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Related Concept Videos

Genome Annotation and Assembly03:36

Genome Annotation and Assembly

The genome refers to all of the genetic material in an organism. It can range from a few million base pairs in microbial cells to several billion base pairs in many eukaryotic organisms. Genome assembly refers to the process of taking the DNA sequencing data and putting it all back together in a correct order to create a close representation of the original genome. This is followed by the identification of functional elements on the newly assembled genome, a process called genome annotation.
Genomics02:02

Genomics

Genomics is the science of genomes: it is the study of all the genetic material of an organism. In humans, the genome consists of information carried in 23 pairs of chromosomes in the nucleus, as well as mitochondrial DNA. In genomics, both coding and non-coding DNA is sequenced and analyzed. Genomics allows a better understanding of all living things, their evolution, and their diversity. It has a myriad of uses: for example, to build phylogenetic trees, to improve productivity and...
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Oligosaccharide Assembly

Protein glycosylation starts in the ER lumen and continues in the Golgi apparatus. Glycosyltransferases catalyze the addition of sugar molecules or glycosylation of proteins. Usually, these enzymes add sugars to the hydroxyl groups of selected serine or threonine residues to form O-linked glycans or the amino groups of asparagine residues to form N-linked glycans. Different positions on the same polypeptide chain can contain differently linked glycans.
Multiple sugar molecules that may or may...
RNA-seq03:21

RNA-seq

RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases. 
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Genome-wide Association Studies-GWAS01:11

Genome-wide Association Studies-GWAS

Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
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Genome Size and the Evolution of New Genes03:21

Genome Size and the Evolution of New Genes

While every living organism has a genome of some kind (be it RNA, or DNA), there is considerable variation in the sizes of these blueprints. One major factor that impacts genome size is whether the organism is prokaryotic or eukaryotic. In prokaryotes, the genome contains little to no non-coding sequence, such that genes are tightly clustered in groups or operons sequentially along the chromosome. Conversely, the genes in eukaryotes are punctuated by long stretches of non-coding sequence.

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Development of Compendium for Esophageal Squamous Cell Carcinoma
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Gene Ontology annotations at SGD: new data sources and annotation methods.

Eurie L Hong1, Rama Balakrishnan, Qing Dong

  • 1Department of Genetics, Stanford University, Stanford, CA, USA.

Nucleic Acids Research
|November 6, 2007
PubMed
Summary

The Saccharomyces Genome Database now integrates high-throughput experiments and computational predictions for yeast gene products. This expansion enhances Gene Ontology annotations, especially for uncharacterized genes, improving data accuracy and completeness.

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Area of Science:

  • Yeast genomics and bioinformatics
  • Functional genomics and annotation
  • Computational biology

Background:

  • The Saccharomyces Genome Database (SGD) is a primary resource for budding yeast Saccharomyces cerevisiae information.
  • Gene Ontology (GO) annotations traditionally rely on published experimental data.
  • High-throughput experiments and computational predictions offer valuable data, particularly for understudied genes.

Purpose of the Study:

  • To enhance the Saccharomyces Genome Database (SGD) with diverse data sources for Gene Ontology (GO) annotations.
  • To distinguish between different data sources and annotation methods within SGD.
  • To improve the comprehensiveness and accuracy of GO annotations for yeast genes.

Main Methods:

  • Integration of high-throughput experimental data into SGD.
  • Inclusion of computational predictions from the GO Annotation Project (GOA UniProt).
  • Modification of SGD resources to differentiate annotation sources and methods.

Main Results:

  • SGD now provides GO annotations derived from high-throughput data and computational predictions.
  • SGD resources are updated to clearly indicate the origin and type of GO annotation data.
  • Enhanced ability to compare SGD annotations with independent sources.

Conclusions:

  • The expanded SGD GO annotation resource offers a more complete view of yeast gene functions.
  • Distinguishing data sources aids users in evaluating annotation evidence.
  • The integrated data supports ongoing curation and identification of novel gene functions.