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\documentclass{article}
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\usepackage[margin = 1in]{geometry}
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\usepackage{hyperref}
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\hypersetup{colorlinks = TRUE, citecolor=blue}
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\usepackage{amsmath}
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\usepackage{amssymb}
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\usepackage{graphicx}
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\usepackage[export]{adjustbox}
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\usepackage{natbib}
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\linespread{2}
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\usepackage{indentfirst}
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\begin{document}
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\section{?All models are wrong. Some models are useful. (George Box)}
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\section{Introduction to Genomics}
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\subsection{What is DNA?}
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% first concepts to define: DNA, gene, expression
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% what genes do
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\subsection{Common Misconceptions}
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DNA does not define everything about you.
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- which genes are "turned on/off"
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- different upbringings and environments
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\subsection{(Define Jargon) Genomic Variation}
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\subsection{Why study Genomic Variation?}
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- Important for health and precision medicine
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- Catalogs different ways in which people's genomes are healthy.
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- When looking for disease-related genomic variants, we can use this information to rule out healthy variants.
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\subsection{Natural Selection}
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Thus, a variant that occurs naturally in a population likely doesn't cause disease symptoms.
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\subsection{(Define Jargon) SNPs}
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Single Nucleotide Polymorphism
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poly- many
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morph - 
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Why SNP data ?
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\subsection{Data (vcf file)}
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\end{document}