Analysis of Cross Sequence Similarities for Multiple - PolyU
... I-frame since the redundancy found between two consecutive frames is always significant when comparing with that found within the frame itself. In the field of DNA compression, current algorithms are analogous to intra-frame compression as redundant information is exploited only within one chromosom ...
... I-frame since the redundancy found between two consecutive frames is always significant when comparing with that found within the frame itself. In the field of DNA compression, current algorithms are analogous to intra-frame compression as redundant information is exploited only within one chromosom ...
View PDF - OMICS International
... errors, 45% zygotes appeared to be balanced following these sequential errors, representing a phenomenon of aneuploidy rescue [Table 3]. The fate of the embryos resulting from such balanced oocytes is not understood, but may lead to the formation of mosaic embryos, or to those with uniparental disom ...
... errors, 45% zygotes appeared to be balanced following these sequential errors, representing a phenomenon of aneuploidy rescue [Table 3]. The fate of the embryos resulting from such balanced oocytes is not understood, but may lead to the formation of mosaic embryos, or to those with uniparental disom ...
24 Recombination Hotspots in Nonallelic Homologous Recombination
... the HIV-resistant CCR5-Δ32 mutation (8). The apparent recent origin of this variant has lead to further work examining the possible role of the CCR5-Δ32 mutation in conferring resistance to recent plagues within the past 1000 years (9,10). This dating estimation is almost entirely predicated on an a ...
... the HIV-resistant CCR5-Δ32 mutation (8). The apparent recent origin of this variant has lead to further work examining the possible role of the CCR5-Δ32 mutation in conferring resistance to recent plagues within the past 1000 years (9,10). This dating estimation is almost entirely predicated on an a ...
Chromosome Variation
... only horse chromosomes from his mother. Additional reports of fertile female mules support the idea that their offspring inherit only horse chromosomes from their mother. When the father of a mule’s offspring is a horse, the offspring is horselike in appearance, because it apparently inherits horse ...
... only horse chromosomes from his mother. Additional reports of fertile female mules support the idea that their offspring inherit only horse chromosomes from their mother. When the father of a mule’s offspring is a horse, the offspring is horselike in appearance, because it apparently inherits horse ...
Cytogenetic Analysis Shows that the Unusually Large Chromosome
... We have discovered an inordinately large chromosome pair at the pachytene stage in the oocyte of the sex-limited p B (black larval marking) silkworm (Bombyx mori) strain (TWPB). We have analyzed the composition and arrangement of this large chromosome. A genetic linkage analysis shows that the large ...
... We have discovered an inordinately large chromosome pair at the pachytene stage in the oocyte of the sex-limited p B (black larval marking) silkworm (Bombyx mori) strain (TWPB). We have analyzed the composition and arrangement of this large chromosome. A genetic linkage analysis shows that the large ...
1q21 microdeletions
... molecular or DNA technology, in particular a technique using microarrays (array-CGH). This shows gains and losses of tiny amounts of DNA throughout the genome (also called duplications and deletions) and can show whether particular genes are present or not. A deletion so small that it can only be id ...
... molecular or DNA technology, in particular a technique using microarrays (array-CGH). This shows gains and losses of tiny amounts of DNA throughout the genome (also called duplications and deletions) and can show whether particular genes are present or not. A deletion so small that it can only be id ...
1q21 microdeletions
... and tongue thrusting. While three babies were breastfed, in one instance using techniques for babies with low muscle tone, others needed tube feeding and treatment for reflux, including a low-allergen milk formula. Two babies’ feeding difficulties were so severe that they were fed for a time by gast ...
... and tongue thrusting. While three babies were breastfed, in one instance using techniques for babies with low muscle tone, others needed tube feeding and treatment for reflux, including a low-allergen milk formula. Two babies’ feeding difficulties were so severe that they were fed for a time by gast ...
Imprinting of the Y Chromosome Influences Dosage Compensation
... dosage compensate normally regardless of the origin of their X chromosome. Imprinting therefore does not identify the X chromosome in male Drosophila. Both sex determination and dosage compensation in flies is determined by the number of X chromosomes present (Baker and Belote 1983). While the Y chr ...
... dosage compensate normally regardless of the origin of their X chromosome. Imprinting therefore does not identify the X chromosome in male Drosophila. Both sex determination and dosage compensation in flies is determined by the number of X chromosomes present (Baker and Belote 1983). While the Y chr ...
