Single Nucleotide Polymorphisms (SNPs) By Amira Jhelum Rahul Shweta.

Slides:



Advertisements
Similar presentations
CZ5225 Methods in Computational Biology Lecture 9: Pharmacogenetics and individual variation of drug response CZ5225 Methods in Computational Biology.
Advertisements

Major insights from the HGP on Nature (2001) 15 th Feb Vol 409 special issue; pgs 814 & )Gene content 2)Proteome content 3)SNP identification.
Chapter 19 Evolutionary Genetics 18 and 20 April, 2004
Natural Selection on the Olfactory Receptor Gene Family in Humans and Chimpanzee Chloe Lee.
Phylogenetic Trees Understand the history and diversity of life. Systematics. –Study of biological diversity in evolutionary context. –Phylogeny is evolutionary.
Plant of the day! Pebble plants, Lithops, dwarf xerophytes Aizoaceae
Outline to SNP bioinformatics lecture
14 Molecular Evolution and Population Genetics
Predicting the Function of Single Nucleotide Polymorphisms Corey Harada Advisor: Eleazar Eskin.
Genetica per Scienze Naturali a.a prof S. Presciuttini Human and chimpanzee genomes The human and chimpanzee genomes—with their 5-million-year history.
Biology and Bioinformatics Gabor T. Marth Department of Biology, Boston College BI820 – Seminar in Quantitative and Computational Problems.
Analysis of Phenotypic Variations in the Mouse Genome Caused by Single Nucleotide Polymorphisms Corey Harada Advisor: Eleazar Eskin.
From population genetics to variation among species: Computing the rate of fixations.
SNP database 張學偉 助理教授 高雄醫學大學 生物醫學暨環境生物學系. SNP = Single Nucleotide Polymorphism (read in SNiP)
Introduction to Computational Biology Topics. Molecular Data Definition of data  DNA/RNA  Protein  Expression Basics of programming in Matlab  Vectors.
Polymorphism Structure of the Human Genome Gabor T. Marth Department of Biology Boston College Chestnut Hill, MA
SNP database 張學偉 助理教授 高雄醫學大學 生物醫學暨環境生物學系. SNP = Single Nucleotide Polymorphism (read in SNiP)
The origins & evolution of genome complexity Seth Donoughe Lynch & Conery (2003)
Molecular Evolution with an emphasis on substitution rates Gavin JD Smith State Key Laboratory of Emerging Infectious Diseases & Department of Microbiology.
Evolutionary Genome Biology Gabor T. Marth, D.Sc. Department of Biology, Boston College Medical Genomics Course – Debrecen, Hungary, May 2006.
PolyPhen and SIFT: Tools for predicting functional effects of SNPs Epi 244 Spring 2009 Sam S. Oh.
Adaptive Molecular Evolution Nonsynonymous vs Synonymous.
Polymorphisms – SNP, InDel, Transposon BMI/IBGP 730 Victor Jin, Ph.D. (Slides from Dr. Kun Huang) Department of Biomedical Informatics Ohio State University.
TGCAAACTCAAACTCTTTTGTTGTTCTTACTGTATCATTGCCCAGAATAT TCTGCCTGTCTTTAGAGGCTAATACATTGATTAGTGAATTCCAATGGGCA GAATCGTGATGCATTAAAGAGATGCTAATATTTTCACTGCTCCTCAATTT.
Computational Molecular Biology Biochem 218 – BioMedical Informatics Simple Nucleotide.
Modes of selection on quantitative traits. Directional selection The population responds to selection when the mean value changes in one direction Here,
Chapter 3 Substitution Patterns Presented by: Adrian Padilla.
1 Genetic Variability. 2 A population is monomorphic at a locus if there exists only one allele at the locus. A population is polymorphic at a locus if.
- any detectable change in DNA sequence eg. errors in DNA replication/repair - inherited ones of interest in evolutionary studies Deleterious - will be.
Haplotype Blocks An Overview A. Polanski Department of Statistics Rice University.
Cryptic Variation in the Human mutation rate Alan Hodgkinson Adam Eyre-Walker, Manolis Ladoukakis.
Doug Brutlag 2011 Genomics & Medicine Doug Brutlag Professor Emeritus of Biochemistry &
Models of Molecular Evolution I Level 3 Molecular Evolution and Bioinformatics Jim Provan Page and Holmes: Sections 7.1 – 7.2.
SNPs Daniel Fernandez Alejandro Quiroz Zárate. A SNP is defined as a single base change in a DNA sequence that occurs in a significant proportion (more.
©Edited by Mingrui Zhang, CS Department, Winona State University, 2008 Identifying Lung Cancer Risks.
Abstract To understand the population dynamics in rice we conducted detailed sequence study in 32 accessions of rice (10 japonica, 7 indica, 10 Asiatic.
SNP Haplotypes as Diagnostic Markers Shrish Tiwari CCMB, Hyderabad.
SNPs and the Human Genome Prof. Sorin Istrail. A SNP is a position in a genome at which two or more different bases occur in the population, each with.
Ch. 21 Genomes and their Evolution. New approaches have accelerated the pace of genome sequencing The human genome project began in 1990, using a three-stage.
Genetics Presentation: Sea Squirts Catherine Dong 9/6/12 Bio303 H Dr. Ely.
Korea BioInformation Center Byoung-Chul Kim
Chapter 24: Molecular and Genomic Evolution CHAPTER 24 Molecular and Genomic Evolution.
Models of Molecular Evolution III Level 3 Molecular Evolution and Bioinformatics Jim Provan Page and Holmes: Sections 7.5 – 7.8.
1 Population Genetics Basics. 2 Terminology review Allele Locus Diploid SNP.
What is a SNP?. Lecture topics What is a SNP? What use are they? SNP discovery SNP genotyping Introduction to Linkage Disequilibrium.
Julia N. Chapman, Alia Kamal, Archith Ramkumar, Owen L. Astrachan Duke University, Genome Revolution Focus, Department of Computer Science Sources
Chapter 5 The Content of the Genome 5.1 Introduction genome – The complete set of sequences in the genetic material of an organism. –It includes the.
Lecture 6. Functional Genomics: DNA microarrays and re-sequencing individual genomes by hybridization.
Chapter 16 Table of Contents Section 1 Genetic Equilibrium
Selectionist view: allele substitution and polymorphism
February 20, 2002 UD, Newark, DE SNPs, Haplotypes, Alleles.
NEW TOPIC: MOLECULAR EVOLUTION.
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,
SNP Comparison Group Members Amira Jhelum Rahul Shweta.
Evolutionary Genome Biology Gabor T. Marth, D.Sc. Department of Biology, Boston College
In populations of finite size, sampling of gametes from the gene pool can cause evolution. Incorporating Genetic Drift.
1 What forces constrain/drive protein evolution? Looking at all coding sequences across multiple genomes can shed considerable light on which forces contribute.
Notes: Human Genome (Right side page)
Published primate genome sequences - I Published primate genome sequences - II.
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.
Inferences on human demographic history using computational Population Genetic models Gabor T. Marth Department of Biology Boston College Chestnut Hill,
Nucleotide variation in the human genome
Learning Target: Evolution of Populations Ch – 11. 2, pp
Gil McVean Department of Statistics
The neutral theory of molecular evolution
Investigating Diversity Part 2
Pipelines for Computational Analysis (Bioinformatics)
The Chimpanzee Genome Motivation for sequencing
Analysis of protein-coding genetic variation in 60,706 humans
Presentation transcript:

