'Disease genes' presentation slideshows

Genome-wide association studies: what they can and can't tell us about disease biology

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Genomics & Medicine http://biochem158.stanford.edu/

Genomics & Medicine http://biochem158.stanford.edu/. Personal Genomics http://biochem158.stanford.edu/Personal%20Genomics.html. The Lancet 2010, 375: 1525-1535. Doug Brutlag Professor Emeritus of Biochemistry & Medicine Stanford University School of Medicine. Low Heritability of Common SNPs.

708 views • 49 slides

Gene Annotation Databases

Genes. Diseases. Diseases. Diseases. Physiology. Diseases. Physiology. Genes. Genes. Anatomy. Diseases. Physiology. Anatomy. Diseases. Physiology. Anatomy. Diseases. Physiology. Anatomy. Diseases. Physiology. Anatomy. Diseases. Physiology. Anatomy. Diseases. Anatomy.

604 views • 47 slides

Gene Annotation Databases

Genes. Diseases. Diseases. Diseases. Physiology. Diseases. Physiology. Genes. Genes. Anatomy. Diseases. Physiology. Anatomy. Diseases. Physiology. Anatomy. Diseases. Physiology. Anatomy. Diseases. Physiology. Anatomy. Diseases. Physiology. Anatomy. Diseases. Anatomy.

508 views • 47 slides

Exome Sequencing as Molecular Diagnostic Tool of Mendelian Diseases

366 views • 36 slides

Array CGH for constitutional disorders: from diagnosis to disease gene discovery

Array CGH for constitutional disorders: from diagnosis to disease gene discovery. Computational Systems Biology. CGH microarrays Molecular karyotyping. Location of chromosomal imbalances. Statistical analysis. Databasing. Validation. Prioritized candidate genes.

595 views • 29 slides

Array CGH for constitutional disorders: from diagnosis to disease gene discovery

Array CGH for constitutional disorders: from diagnosis to disease gene discovery. Computational Systems Biology. CGH microarrays Molecular karyotyping. Location of chromosomal imbalances. Statistical analysis. Databasing. Validation. Prioritized candidate genes.

294 views • 29 slides

LECTURE 19: BIOETHICS AND THE BRAVE NEW WORLD

LECTURE 19: BIOETHICS AND THE BRAVE NEW WORLD. DNA -> RNA -> Protein. X. DNA. Transcription. X. mRNA. X. Translation. Protein. Abnormal Gene Function. Mutations Often Result in the. Synthesis of Abnormal Proteins. Future-Shaping Techologies. Genetic Screening - Marfan Case

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LECTURE 19: BIOETHICS AND THE BRAVE NEW WORLD

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The Human Genetic Disease Network

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Identification and Characterisation of Genes Jo Field Monday 9 th November 2009

Identification and Characterisation of Genes Jo Field Monday 9 th November 2009. Gene identification through knowledge of the gene function Illustrate using examples such as ciliopathies, Fanconi anaemia or HNPCC. Identification and Characterisation of Genes.

368 views • 14 slides

Rationale

Rationale. Need a solid base for analysis of future genomes Reference genome criteria: Sequenced genome MOD Functional genomics projects Adequate research community Sufficient Literature base. Provide broad and deep annotations for reference genomes:

261 views • 9 slides