timeline
... resulting mice, when fed with extra zinc, grow to be huge, and the technique paves the way for a wave of genetic analysis using transgenic mice. ...
... resulting mice, when fed with extra zinc, grow to be huge, and the technique paves the way for a wave of genetic analysis using transgenic mice. ...
GAlibLecture
... // Now create the GA and run it. First we create a genome of the type that // we want to use in the GA. The ga doesn't operate on this genome in the // optimization - it just uses it to clone a population of genomes. //Create the genome object GA1DArrayAlleleGenome genome(leng, range, Objective ...
... // Now create the GA and run it. First we create a genome of the type that // we want to use in the GA. The ga doesn't operate on this genome in the // optimization - it just uses it to clone a population of genomes. //Create the genome object GA1DArrayAlleleGenome
A whole-genome assembly of the domestic cow, Bos taurus
... data file 1 show the number of sequences that had more than a fraction f of their bases contained in each genome for a range of f values. When all alignments of a gene are considered, UMD2 contains at least a portion of 8,659 mRNAs, compared to 8,555 for BCM4. All but two of the genes that map to BC ...
... data file 1 show the number of sequences that had more than a fraction f of their bases contained in each genome for a range of f values. When all alignments of a gene are considered, UMD2 contains at least a portion of 8,659 mRNAs, compared to 8,555 for BCM4. All but two of the genes that map to BC ...
gene (Pun1? - UC Davis Plant Sciences
... • AT3 activity remains to be elucidated – Mutants may identify accumulation of intermediates ...
... • AT3 activity remains to be elucidated – Mutants may identify accumulation of intermediates ...
93134006蔡家妮 期中作業二
... Asia. The 57·3 kb Vibrio pathogenicity island-2 (VPI-2) is confined predominantly to toxigenic V. cholerae O1 and O139 serogroup isolates and encodes 52 ORFs (VC1758 to VC1809), which include homologues of an integrase (VC1758), a restriction modification system, a sialic acid metabolism gene cluste ...
... Asia. The 57·3 kb Vibrio pathogenicity island-2 (VPI-2) is confined predominantly to toxigenic V. cholerae O1 and O139 serogroup isolates and encodes 52 ORFs (VC1758 to VC1809), which include homologues of an integrase (VC1758), a restriction modification system, a sialic acid metabolism gene cluste ...
repetitive extragenic palindromic sequences in pseudomonas
... conserved palindromy of REP sequences and the conserved arrangement of the clusters it is probable that REP sequences adopt conformations with peculiar secondary structures especially suitable to be specifically recognized by proteins. REP sequences are binding sites for proteins such as IHF, HU, gy ...
... conserved palindromy of REP sequences and the conserved arrangement of the clusters it is probable that REP sequences adopt conformations with peculiar secondary structures especially suitable to be specifically recognized by proteins. REP sequences are binding sites for proteins such as IHF, HU, gy ...
Functional and ecological impacts of horizontal gene transfer in
... environments is well known. This is exemplified by the high level of HGT observed in the genome of the thermoacidophile Thermotoga, which has acquired genes relating to its environment and metabolism from archaebacteria inhabiting similar environments [30,31]. The possible role of HGT in adapting to ...
... environments is well known. This is exemplified by the high level of HGT observed in the genome of the thermoacidophile Thermotoga, which has acquired genes relating to its environment and metabolism from archaebacteria inhabiting similar environments [30,31]. The possible role of HGT in adapting to ...
Microdeletions on the long arm of the Y chromosome
... in the AZFc region.16 Originally thought to be a single-copy gene, DAZ is now known to be a multicopy gene family, which includes DAZ2, formerly known as spermatogenesis gene on Y (SPGY),13 and its autosomal copy on the short arm of chromosome 3 (DAZL1).13 The DAZ genes are expressed exclusively in ...
... in the AZFc region.16 Originally thought to be a single-copy gene, DAZ is now known to be a multicopy gene family, which includes DAZ2, formerly known as spermatogenesis gene on Y (SPGY),13 and its autosomal copy on the short arm of chromosome 3 (DAZL1).13 The DAZ genes are expressed exclusively in ...
