Tandem Genetic Duplications in Phage and Bacteria
... join point between copies of the duplicated segment. At this point, sequences that would be widely separated in a normal chromosome are made contiguous. Trans duction of this join point from a donor harboring a duplication into a normal recipient may have surprising results. It is possible to reest ...
... join point between copies of the duplicated segment. At this point, sequences that would be widely separated in a normal chromosome are made contiguous. Trans duction of this join point from a donor harboring a duplication into a normal recipient may have surprising results. It is possible to reest ...
Molecular Mapping of D1, D2 and ms5 Revealed Linkage
... The mutant is inherited as a single-gene recessive trait; however, no cytological studies have been conducted. The cotyledon color trait in soybean is controlled by two loci: D1 and D2 [29,30]. Carter and Burton [31] discovered an association between the green cotyledon trait and the ms5 locus. Due ...
... The mutant is inherited as a single-gene recessive trait; however, no cytological studies have been conducted. The cotyledon color trait in soybean is controlled by two loci: D1 and D2 [29,30]. Carter and Burton [31] discovered an association between the green cotyledon trait and the ms5 locus. Due ...
Genetics Dihybrid
... which he used peas that differed from each other in two traits rather than only one. ...
... which he used peas that differed from each other in two traits rather than only one. ...
Thrombocytopenia-absent radius (TAR) syndrome due to compound
... can be at the basis of recurrent DNA rearrangements such as deletions, duplications and inversions through chromosome or chromatid misalignment followed by non-allelic homologous recombination (NAHR) [13–15]. TAR syndrome has a complex pattern of inheritance associated with a minimal common intersti ...
... can be at the basis of recurrent DNA rearrangements such as deletions, duplications and inversions through chromosome or chromatid misalignment followed by non-allelic homologous recombination (NAHR) [13–15]. TAR syndrome has a complex pattern of inheritance associated with a minimal common intersti ...
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... polymorphism (T-RFLP) analysis of 16S rRNA genes and the nucleotide sequence responsible for each terminal restriction fragment (T-RF) was determined by 16S rRNA gene cloning and sequencing [18]. Two major populations, one assigned to the genus Thauera, and another related to the genera Ralstonia an ...
... polymorphism (T-RFLP) analysis of 16S rRNA genes and the nucleotide sequence responsible for each terminal restriction fragment (T-RF) was determined by 16S rRNA gene cloning and sequencing [18]. Two major populations, one assigned to the genus Thauera, and another related to the genera Ralstonia an ...
Lin, R., C. D. Allis and S. J. Elledge. 1996. PAT1
... between chH1 and lacZ (data not shown). A genetic screen was performed to identify mutants whose growth is dependent on the expression of chH1. These mutants are expected to be defective either in the yeast histone H1 homologue or other genes that are suppressible by chicken H1 protein. Cells with l ...
... between chH1 and lacZ (data not shown). A genetic screen was performed to identify mutants whose growth is dependent on the expression of chH1. These mutants are expected to be defective either in the yeast histone H1 homologue or other genes that are suppressible by chicken H1 protein. Cells with l ...
The vertebrate genome annotation (Vega) database
... Mouse diabetes (IDD) candidate regions. Mouse strain NOD (non-obese diabetic) is a model for identifying genes involved in IDD (insulin-dependent diabetes) (12–14). We are annotating candidate regions, in parallel, in the reference BL/6 strain and the NOD strain in order to compare the two strains a ...
... Mouse diabetes (IDD) candidate regions. Mouse strain NOD (non-obese diabetic) is a model for identifying genes involved in IDD (insulin-dependent diabetes) (12–14). We are annotating candidate regions, in parallel, in the reference BL/6 strain and the NOD strain in order to compare the two strains a ...
A String-based Model for Simple Gene Assembly
... assembly on legal strings is equivalent to that on signed permutations. Legal strings have been used before to formalise the general operations in [2]. This definition is missing one crucial piece of information, necessary to model simple operations in particular. Namely, the absence of markers indi ...
... assembly on legal strings is equivalent to that on signed permutations. Legal strings have been used before to formalise the general operations in [2]. This definition is missing one crucial piece of information, necessary to model simple operations in particular. Namely, the absence of markers indi ...
