'Disease gene' presentation slideshows

Introduction and Framework

Introduction and Framework. INLS 541: Information Visualization Brad Hemminger. What do you know about visualizations?. Name some types of visualizations? When did they first appear? . William Playfair : the first data chart.

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Sequencing the Human Genome

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Linkage Analysis I -- Parametric

Linkage Analysis I -- Parametric . 2006.3.3 I-Ping Tu. Book reference. http://www.math.chalmers.se/Stat/Grundutb/Chalmers/TMS120/kompendium.pdf Genetic Linkage Web Resource: http://linkage.rockefeller.edu/. 1 Introduction. Quality Trait: e.g. tall/short, green/yellow,

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Introduction Center for Medical Genetics

Introduction Center for Medical Genetics. Staff (81) Clinicians and psychologists Laboratory supervisors Researchers Laboratory technicians Secretary. Introduction Center for Medical Genetics. Diagnosis of genetic disorders Clinical assesment Laboratory investigations (three labs)

1.05k views • 75 slides

Linkage Analysis

Linkage Analysis. Eric Jorgenson Epidemiology 217 2/26/13. Worldwide Distribution of Human Earwax SNP rs17822931. Yoshiura et al., Nature Genetics 2006. Geographic Distribution of PTC Phenotype. High. Low. Wooding Genetics 2006, adapted from Cavalli-Sforza 1994.

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Linkage Analysis

Linkage Analysis. Eric Jorgenson Epidemiology 217 2/21/12. Worldwide Distribution of Human Earwax SNP rs17822931. Yoshiura et al., Nature Genetics 2006. Geographic Distribution of PTC Phenotype. High. Low. Wooding Genetics 2006, adapted from Cavalli-Sforza 1994.

764 views • 62 slides

Linkage Analysis

Linkage Analysis. Eric Jorgenson EPI 217 1/25/11. More taste strips. One long One short. Bimodal Distribution of PTC. Types of Genetic Studies. Family Studies Compare trait values across family members Linkage Analysis Compare trait values with inheritance patterns Association

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Recombination and Linkage

Recombination and Linkage. The genetic approach. Start with the phenotype; find genes the influence it. Allelic differences at the genes result in phenotypic differences. Value: Need not know anything in advance. Goal Understanding the disease etiology (e.g., pathways)

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CSE280b: Population Genetics

CSE280b: Population Genetics. Vineet Bafna/Pavel Pevzner. www.cse.ucsd.edu/classes/sp05/cse291. Review. Hardy Weinberg Equilibrium Linkage Equlibrium. Recombination and Linkage Equilibrium.

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Medical Biotechnology

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Alcohol & other addictions: can DNA make a difference?

Alcohol & other addictions: can DNA make a difference?. Dr Martin Kennedy Department of Pathology Christchurch School of Medicine & Health Sciences University of Otago. Topics:. Genes 101 Complex disorders 101 Are there genes for addiction? What might they do? How will we find them?

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Gene mapping: Linkage and association methods

Disease gene mapping is one of the main purposes for genotyping Two major approaches: linkage and association analyses. Gene mapping: Linkage and association methods. Try to localize genes affecting specific phenotypes Search for: co-segregation of disease and marker alleles.

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Human Gene Mapping and Disease Gene Identificaton

Human Gene Mapping and Disease Gene Identificaton. Paul Coucke Jan Hellemans Andy Willaert. 10. Chapter. Chapter 10. The genetic landscape of the human genome Mapping human genes by linkage analysis Mapping of complex traits From gene mapping to gene identification. Aims.

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Genomics, Cancers & Infectious Diseases

Genomics, Cancers & Infectious Diseases. Qunyuan Zhang Division of Statistical Genomics Washington University School of Medicine. Genomes Sequenced. 1995: H. influenzae, the first sequenced genome of a free-living organism 2011: 11554 bacterial genomes

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GENETIC DISEASE

BIOCHEMISTRY

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Genetics of Parkinson

Genetics of Parkinson. Carlos Singer MD Professor of Neurology Chief, Division of Parkinson and Movement Disorders University of Miami Leonard M. Miller School of Medicine May 20, 2010

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Mapping of Simple & Complex Genetic Diseases

Mapping of Simple & Complex Genetic Diseases. Anne Haake Rhys Price Jones. Simple Diseases. Follow Mendelian inheritance patterns e.g. autosomal dominant, x-linked recessive Generally rare Caused by changes in one gene Examples: Cystic Fibrosis, Duchenne Muscular Dystrophy.

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Extension of disease-related pathway using text mining

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Huntington Disease - The Most Common Hereditary Brain Disorders

Huntington disease is an autosomal dominant disorder, meaning that a person needs one copy of the defective gene to develop the disorder.

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Possible ways of synthetic analysis in H-Inv Disease Edition

Literature (PubMed). Possible ways of synthetic analysis in H-Inv Disease Edition. Specific disease. Select specific disease. Known disease gene. List of genes. Genomic region of interest (GROI). Dictionary. Scoring system (PANDA). Text-mining. H-InvDB Other DB.

157 views • 1 slides