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Amsterdam 2004 - Theoretical Biology & Bioinformatics
Amsterdam 2004 - Theoretical Biology & Bioinformatics

... RfbB and RffG catalyze the same reaction, but are involved in two different biological processes. rfb gene cluster: biosynthesis of O-specific polysaccharides (inner membrane). rff gene cluster: complex biosynthesis of enterobacteria common antigen (outer membrane). ...
ppt - Sol Genomics Network
ppt - Sol Genomics Network

...  Potentially generates competition rather than collaboration among groups ...
senior biology - School of Medical Sciences
senior biology - School of Medical Sciences

... Scientists have found more than 1000 different mutations of the CFTR gene; Some have little or no effect on CTFR function, while others cause cystic fibrosis on a spectrum that varies from mild to severe. Click on this link to view a database of all known mutations in the CFTR gene. http://www.gene ...
Methodology for Pattern Discovery, Validation, and Hypothesis
Methodology for Pattern Discovery, Validation, and Hypothesis

... The MADS-box transcription factor AGAMOUS (AG) is an important regulator of stamen and fruit identity as well as floral meristem determinacy in a number of core eudicots and monocots. ...
Understanding protein lists from comparative proteomics studies
Understanding protein lists from comparative proteomics studies

... Vehicle and 5 Aldosterone treated patients. We’ve included only those proteins whose summed spectral counts are >30 in one treatment group. Would it be possible to get the GO annotations for these? The Uniprot name is listed in column A and the gene name is listed in column R. If this is a time cons ...
HM2013058 Research Assistant JD FINAL - Workspace
HM2013058 Research Assistant JD FINAL - Workspace

... acting as a sink for heterochromatin factors and 2) overexpression of genes that escape X chromosome inactivation. Moreover, we have found significant enrichment within the subset of sex chromosome sensitive genes for genes that are also sensitive to the dosage of a key component of heterochromatin ...
Overlapping gene structure of human VLCAD and
Overlapping gene structure of human VLCAD and

... et al., 1999). Since the first two overlapping genes reported by Emi et al. (Emi et al., 1988), a small number of human overlapping genes have been identified (Ubeda et al., 1999; Faurholm et al., 2001; Dan et al., 2002). Although a few cases have been reported, anti-parallel overlapping of exons of ...
Genes 基因
Genes 基因

... Arranged as DNA segments in a chromosome Locus 基因座: specific positions of every gene ...
Ontologies 2 - European Bioinformatics Institute
Ontologies 2 - European Bioinformatics Institute

... • Where an individual gene product that is part of a complex can be annotated to terms that describe the action (function or process) of the whole complex • contributes_to is not needed to annotate a catalytic subunit. ...
Section 7.1: Chromosomes & Phenotypes
Section 7.1: Chromosomes & Phenotypes

... because there is not always two copies of a gene. • Males, only have one chromosome that carries genes (X). • Therefore, for some disorders, a male only needs 1 copy of a gene. • This means males will show all recessive traits because there is no other allele to mask. • In females, their sex-linked ...
PowerPoint - Oregon State University
PowerPoint - Oregon State University

... Mosaics: Groups of cells in the body vary in gene expression ...
Control, Genomes and Environment
Control, Genomes and Environment

Slide 1
Slide 1

... Pleiotropy: One gene ( one protein) controls many phenotypes 40% of cats with white fur and blue eyes are deaf. Marfan syndrome: one gene is responsible for thinness, joint hyper mobility, limb elongation, lens dislocation, and increased susceptibility to ...
Week 3 Genetics - UMK CARNIVORES 3
Week 3 Genetics - UMK CARNIVORES 3

... We know by now that the genome of any life form is made up of many genes. Genes are segments of DNA (some short and some long) that forms the genetic codes (codes for a particular function) for all living things. They are linked together to form very long strands that are packed into what is called ...
ON THE PROBABILITY OF FIXATION OF MUTANT GENES IN A
ON THE PROBABILITY OF FIXATION OF MUTANT GENES IN A

... of a mutant gene for the case of genic selection (i.e. no dominance). Equivalent results have been obtained by HALDANE (1927) and WRIGHT(1931). Also the probability was estimated for a recessive mutant gene by HALDANE (1927) and WRIGHT( 1942). The present author (KIMURA1957) extended these results t ...
Darwinian Reductionism and Genocentrism
Darwinian Reductionism and Genocentrism

... Source of multiple realizability: the operation of natural selection—the biological process par excellence ...
Chp. 2, Section A: Introduction to Inheritance
Chp. 2, Section A: Introduction to Inheritance

... The reason that each of you develop your own unique mixture of family traits is that the pair of genes for each trait that you inherit from your parents often do not have equal effects on your development. For example, as your hair follicles were developing, the gene for curly hair that you got from ...
Genetic Nomenclature
Genetic Nomenclature

