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14 PCA and K-Means Decipher Genome
14 PCA and K-Means Decipher Genome

... The information that is needed for a living cell functioning is encoded in a long molecule of DNA. It can be presented as a text with an alphabet that has only four letters A, C, G and T. The diversity of living organisms and their complex properties is hidden in their genomic sequences. One of the ...
Gene Section RBBP8 (retinoblastoma binding protein 8) Atlas of Genetics and Cytogenetics
Gene Section RBBP8 (retinoblastoma binding protein 8) Atlas of Genetics and Cytogenetics

... development of multiple tumors. Among the types of tumors observed in Ctip+/- animals, B and T cell lymphomas (B-NHL and T-NHL) are most prevalent. Enhanced lymphoid specificity of tumorigenesis might reflect the fact that these tissues are active sites of DNA repair and CtIP insufficiency might con ...
Isolation of a gene encoding a novel chloroplast protein by T
Isolation of a gene encoding a novel chloroplast protein by T

... a 6.85 kb EcoRI fragment of clone GC7 and the strategy used for sequencing of genomic and cDNAs are shown in the lower section and described in Materials and methods. The position of T-DNA insertion in the cs mutant is indicated by a black arrow. 'x' is ORF 'X' located 5' upstream of gene cs. Restri ...
Identification of disease genes by whole genome
Identification of disease genes by whole genome

... Figure 1. From genome profile to disease gene identification. Example of a genome profile obtained by array CGH in a patient with mental retardation and additional congenital malformations. The 32 447 human BAC clones (indicated by small circles representing the log 2-transformed and normalized test ...
BPA leaflet testing and inheritance
BPA leaflet testing and inheritance

... Different porphyrins or porphyrin precursors are permanently raised in each type of porphyria. This is very useful for diagnosis. However, levels of some porphyrins can be raised in anyone, when they are ill. Unfortunately, in the past, tests have checked raised levels of porphyrins without distingu ...
PDF only - at www.arxiv.org.
PDF only - at www.arxiv.org.

... cell-envelope components (5.3%) and cellular processes (4.4%). The nutrient uptake genes acquired through ancient HGT events include ABC transporters for sugars and ribose, glycerol 3-phosphate, spermidine/putrescine, phosphate, zinc and copper. Additionally, Iron permease and Na+/H+ antiporters hav ...
Gene Section JUN (V-Jun sarcoma virus 17 oncogene homolog (avian))
Gene Section JUN (V-Jun sarcoma virus 17 oncogene homolog (avian))

... This work is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 2.0 France Licence. © 2003 Atlas of Genetics and Cytogenetics in Oncology and Haematology ...
Hidden Markov Models in Bioinformatics
Hidden Markov Models in Bioinformatics

... HMMs are perfect for the gene finding task. Categorizing nucleotids within a genomic sequence can be interpreted as a clasification problem with a set of ordered observations that posses hidden structure, that is a suitable problem for the application of hidden Markov models. ...
Page 1 - Mr Waring`s Biology Blog
Page 1 - Mr Waring`s Biology Blog

... The effect of the G and g alleles is modified by another gene. This gene is not sex-linked and it has two alleles. The allele d changes the ginger colour to cream and the black colour to grey. The dominant allele D does not modify the effect of G or g. A cream-coloured male cat mated with a black fe ...
Word file (37 KB )
Word file (37 KB )

... took one sample out and used the remaining 77 samples to define a classifier based on the set of 231 discriminating genes. Then we predicted the outcome of the one sample we left out in the first place. The prediction of the left out sample is based on its correlation coefficient to the “good progno ...
Bioinformatics Analysis of Phenylacetaldehyde Synthase (PAAS), a
Bioinformatics Analysis of Phenylacetaldehyde Synthase (PAAS), a

... or primary structure of a protein is the most important indication for its function. However, it is approved that prediction of protein characteristics from the primary amino acid sequence is not possible directly. Therefore, methods to predict protein characteristics have converged on tertiary and ...
DNA Polymorphisms in the β-lactoglobulin and κ–casein Genes
DNA Polymorphisms in the β-lactoglobulin and κ–casein Genes

... protein variant encoded by allele A than that encoded by allele B. κ-casein gene has been mapped on chromosome 615 in cattle16. The overall length of the κ-casein gene is close to 13 kb, but most of the coding sequences for the ...
Gene list - Bioinformatics.ca
Gene list - Bioinformatics.ca

... if only portion of the total gene complement is queried (or available for annotation), only use that population as background. • To test for enrichment of more than one independent types of annotation (red vs black and circle vs square), apply Fisher’s exact test separately for each type. ***More on ...
TaWRKY70 transcription factor in wheat QTL-2DL regulates
TaWRKY70 transcription factor in wheat QTL-2DL regulates