Single Nucleotide Polymorphisms (SNPs) By Amira Jhelum Rahul Shweta

Recap of the Project Goal The goal of this project is to compare the distribution of SNPs over certain genes for two different organisms( Humans and Chimpanzees).

Papers to be discussed.. “ Selection on Human Genes as Revealed by Comparisons to Chimpanzee cDNA”. Ines Hellmann, Sebastien Zollener, Wolfgang Enard, Ingo Ebersberger, Birgit Nickel and Svante Paabo

Abstract For better understanding of the evolutionary forces that affect human genes 5055 ESTs were sequenced from the Chimpanzee and compared to the human counterparts Comparison with intergenic Chimpanzee DNA shows that 39% of silent sites in protein coding regions are deletrious and subjected to negative selection

Abstract continued Divergence between human and chimpanzee compared with the extent of nucleotide polymorphisms among humans in same sequences. Positive selection has a considerable influence on 5’ UTRs CpG dinucleotide exhibits a different substitution pattern within 5’UTRs as compared with other parts of the genome.

Highlights of the paper This approach leads towards the understanding of the evolutionary forces that shape the human genome. Chimpanzees differ from humans by an average of 1.2% in overall genomic DNA and are estimated to have shared a common ancestor with humans million years ago. It gives us an insight how the genes have diverged between humans and chimpanzees

Abstract of Paper 2 “ The Essence Of SNPs” By Anthony J.Brookes Single Nucleotide Polymorphisms (SNPs) are abundant forms of genetic variation. Distinguished from rare variations by a requirement for the least abundant allele to have frequency of 1% or more.

Abstract..continued SNP definition and its basics SNP discovery and scoring Population genetics and linkage equilibrium Complex phenotypes and genome variation SNP based association studies The characterization of human SNPs and their role in phenotypic determination represents a truly milestone project, for while humans beings are clearly much more than just “bags of DNA”, perhaps on the individual level we are little more than “sacks of SNPs”.

Paper 3 “Human-Chimpanzee DNA Sequence Variation in the Four Major Genes of the Renin Angiotensin System” Cecile Dufour,Didier Casne, Derek Denten, Jean Wickings, Pierre Corvol and Xavier Jeunemaitre

Abstract The Renin Angiotension System(RAS) is involved in blood pressure control and water/sodium metabolism Genes encoding the proteins of this system are AGT,REN,DCP1 and AGTR1 Observations within and between the four chimpanzees genes oNucleotide diversity at noncoding sites was similar oNucleotide diversity at nonsynonymous sites was low except for the AGT gene o Nucleotide diversity at the synonymous sites, which was dependent upon the G+C content was high except for the AGTR1 gene

Importance of the paper Analysis of the polymorphisms within the species and divergence between species shed light on the evolutionary constraints on the genes Comparison of the pattern of mutation at polymorphic and fixed sites between humans and chimpanzees suggested that the high G+C content of the DCP1 gene was maintained by positive selection at its silent sites 68 ancestral alleles for the human RAS genes are proposed and the implications for their use in future hypertension susceptibility association studies is discussed.

Steps ahead.. Analysis of Chimpanzee and Human data Initial observations and calculations Refining of calculations Biological significance of conclusions and inference

Our website Thank you..