... Allele designation is sometimes historical. The name of a gene is often based on mutations for the trait. Cy is the gene for curly wings in Drosophila. Wild-type phenotype is straight wings. w is the gene for white eyes in Drosophila. Wild-type phenotype is brick-red eyes. ...
Mine Microarray Gene Expression Data, Predict Cancers
Mine Microarray Gene Expression Data, Predict Cancers

... • Preference for short trees, and for those with high information gain attributes near the root. • Information is measured with entropy. ...
Chapter 7 Note taking Form
Chapter 7 Note taking Form

... Phenotype is affected by many different factors. *Phenotype can depend on interactions of alleles.  In _____________________ dominance, neither allele is completely dominant nor completely recessive. – _________________________ means that an organism has two different alleles of a gene (___________ ...
CIN_W2_Presentation_Wednesday_Session_1
CIN_W2_Presentation_Wednesday_Session_1

... Singe perturbation experiments even if they indicate causal contribution of gene, assume a fixed genetic background. If there is interaction with the background genes, the results may not be applicable to other contexts. Multifactorial experiments – use existing variation to generate multiple backgr ...
Genetic Nomenclature
Genetic Nomenclature

... Allele designation is sometimes historical. The name of a gene is often based on mutations for the trait. Cy is the gene for curly wings in Drosophila. Wild-type phenotype is straight wings. w is the gene for white eyes in Drosophila. Wild-type phenotype is brick-red eyes. ...
RNAi - University of Maryland, College Park
RNAi - University of Maryland, College Park

... additional copies of a gene encoding a key enzyme for flower pigmentation into petunia plants. When the scientists ended up with fully or partially white flowers they discovered that both types of genes, the endogenous and the newly introduced transgenes, had been turned off. • A few years later pla ...
Application of recombinant DNA technology in protein expression
Application of recombinant DNA technology in protein expression

... protein purification: (Gene fusion strategies) Most target protein lack a suitable Affinity ligand usable for capture on a solid matrix. A way to circumvent this obstacle is to genetically fuse the gene encoding the target protein with a gene encoding a purification tag. When the chimeric protein is ...
PPT - BeeSpace
PPT - BeeSpace

...  10K repositories with > 1K abstracts  (1K with > 10K) ...
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Gene nomenclature

Gene nomenclature is the scientific naming of genes, the units of heredity in living organisms. An international committee published recommendations for genetic symbols and nomenclature in 1957. The need to develop formal guidelines for human gene names and symbols was recognized in the 1960s and full guidelines were issued in 1979 (Edinburgh Human Genome Meeting). Several other species-specific research communities (e.g., Drosophila, mouse) have adopted nomenclature standards, as well, and have published them on the relevant model organism websites and in scientific journals, including the Trends in Genetics Genetic Nomenclature Guide. Scientists familiar with a particular gene family may work together to revise the nomenclature for the entire set of genes when new information becomes available. For many genes and their corresponding proteins, an assortment of alternate names is in use across the scientific literature and public biological databases, posing a challenge to effective organization and exchange of biological information. Standardization of nomenclature thus tries to achieve the benefits of vocabulary control and bibliographic control, although adherence is voluntary. The advent of the information age has brought gene ontology, which in some ways is a next step of gene nomenclature, because it aims to unify the representation of gene and gene product attributes across all species.Gene nomenclature and protein nomenclature are not separate endeavors; they are aspects of the same whole. Any name or symbol used for a protein can potentially also be used for the gene that encodes it, and vice versa. But owing to the nature of how science has developed (with knowledge being uncovered bit by bit over decades), proteins and their corresponding genes have not always been discovered simultaneously (and not always physiologically understood when discovered), which is the largest reason why protein and gene names do not always match, or why scientists tend to favor one symbol or name for the protein and another for the gene. Another reason is that many of the mechanisms of life are the same or very similar across species, genera, orders, and phyla, so that a given protein may be produced in many kinds of organisms; and thus scientists naturally often use the same symbol and name for a given protein in one species (for example, mice) as in another species (for example, humans). Regarding the first duality (same symbol and name for gene or protein), the context usually makes the sense clear to scientific readers, and the nomenclatural systems also provide for some specificity by using italic for a symbol when the gene is meant and plain (roman) for when the protein is meant. Regarding the second duality (a given protein is endogenous in many kinds of organisms), the nomenclatural systems also provide for at least human-versus-nonhuman specificity by using different capitalization, although scientists often ignore this distinction, given that it is often biologically irrelevant.Also owing to the nature of how scientific knowledge has unfolded, proteins and their corresponding genes often have several names and symbols that are synonymous. Some of the earlier ones may be deprecated in favor of newer ones, although such deprecation is voluntary. Some older names and symbols live on simply because they have been widely used in the scientific literature (including before the newer ones were coined) and are well established among users.
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