Involvement of HLS1 in Sugar and Auxin
... hls1-7 transcripts were higher than that of the wild type, suggesting that HLS1 is subject to negative feedback regulation. A decrease in HLS1/hls1 transcripts by the presence of Suc was observed only in hls1 mutants, indicating that HLS1 is a conditional sugar-repressed gene only when Suc sensitivi ...
... hls1-7 transcripts were higher than that of the wild type, suggesting that HLS1 is subject to negative feedback regulation. A decrease in HLS1/hls1 transcripts by the presence of Suc was observed only in hls1 mutants, indicating that HLS1 is a conditional sugar-repressed gene only when Suc sensitivi ...
Incomplete Dominance Codominance Multiple alleles and lethal
... Incomplete dominance is different and involves a mixing of the two traits to form an intermediate variety. To the side you see the red flower which is homozygous RR and the white flower which is homozygous ww. Heterozygote is pink Rw in-between two ...
... Incomplete dominance is different and involves a mixing of the two traits to form an intermediate variety. To the side you see the red flower which is homozygous RR and the white flower which is homozygous ww. Heterozygote is pink Rw in-between two ...
A program for annotating and predicting the effects of single
... genome sequences. Once a genome is sequenced, the SnpEff program can be used to annotate and classify genetic polymorphisms based on their effects on annotated genes, such as synonymous or non-synonymous SNPs, start codon gains or losses, stop codon gains or losses; or based on their genomic locatio ...
... genome sequences. Once a genome is sequenced, the SnpEff program can be used to annotate and classify genetic polymorphisms based on their effects on annotated genes, such as synonymous or non-synonymous SNPs, start codon gains or losses, stop codon gains or losses; or based on their genomic locatio ...
Project name
... The software was developed using the Microsoft Visual studio; an integrated Development Environment (IDE) with the in-built programming language C#. The system was developed as a console program On initialisation of the software, random chromosomes are generated and the system locates the dataset fi ...
... The software was developed using the Microsoft Visual studio; an integrated Development Environment (IDE) with the in-built programming language C#. The system was developed as a console program On initialisation of the software, random chromosomes are generated and the system locates the dataset fi ...
Familial spontaneous pneumothorax and mutation CASE STUDY
... mutations on exon 4 [5] and exons 9 and 12 [6]. It is possible that these regions (and exon 10) encode functional domains particularly relevant to lung development. It is interesting to note that, among patients with mutations in the exon 11 hotspot, significantly fewer renal tumours were observed i ...
... mutations on exon 4 [5] and exons 9 and 12 [6]. It is possible that these regions (and exon 10) encode functional domains particularly relevant to lung development. It is interesting to note that, among patients with mutations in the exon 11 hotspot, significantly fewer renal tumours were observed i ...
Gene Section TP53 (tumor protein p53 (Li-Fraumeni syndrome)) in Oncology and Haematology
... non-mutated allele is generally lost. The frequency and the type of mutation may vary from one tumour type to another. Somatic TP53 mutations are frequent in most human cancers, ranging from 5% to 80% depending on the type, stage and etiology of tumors. Most mutations are missense (75%) and other in ...
... non-mutated allele is generally lost. The frequency and the type of mutation may vary from one tumour type to another. Somatic TP53 mutations are frequent in most human cancers, ranging from 5% to 80% depending on the type, stage and etiology of tumors. Most mutations are missense (75%) and other in ...
Genetic evaluation of suspected osteogenesis imperfecta (OI)
... loss and joint laxity.1 The severity ranges from lethal in the perinatal period to occasional fracture. Inheritance is generally autosomal dominant but new mutations are common and recessive inheritance occurs. In most instances (about 90%), a mutation in one of the two genes (COL1A1 and COL1A2) tha ...
... loss and joint laxity.1 The severity ranges from lethal in the perinatal period to occasional fracture. Inheritance is generally autosomal dominant but new mutations are common and recessive inheritance occurs. In most instances (about 90%), a mutation in one of the two genes (COL1A1 and COL1A2) tha ...
