Analysis of Drosophila Species Genome Size and Satellite DNA
... elements typical of heterochromatin, may have repeatspecific shrinkage mechanisms, such as unequal meiotic exchange between sister chromatids or replication errors (Britten and Kohne 1968; Southern 1975; Smith 1976; Stephan and Cho 1994; Petrov 2001). Understanding the levels and distributions of he ...
... elements typical of heterochromatin, may have repeatspecific shrinkage mechanisms, such as unequal meiotic exchange between sister chromatids or replication errors (Britten and Kohne 1968; Southern 1975; Smith 1976; Stephan and Cho 1994; Petrov 2001). Understanding the levels and distributions of he ...
sex-linked hybrid sterility in a butterfly - Ziheng Yang
... and female sterility are not the same, we do not necessarily expect that an X chromosome carrying male sterility loci will also contain female sterility loci (Turelli and Orr 1995; Orr 1997). There is now convincing evidence from Drosophila that loci causing hybrid inviability act in both sexes, whe ...
... and female sterility are not the same, we do not necessarily expect that an X chromosome carrying male sterility loci will also contain female sterility loci (Turelli and Orr 1995; Orr 1997). There is now convincing evidence from Drosophila that loci causing hybrid inviability act in both sexes, whe ...
How to report IG sequence data in clinical Richard Rosenquist Uppsala, Sweden
... Multiple rearrangements • 1.5% of cases carried double productive rearrangements (Murray et al, Blood 2008). • More frequent when using gDNA. • Usually only one rearrangement transcribed, however: – Allelic exclusion or ’allelic inclusion’ has been described. ...
... Multiple rearrangements • 1.5% of cases carried double productive rearrangements (Murray et al, Blood 2008). • More frequent when using gDNA. • Usually only one rearrangement transcribed, however: – Allelic exclusion or ’allelic inclusion’ has been described. ...
19p13.3 microdeletions
... 2011; Peddibhotla 2013; Unique). This may also apply into adulthood with one 23 -year-old girl being short and slight (Risheg 2013). Others may be small as babies and toddlers but by four years old, for example, be of average weight for that age group (Al Kateb 2010). Two children were heavier and t ...
... 2011; Peddibhotla 2013; Unique). This may also apply into adulthood with one 23 -year-old girl being short and slight (Risheg 2013). Others may be small as babies and toddlers but by four years old, for example, be of average weight for that age group (Al Kateb 2010). Two children were heavier and t ...
Alu
... The highest Alu and gene densities – Chromosome 19, 22 Alu density is correlated in the order GC content > gene density > intron density The abundance of Alu subfamilies – Alu S > Alu J > Alu Y ...
... The highest Alu and gene densities – Chromosome 19, 22 Alu density is correlated in the order GC content > gene density > intron density The abundance of Alu subfamilies – Alu S > Alu J > Alu Y ...
Severe Combined Immunodeficiency (SCID)
... • SCID is a group of very rare-and potentially fatal-inherited disorders related to the immune system. • SCID makes those affected highly susceptible to life-threatening infections by viruses, bacteria and fungi. ...
... • SCID is a group of very rare-and potentially fatal-inherited disorders related to the immune system. • SCID makes those affected highly susceptible to life-threatening infections by viruses, bacteria and fungi. ...
Williams syndrome deficits in visual spatial Chromosome 7q11.23
... in 11 typical WS cases. Further analysis was performed using 1008H17 (containing the genes for FZD9 and FKBP6 genes) in 11 cases. The results indicated that BAC 1008H17 generated intermediate signals in 8 cases. Preliminary analyses on a subset of these were referred to in Kimura et al., 2000.34 The ...
... in 11 typical WS cases. Further analysis was performed using 1008H17 (containing the genes for FZD9 and FKBP6 genes) in 11 cases. The results indicated that BAC 1008H17 generated intermediate signals in 8 cases. Preliminary analyses on a subset of these were referred to in Kimura et al., 2000.34 The ...
