Heredity Chapter 11 Green Book.
Chapter 6, sections Mendelian Genetics.
School of Pharmacy, University of Nizwa
Gene Hunting: Design and statistics
Gene Mutations.
Mutations.
Heredity Lesson 8.
February 7, 2016 Journal: Why do you and your siblings have different traits even though you have the same parents?
Mutations changes in the DNA sequence that can be inherited
Mutations & Genetic Engineering
1.
Unit 6 “Genetics” 18 Words.
School of Pharmacy, University of Nizwa
Genetics: Inheritance
Genetic Disorders.
Mendel laid the groundwork for genetics.
Genetic terms.
Jeopardy Final Jeopardy DNA People Protein Synthesis Mutations Random
Friday, oct 13th Get your binder You need:
Presentation transcript:

The Co-Evolution of Genetics and Statistics Bio-Stat seminar 2 February 2011

From the First Gregor Mendel is recognized as the founder of genetics Was the first to use “math” to define a biologic process.

Role of Biostat Fisher suggested in 1936 that Mendel’s data was a little too good. Fisher is thought of as a geneticist.

The Chemistry of DNA

Structure of DNA Double helix=2nm 10 Base pairs/turn=10nm 140 BP/nucleosome

How Has “Math” Driven Genetics? Genotype GG=0.25 Gg=0.50 gg=0.25 Phenotype Gx=0.75 gg=0.25

Some Questions in Genetics There are 4 bases in DNA There are 20 amino acids How do you order 4 to code for 20?

Simple Math 4=4 4X4=16 4X4X4=64 So 3 bases required at a minimum

More Questions If 3 required, spacing? Boxcar= ATGCAGT Sequential=ATGCAGT Spaced=ATGaCAGaT Solution First a homo-polymer (TTTTTTT) This produce a peptide of phenylalanine Then a co-polymer TTCCTTCCTTCC The pattern of AA would allow dissection

Example TTCCTTCCTTCCTTCCTTCC Boxcar Sequential TTC=Phe TTC=Phe TCC=Ser CTT=Leu CCT=Pro CCT=Pro CTT=Leu TCC=Ser

How Did We Get Here? Genetics is the study of variation “Easy” genetics involved variation by genes of major effect. Sickle cell, cystic fibrosis are examples of single gene diseases

Finding Single Genes Collect families that show the trait Analyze their DNA find sections that are common with trait Assess the probability that these are shared randomly LOd ratio

How is DNA Measured? Before the age of the genome, centimorgans Humans have 22 paired chromosomes These segregate at cell division independently Along a chromosome the probability that a trait is near something is measured in centimorgans

DNA is in Base Pairs Now The chromosomes are numbered largest to smallest (1-22) Positions are now located by Chr # and position along that Chr. (Chr2: ) There are a little more than 3x10 9 BP

Mutations vs. SNP Currently the trend is to talk of “variation” not mutation. SNP=Single Nucleotide Polymorphism Most SNP are dimeric (A/G) and have a frequency (0.895/0.105) SNP’s mark positions not “mutations”!

Other Terms InDel VNTR marker Coding Non- Coding synonymous promoter epigenetic imprinting mitochondria l Intron/exon

Data Sets Arrays SNP Expressio n Genotype SNP - Looking for regions of DNA associated with a trait Phenotype Expression - What genes are “produced” How the biochemistry is changed

Help From the “Math”Gifted! These are complex datasets Analysis can be “simple”, it shouldn’t be! Getting in early is critical

Next Big Challenge Network analysis Andrew Mugler, Boris Grinshpun, Riley Franks, and Chris H. WigginsStatistical method for revealing form-function relations in biological networksPNAS (2) ; published ahead of print December 23, 2010, doi: /pnas.