The Complete Chloroplast and Mitochondrial DNA Sequence of
... immediate ancestors, a group of algae known as ‘‘charophyte green algae’’ (e.g., Chaetosphaeridium globosum), whereas Chlorophyta contain the other green algae (e.g., Chlamydomonas reinhardtii) that form a monophyletic assemblage and are a sister group to the Streptophyta (Graham and Wilcox 2000). S ...
... immediate ancestors, a group of algae known as ‘‘charophyte green algae’’ (e.g., Chaetosphaeridium globosum), whereas Chlorophyta contain the other green algae (e.g., Chlamydomonas reinhardtii) that form a monophyletic assemblage and are a sister group to the Streptophyta (Graham and Wilcox 2000). S ...
What can whole genome expression data tell us about the ecology
... a large number of genes, and is an attractive approach for studying personality because behavioural traits are often polygenic, sensitive to the environment and subject to epistatic interactions. Furthermore, a growing number of studies are showing that gene regulation is often correlated with pheno ...
... a large number of genes, and is an attractive approach for studying personality because behavioural traits are often polygenic, sensitive to the environment and subject to epistatic interactions. Furthermore, a growing number of studies are showing that gene regulation is often correlated with pheno ...
Conservation of gene function in behaviour
... still others are found in some but not all species. Nevertheless, similar to well-known examples in evodevo, we can conclude that the structure of the molecular mechanism underlying clocks is similar in both groups. The genes involved are highly conserved at the DNA level, and some genes function in ...
... still others are found in some but not all species. Nevertheless, similar to well-known examples in evodevo, we can conclude that the structure of the molecular mechanism underlying clocks is similar in both groups. The genes involved are highly conserved at the DNA level, and some genes function in ...
Intermediate Alleles - Huntington Society of Canada
... HD later in life. Children are at-risk of developing HD later in life because the number of CAG repeats may increase when the IA is passed from parent to child. If the number of CAG repeats increases to 36 or more, the child will develop HD in their lifetime. Scientists call this increase in the num ...
... HD later in life. Children are at-risk of developing HD later in life because the number of CAG repeats may increase when the IA is passed from parent to child. If the number of CAG repeats increases to 36 or more, the child will develop HD in their lifetime. Scientists call this increase in the num ...
Computational Biology
... (e.g. level of conservation of amino acids) of individual genes/proteins. Genetic distance is defined as # mismatches / # matches. Sequence conservation depends on physico-chemical properties of amino acids (and genome context such as G+C content). ...
... (e.g. level of conservation of amino acids) of individual genes/proteins. Genetic distance is defined as # mismatches / # matches. Sequence conservation depends on physico-chemical properties of amino acids (and genome context such as G+C content). ...
Red Line Walk-through
... translated into amino acid sequences. UniGene: A database of transcript data, “each UniGene entry is a set of transcript sequences that appear to come from the same transcription locus (gene or expressed pseudogene), together with information on protein similarities, gene expression, cDNA clone reag ...
... translated into amino acid sequences. UniGene: A database of transcript data, “each UniGene entry is a set of transcript sequences that appear to come from the same transcription locus (gene or expressed pseudogene), together with information on protein similarities, gene expression, cDNA clone reag ...
Selective regain of egfr gene copies in CD44+/CD24
... cause and promoter of cancer progression or if distinct DNA sequence mutations have to lead the way. Clonal selection during cancer development may lead to a dominant cancer cell subpopulation with distinct chromosomal alterations. But, in most cases a heterogeneous cell population can be found with ...
... cause and promoter of cancer progression or if distinct DNA sequence mutations have to lead the way. Clonal selection during cancer development may lead to a dominant cancer cell subpopulation with distinct chromosomal alterations. But, in most cases a heterogeneous cell population can be found with ...
Document
... from a single gene multiple transcripts) AS is tissue-specific (Graveley, 2001) AS is related to human diseases ...
... from a single gene multiple transcripts) AS is tissue-specific (Graveley, 2001) AS is related to human diseases ...
An Investigation Into the Relationship Between Taq1 and Apa1
... in the development of OA. The results of the present study indicated that the percentage of allele frequencies and the distribution of genotypes of the VDR gene TaqI and ApaI polymorphisms were not significantly different when analyzing the OA patients and the controls. Moreover, there was no associ ...