Using Genetic Algorithms with Asexual
... mobile genetic units inside the genome, moving themselves to new locations or duplicating and inserting themselves elsewhere. These mobile units are called transposons [6], [16]. Transposons (also known as jumping genes) can be formed by one or several genes or just a control unit. The movement can ...
... mobile genetic units inside the genome, moving themselves to new locations or duplicating and inserting themselves elsewhere. These mobile units are called transposons [6], [16]. Transposons (also known as jumping genes) can be formed by one or several genes or just a control unit. The movement can ...
Chapter 10 (Conflict II)
... – Balancing selection • Reduced fertility/survival infected individuals • Sexual selection, avoiding infected individuals ...
... – Balancing selection • Reduced fertility/survival infected individuals • Sexual selection, avoiding infected individuals ...
Patterns of Segmental Duplication in the Human Genome
... frequency of duplication. First, we examined the relationship between the gene density and the duplicationenrichment index of a region. We used two gene databases for this analysis: known genes and Ensembl genes. Second, we examined the relationship between density of repetitive elements and extent ...
... frequency of duplication. First, we examined the relationship between the gene density and the duplicationenrichment index of a region. We used two gene databases for this analysis: known genes and Ensembl genes. Second, we examined the relationship between density of repetitive elements and extent ...
PINK
... sex-linked allele is never found on a Y chromosome sex-linked traits occur more often in men than women because women have 2 X chromosomes ( the second X usually carries the dominant allele and masks the recessive one) men experience sex-linked traits more often because they only have one X, which i ...
... sex-linked allele is never found on a Y chromosome sex-linked traits occur more often in men than women because women have 2 X chromosomes ( the second X usually carries the dominant allele and masks the recessive one) men experience sex-linked traits more often because they only have one X, which i ...
An assessment of chromosomal alterations detected by
... and structural chromosomal abnormalities by karyotypic ...
... and structural chromosomal abnormalities by karyotypic ...
On the mechanism of Wolbachia
... development aborts when sperm from an infected male fertilize an uninfected egg, due to the loss of improperly condensed paternal chromosomes (a notable exception is found in haplo-diploid arthropods species, where the loss of paternal chromosomes is not lethal but leads to haploid embryos that deve ...
... development aborts when sperm from an infected male fertilize an uninfected egg, due to the loss of improperly condensed paternal chromosomes (a notable exception is found in haplo-diploid arthropods species, where the loss of paternal chromosomes is not lethal but leads to haploid embryos that deve ...
Variation in the size of the oqhcontaining linear
... Species variation in the size of the ospA-containing plasmid The size of the ospA-containing linear DNA molecule, the largest of the plasmids in most isolates, was determined by constant-field electrophoresis in 0.2 YO agarose gels (a representative gel is shown in Fig. la), which have a linear rang ...
... Species variation in the size of the ospA-containing plasmid The size of the ospA-containing linear DNA molecule, the largest of the plasmids in most isolates, was determined by constant-field electrophoresis in 0.2 YO agarose gels (a representative gel is shown in Fig. la), which have a linear rang ...
Prospective diagnostic analysis of copy number variants using SNP
... Received 11 December 2012; revised 23 February 2013; accepted 28 March 2013 ...
... Received 11 December 2012; revised 23 February 2013; accepted 28 March 2013 ...
Dragon Investigations
... alleles—either the homozygous dominant (FF) or heterozygous (Ff) genotypes. You also know that Jill is a firebreathing female so she will have only one fire allele in her X chromosome. Since the other chromosome in her pair of sex chromosomes is a Y chromosome, her genotype for fire must be f– where ...
... alleles—either the homozygous dominant (FF) or heterozygous (Ff) genotypes. You also know that Jill is a firebreathing female so she will have only one fire allele in her X chromosome. Since the other chromosome in her pair of sex chromosomes is a Y chromosome, her genotype for fire must be f– where ...
