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These flashcards cover key terms and concepts related to genomes and genomics, derived from the lecture notes.
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Genomics
The study of genomes, including their structure, function, evolution, and mapping.
Whole Genome Sequencing
A method used to determine the complete DNA sequence of an organism's genome.
Bioinformatics
The use of software and computational tools to manage and analyze biological data, particularly genomic data.
Comparative Genomics
The field of biology that compares the genomes of different species to understand their evolutionary relationships.
Functional Genomics
The study of the relationship between genes and their functions or expressions in the context of the genome.
Next-Generation Sequencing
A group of automated techniques used for rapid sequencing of large stretches of DNA, typically resulting in high throughput.
Paired-End Reads
DNA sequencing reads generated from both ends of a DNA fragment, useful for closing gaps in genome assembly.
Open Reading Frame (ORF)
A sequence of DNA that could potentially code for a protein; identified by start and stop codons.
BLAST
Basic Local Alignment Search Tool, a method used to compare an input biological sequence against a database of sequences.
Syntenic Block
Regions of a genome in which the order of genes is conserved across species, providing insights into evolutionary relationships.
Exome Sequencing
The process of sequencing only the coding regions (exons) of a genome, focusing on mutations that impact protein production.
Transposable Elements
DNA sequences that can change their position within the genome, often contributing to genetic variation and evolution.
Pseudogenes
Non-functional segments of DNA that resemble functional genes, often considered evolutionary remnants of functional genes.
Reverse Genetics
An experimental approach used to determine the function of a gene by altering its sequence.
RNAseq
A technique used to analyze the expression of genes through sequencing the RNA in a sample.
Gene Orthologs
Genes in different species that evolved from a common ancestral gene and retain the same function.
Single Nucleotide Polymorphism (SNP)
A variation in a single nucleotide that occurs at a specific position in the genome, which may affect individual traits.
Insertions and Deletions (INDELs)
Genomic variations involving the addition or loss of small segments of DNA, often leading to mutations.