... resistant cultivars is considered to be the most efficient, economic and environmental friendly method1. More than 200 QTL have been identified, including a total of 52 QTL associated with rachis resistance based on single floret inoculation2. Among these, the QTL-2DL is one of the major and the mos ...
Becker Muscular Dystrophy (BMD)
Becker Muscular Dystrophy (BMD)

... The symptoms of BMD vary greatly from one person to another. Some people lose their ability to walk in early adulthood. Others are able to continue walking throughout their lives. Life expectancy can be reduced, but many people with BMD live into their 70s and 80s. Some may develop heart problems ea ...
UBE3B developmental disorders and increased mortality in cattle
UBE3B developmental disorders and increased mortality in cattle

... of the four variants (rs440561578, rs467377722) segregated also among 191 non-Fleckvieh animals that were sequenced in the context of the 1000 bull genomes project [15] and can be therefore excluded as being causative. In conclusion, only a coding and an intronic variant of the UBE3B gene segregate ...
Request pdf - University of Cambridge
Request pdf - University of Cambridge

... code respectively for about half of TM3 and most of TM4, most of TM5, and all of TM6 and half of TM7, as shown in Fig. 1. The nucleotide and deduced amino acid sequences are shown in Fig. 2, together with the corresponding regions of the human genes (Nathans et al., 1986a). Spectral tuning sequence ...
Martina Šeruga Musić, Mladen Krajačić, Dijana Škorić
Martina Šeruga Musić, Mladen Krajačić, Dijana Škorić

... For direct amplification of phytoplasma gene or pseudogene regions, three different primer pairs were used: 16R738f/16R1232r (GIBB et al., 1995), to amplify a part of 16S rRNA gene; fTufu/rTufu (SCHNEIDER et al., 1997), to amplify a part of tuf gene; and G35p/m (DAVIS et al., 1992), to amplify dnaB ...
Three Genes of the Arabidopsis RPP1 Complex
Three Genes of the Arabidopsis RPP1 Complex

... tomato Cf-9 and Cf-4 R proteins revealed significant sequence divergence only within the N-terminal portion of their LRRs, implicating this domain in specific Avr recognition (Thomas et al., 1997). Molecular analysis of allelic variants at the flax L locus also suggests that the LRR domain is partly ...
Chapter 8
Chapter 8

... bound to binding proteins, and complexes between hnRNA and protein are called heterogeneous ribonucleoprotein particles (hnRNP). Binding proteins function by preventing hnRNA from forming tangled 2˚ structures that would otherwise interfere with processing reactions. As illustrated in Fig. 8.5, many ...
Metatranscriptomic analysis of the Gut microbial community
Metatranscriptomic analysis of the Gut microbial community

... flora. The fermentation of carbohydrates and other nutrients by the gut microbiota on a high fat/high carbohydrate diet can result in an increase SCFA concentration and can result in increased absorption. The SCFA absorbed can promote fat storage via activation of GPR43 and 41 receptors. The presenc ...
The 1B (NS2), 1C (NS1) and N Proteins of Human Respiratory
The 1B (NS2), 1C (NS1) and N Proteins of Human Respiratory

... A 2330 nucleotide sequence spanning tlae 1B (NS2), IC (NS1) and N genes and intergenic regions of human respiratory syncytial virus strain 18537, representing antigenic subgroup B, was determined by sequencing cloned cDNAs of intracellular mRNAs. Comparison with the previously reported sequences for ...
Leukaemia Section 12p abnormalities in myeloid malignancies Atlas of Genetics and Cytogenetics
Leukaemia Section 12p abnormalities in myeloid malignancies Atlas of Genetics and Cytogenetics

... cytogenetic subgroups are defined; deletion in 12p is generally associated with a poor prognosis; however, different clinical courses are defined concerning the magnitude of 12p; a group with small deletions has a better prognosis than patients with 12p abnormalities in general and a lower tendency ...
How do I identify exon number with the UCSC Genome Browser
How do I identify exon number with the UCSC Genome Browser

... How do I identify exon numbers using the UCSC Genome Browser? Let’s visit the browser at genome.ucsc.edu. We will start at this main page and in the upper left-hand corner we will find a couple of links that take us to a location where we can choose our genome of interest. We will click here to rese ...
Continuous Representations of Time Series Gene Expression Data
Continuous Representations of Time Series Gene Expression Data

... Recently, several papers have focused on modeling and analyzing the temporal aspects of gene expression data. In Holter   [10] a time translational matrix is used to model the temporal relationships between different modes of the Singular Value Decomposition (SVD). Unlike our work, this method ...
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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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