... in the development of OA. The results of the present study indicated that the percentage of allele frequencies and the distribution of genotypes of the VDR gene TaqI and ApaI polymorphisms were not significantly different when analyzing the OA patients and the controls. Moreover, there was no associ ...
Cowboy Genetics
... of information on lots of generations and based on the data we have, we can make assumptions about inheritance of the defective genes. Mapping Looking for a defective gene depends upon a couple of “genetic laws.” The idea here is when cells split (to form embryos and eventually baby bovines), some p ...
... of information on lots of generations and based on the data we have, we can make assumptions about inheritance of the defective genes. Mapping Looking for a defective gene depends upon a couple of “genetic laws.” The idea here is when cells split (to form embryos and eventually baby bovines), some p ...
Diapositive 1 - Institut Pasteur
... – Unicellular eukaryotes genome databases – Fungal genome databases – Invertebrate genome databases ...
... – Unicellular eukaryotes genome databases – Fungal genome databases – Invertebrate genome databases ...
Origin of the eukaryotic cell
... The discovery of 2.1 billion years old Eukaryotic fossils in Gabon July 2010 has brought new insights into the origin of eukaryotic cell (Albani et al. 2010). The relationship among three domains, Eukaryotes, Bacteria and Archaea, in the tree of life was investigated in this project through phylogen ...
... The discovery of 2.1 billion years old Eukaryotic fossils in Gabon July 2010 has brought new insights into the origin of eukaryotic cell (Albani et al. 2010). The relationship among three domains, Eukaryotes, Bacteria and Archaea, in the tree of life was investigated in this project through phylogen ...
Ch. 7: Presentation Slides
... • When chromosome 21 is one of the acrocentrics in a Robertsonian translocation, the rearrangement leads to a familial type of Down syndrome • The heterozygous carrier is phenotypically normal, but a high risk of Down syndrome results from aberrant segregation in meiosis • Approximately 3 percent of ...
... • When chromosome 21 is one of the acrocentrics in a Robertsonian translocation, the rearrangement leads to a familial type of Down syndrome • The heterozygous carrier is phenotypically normal, but a high risk of Down syndrome results from aberrant segregation in meiosis • Approximately 3 percent of ...
Genomic Gene Clustering Analysis of Pathways
... genes were found in uber-operons as well. Lathe et al. (2000) showed that uber-operons can be used to correctly predict function of ‘hypothetical’ proteins. Operons that have been detected in eukaryotes differ from those in prokaryotes in that eukaryotic polycistronic mRNAs are not translatable dire ...
... genes were found in uber-operons as well. Lathe et al. (2000) showed that uber-operons can be used to correctly predict function of ‘hypothetical’ proteins. Operons that have been detected in eukaryotes differ from those in prokaryotes in that eukaryotic polycistronic mRNAs are not translatable dire ...
The Effect of a Coat Colour-Associated Genes Polymorphism on
... In horses the KIT gene is also the candidate gene for roan coat colour (Marklund et al., 1999). Horses of roan phenotype are characterized by grey coat colour that results from blending the basic colour with white bristles in the thorax, neck, and partially limb areas. Roan coat colour in horses is ...
... In horses the KIT gene is also the candidate gene for roan coat colour (Marklund et al., 1999). Horses of roan phenotype are characterized by grey coat colour that results from blending the basic colour with white bristles in the thorax, neck, and partially limb areas. Roan coat colour in horses is ...
Copy-number variation
Copy-number variations (CNVs)—a form of structural variation—are alterations of the DNA of a genome that results in the cell having an abnormal or, for certain genes, a normal variation in the number of copies of one or more sections of the DNA. CNVs correspond to relatively large regions of the genome that have been deleted (fewer than the normal number) or duplicated (more than the normal number) on certain chromosomes. For example, the chromosome that normally has sections in order as A-B-C-D might instead have sections A-B-C-C-D (a duplication of ""C"") or A-B-D (a deletion of ""C"").This variation accounts for roughly 13% of human genomic DNA and each variation may range from about one kilobase (1,000 nucleotide bases) to several megabases in size. CNVs contrast with single-nucleotide polymorphisms (SNPs), which affect only one single nucleotide base.