Compressed q-gram Indexing for Highly Repetitive Biological
... are supported in O(log n) time per datum retrieved, are: L(a ∈ A, b ∈ B) returns the label associated to the pair (a, b) ∈ R or ⊥ if a is not related to b; R(a1 , a2 , b1 , b2 ) retrieves the set of elements (a, b) ∈ R such that a1 ≤ a ≤ a2 , b1 ≤ b ≤ b2 ; L(s) computes the set of pairs (a, b) relat ...
... are supported in O(log n) time per datum retrieved, are: L(a ∈ A, b ∈ B) returns the label associated to the pair (a, b) ∈ R or ⊥ if a is not related to b; R(a1 , a2 , b1 , b2 ) retrieves the set of elements (a, b) ∈ R such that a1 ≤ a ≤ a2 , b1 ≤ b ≤ b2 ; L(s) computes the set of pairs (a, b) relat ...
A Common Polygenic Basis for Quinine and
... genes not linked to Prp. Many genes near the QTL markers on chromosomes 3, 7, 8 and 9 have the potential to affect gustatory phenotypes (e.g. genes coding for ion channel proteins or neurotransmitter receptor proteins). However, confirmation of each QTL, and better position resolution for those conf ...
... genes not linked to Prp. Many genes near the QTL markers on chromosomes 3, 7, 8 and 9 have the potential to affect gustatory phenotypes (e.g. genes coding for ion channel proteins or neurotransmitter receptor proteins). However, confirmation of each QTL, and better position resolution for those conf ...
the contribution of gene movement to the two rules of speciation
... of developmental and reproductive biology of the X. We briefly introduce these mechanisms below, returning to the evidence for each in the next section. There are three mechanisms by which genes can move between chromosomes. The first involves the simple movement of a gene from one chromosome to ano ...
... of developmental and reproductive biology of the X. We briefly introduce these mechanisms below, returning to the evidence for each in the next section. There are three mechanisms by which genes can move between chromosomes. The first involves the simple movement of a gene from one chromosome to ano ...
December 2013 Newsletter - Wynnum Redlands Budgerigar Society
... wild type gene. They are mutations. This is regardless of whether they are dominant, sex linked or recessive. As already outlined, for a recessive characteristic to be manifest, the gene for it must be present on the appropriate site (locus) of each of the two homologous chromosomes. For example, fo ...
... wild type gene. They are mutations. This is regardless of whether they are dominant, sex linked or recessive. As already outlined, for a recessive characteristic to be manifest, the gene for it must be present on the appropriate site (locus) of each of the two homologous chromosomes. For example, fo ...
—1— User Guide © Copyright 2009 Robert C. Edgar, all rights
... The core components simulate inter- and intra-chromosome evolution, respectively. The inter-chromosome module (inter) simulates events involving two chromosomes, including chromosome fission, fusion and segmental moves and copies in which the target chromosome is different from the source chromosome ...
... The core components simulate inter- and intra-chromosome evolution, respectively. The inter-chromosome module (inter) simulates events involving two chromosomes, including chromosome fission, fusion and segmental moves and copies in which the target chromosome is different from the source chromosome ...
Chapter 9 Patterns of Inheritance Campbell Biology: Concepts & Connections,
... The all-purple F1 generation did not produce light purple flowers, as predicted by the blending hypothesis. Mendel needed to explain why – white color seemed to disappear in the F1 generation and ...
... The all-purple F1 generation did not produce light purple flowers, as predicted by the blending hypothesis. Mendel needed to explain why – white color seemed to disappear in the F1 generation and ...
Genetic analysis of genes on the 4th chromosome of
... either independently or synergistically, see Fig. 2 (Czerny et al., 1993). These two motifs are always found together except in the Pax6-like Drosophila protein Eye gone (Eyg), which lacks the amino-terminal PAI domain (Jun et al., 1998). In addition to their PD, Pax proteins often contain other con ...
... either independently or synergistically, see Fig. 2 (Czerny et al., 1993). These two motifs are always found together except in the Pax6-like Drosophila protein Eye gone (Eyg), which lacks the amino-terminal PAI domain (Jun et al., 1998). In addition to their PD, Pax proteins often contain other con ...