Codon bias domains over bacterial chromosomes
... Selection based on the rarity of the codon in the host genome is slightly significant (p=0.018 before Bonferroni correction) Selection based on the difference of frequencies of codon usage between phage and host is highly significant (p<2.10-7) The tRNA duplication hypothesis has to be rejected ...
... Selection based on the rarity of the codon in the host genome is slightly significant (p=0.018 before Bonferroni correction) Selection based on the difference of frequencies of codon usage between phage and host is highly significant (p<2.10-7) The tRNA duplication hypothesis has to be rejected ...
Ellis–van Creveld syndrome - RJME
... genome and the two genes could be coordinated by the same promotor or shared elements of overlapping promoters, so, mutations of any of these genes emerge to the same phenotype [1]. The murine and bovine orthologue of EVC2, LBN which codes for limbin is strongly expressed in proliferating condrocyte ...
... genome and the two genes could be coordinated by the same promotor or shared elements of overlapping promoters, so, mutations of any of these genes emerge to the same phenotype [1]. The murine and bovine orthologue of EVC2, LBN which codes for limbin is strongly expressed in proliferating condrocyte ...
Part 1: PCA & MDS COS 323
... • Formally, let’s say we have n × n matrix D consisting of squared distances dij = (xi – xj)2 • Want to recover n × k matrix X of positions in k-dimensional space ...
... • Formally, let’s say we have n × n matrix D consisting of squared distances dij = (xi – xj)2 • Want to recover n × k matrix X of positions in k-dimensional space ...
Arabidopsis thaliana: A Model Plant for Genome Analysis
... Arabidopsis thaliana has recently become the organism of choice for a wide range of studies in plant sciences (1). The current visibility of Arabidopsis research reflects the growing realization among biologists that this simple angiosperm can serve as a convenient model not only for plant biology b ...
... Arabidopsis thaliana has recently become the organism of choice for a wide range of studies in plant sciences (1). The current visibility of Arabidopsis research reflects the growing realization among biologists that this simple angiosperm can serve as a convenient model not only for plant biology b ...
Application of a Real Time Polymerase Chain Reaction Method to
... observed in the assay when the template was genomic DNA extracted from the unspiked milk and egg samples. To confirm the presence of DNA in the unspiked food samples, PCR assays were performed to amplify the 18S rRNA gene using DNA templates extracted from spiked and unspiked milk and egg samples. P ...
... observed in the assay when the template was genomic DNA extracted from the unspiked milk and egg samples. To confirm the presence of DNA in the unspiked food samples, PCR assays were performed to amplify the 18S rRNA gene using DNA templates extracted from spiked and unspiked milk and egg samples. P ...
Interval mapping of QTLs controlling yield
... The garden pea (Pisum sativum L.) is one of the most important legume crops in Europe. The majority of agriculturally significant traits in pea, as in other plant species, are inherited quantitatively. The complexity of these phenotypic traits exhibiting continuous variation arises from the segregat ...
... The garden pea (Pisum sativum L.) is one of the most important legume crops in Europe. The majority of agriculturally significant traits in pea, as in other plant species, are inherited quantitatively. The complexity of these phenotypic traits exhibiting continuous variation arises from the segregat ...
Extensive tRNA gene changes in synthetic Brassica
... tRNA genes rather than entire tRNA genes. From in silico mapping, these sequences were located across 9/10 chromosomes of B. rapa (all but A6) and all 9 chromosomes of B. oleracea. Using these sequences, 46 tRNA genes formed by 16 tRNA types in 45 homologous sequences (64.3%) were predicted by the t ...
... tRNA genes rather than entire tRNA genes. From in silico mapping, these sequences were located across 9/10 chromosomes of B. rapa (all but A6) and all 9 chromosomes of B. oleracea. Using these sequences, 46 tRNA genes formed by 16 tRNA types in 45 homologous sequences (64.3%) were predicted by the t ...
AA - Virginia Institute for Psychiatric and Behavioral Genetics
... Dizygotic (DZ, “fraternal” or “nonidentical”): result from independent fertilization of two eggs by two sperm; share on average 50% of their genes ...
... Dizygotic (DZ, “fraternal” or “nonidentical”): result from independent fertilization of two eggs by two sperm; share on average 50% of their genes ...