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Gene Ontology: tool for the unification of biology

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TLDR
The goal of the Gene Ontology Consortium is to produce a dynamic, controlled vocabulary that can be applied to all eukaryotes even as knowledge of gene and protein roles in cells is accumulating and changing.
Abstract
Genomic sequencing has made it clear that a large fraction of the genes specifying the core biological functions are shared by all eukaryotes. Knowledge of the biological role of such shared proteins in one organism can often be transferred to other organisms. The goal of the Gene Ontology Consortium is to produce a dynamic, controlled vocabulary that can be applied to all eukaryotes even as knowledge of gene and protein roles in cells is accumulating and changing. To this end, three independent ontologies accessible on the World-Wide Web (http://www.geneontology.org) are being constructed: biological process, molecular function and cellular component.

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Improved detection of overrepresentation of Gene-Ontology annotations with parent–child analysis

TL;DR: A novel approach to analysis of GO term overrepresentation that determines over representation of terms in the context of annotations to the term's parents is presented, which reduces the dependencies between the individual term's measurements, and thereby avoids producing false-positive results owing to the inheritance problem.
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STITCH 4: integration of protein–chemical interactions with user data

TL;DR: This version of STITCH added features for users to upload their own data to STITCH in the form of internal identifiers, chemical structures or quantitative data, and changed the scheme for transferring interactions between species to rely on orthology rather than protein similarity.
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Quantifying the relationship between co-expression, co-regulation and gene function.

TL;DR: Data from a recent genome wide binding analysis is used in combination with mRNA expression data and existing functional annotations to quantify the likelihood that genes with varying degrees of similarity in mRNA expression profile or function will be bound by a common transcription factor.
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Molecular Signatures of Proliferation and Quiescence in Hematopoietic Stem Cells

TL;DR: The gene expression changes that occur over a time course when hematopoietic stem cells are induced to proliferate and return to quiescence in vivo are examined and a molecular model of the HSC activation cycle is built.
Journal ArticleDOI

Large-scale prediction of Saccharomyces cerevisiae gene function using overlapping transcriptional clusters

TL;DR: This work identifies potential new members of many existing functional categories including 285 candidate proteins involved in transcription, processing and transport of non-coding RNA molecules and presents experimental validation confirming the involvement of several of these proteins in ribosomal RNA processing.
References
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Journal ArticleDOI

Cluster analysis and display of genome-wide expression patterns

TL;DR: A system of cluster analysis for genome-wide expression data from DNA microarray hybridization is described that uses standard statistical algorithms to arrange genes according to similarity in pattern of gene expression, finding in the budding yeast Saccharomyces cerevisiae that clustering gene expression data groups together efficiently genes of known similar function.
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The Pfam protein families database

TL;DR: The definition and use of family-specific, manually curated gathering thresholds are explained and some of the features of domains of unknown function (also known as DUFs) are discussed, which constitute a rapidly growing class of families within Pfam.
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The genome sequence of Drosophila melanogaster

Mark Raymond Adams, +194 more
- 24 Mar 2000 - 
TL;DR: The nucleotide sequence of nearly all of the approximately 120-megabase euchromatic portion of the Drosophila genome is determined using a whole-genome shotgun sequencing strategy supported by extensive clone-based sequence and a high-quality bacterial artificial chromosome physical map.
Journal ArticleDOI

Comprehensive Identification of Cell Cycle–regulated Genes of the Yeast Saccharomyces cerevisiae by Microarray Hybridization

TL;DR: A comprehensive catalog of yeast genes whose transcript levels vary periodically within the cell cycle is created, and it is found that the mRNA levels of more than half of these 800 genes respond to one or both of these cyclins.
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