Supplemental Tables
... also posted at the AAA site, were also used in this analysis. The FlyBase inferred cytological map locations were assigned to all of the orthologs called in the four species. These associations were then ordered and sorted according to their scaffold assignments and molecular coordinates for each sp ...
... also posted at the AAA site, were also used in this analysis. The FlyBase inferred cytological map locations were assigned to all of the orthologs called in the four species. These associations were then ordered and sorted according to their scaffold assignments and molecular coordinates for each sp ...
CCMG Guidelines: Prenatal and Postnatal Diagnostic Testing for
... patients found to be homozygous for an autosomal recessive disease causing mutation and only one parent is a carrier for that mutation, assuming that other potential explanations such as non-paternity, heterozygous deletion, testing artifact, etc. have been excluded. Postnatal UPD testing should be ...
... patients found to be homozygous for an autosomal recessive disease causing mutation and only one parent is a carrier for that mutation, assuming that other potential explanations such as non-paternity, heterozygous deletion, testing artifact, etc. have been excluded. Postnatal UPD testing should be ...
X Chromosome Aneuploidy: A Look at the Effects of X Inactivation
... males and females are the same. The inactivation of one of the two X chromosomes appears to be random at the cellular level. Each cell inactivates one X chromosome randomly, independently of any other cell (Plath et al., 2002). At the organ and tissue level, certain genes may also undergo the proces ...
... males and females are the same. The inactivation of one of the two X chromosomes appears to be random at the cellular level. Each cell inactivates one X chromosome randomly, independently of any other cell (Plath et al., 2002). At the organ and tissue level, certain genes may also undergo the proces ...
Copy Number Analysis in Partek® Genomics Suite™ 6.6
... Figure 8: Viewing the Unpaired Copy Number dialog. Three kinds of baseline references are possible: using a baseline file distributed by Partek® (Option 1), using a previously created (cnmodel) reference file (Option 2), or using some or all of the samples in the current experiment as the reference ...
... Figure 8: Viewing the Unpaired Copy Number dialog. Three kinds of baseline references are possible: using a baseline file distributed by Partek® (Option 1), using a previously created (cnmodel) reference file (Option 2), or using some or all of the samples in the current experiment as the reference ...
The Deletion Stocks of Common Wheat
... of aberrations in the other chromosomes, for the difference in contraction of chro- tion stocks, we selected 156, 12, and 4 plants with one or more deletions and no that is, translocations and aneuploidy. mosomes between cells. The arm ratios of When two or more deletions occurred in the normal whea ...
... of aberrations in the other chromosomes, for the difference in contraction of chro- tion stocks, we selected 156, 12, and 4 plants with one or more deletions and no that is, translocations and aneuploidy. mosomes between cells. The arm ratios of When two or more deletions occurred in the normal whea ...
An Introduction to Genetic Analysis Chapter 18 Chromosome
... Triploids are usually autopolyploids. They arise spontaneously in nature or are constructed by geneticists from the cross of a 4x (tetraploid) and a 2x (diploid). The 2x and the x gametes unite to form a 3x triploid. Triploids are characteristically sterile. The problem, like that of monoploids, lie ...
... Triploids are usually autopolyploids. They arise spontaneously in nature or are constructed by geneticists from the cross of a 4x (tetraploid) and a 2x (diploid). The 2x and the x gametes unite to form a 3x triploid. Triploids are characteristically sterile. The problem, like that of monoploids, lie ...
KaryoNIM Postnatal EN
... Number of probes in the rest of the genome: 48000 probes Average detection capacity in the rest of the genome: 275 kb ...
... Number of probes in the rest of the genome: 48000 probes Average detection capacity in the rest of the genome: 275 kb ...
Large-Scale Chromosomal Changes
... ratio (the position of the centromere). Genetically, no viable crossover products are seen from recombination within the inversion when heterozygous, and as a result, flanking genes show a decrease in RF. d. Cytologically, reciprocal translocations may be detected by banding, or they may drastically ...
... ratio (the position of the centromere). Genetically, no viable crossover products are seen from recombination within the inversion when heterozygous, and as a result, flanking genes show a decrease in RF. d. Cytologically, reciprocal translocations may be detected by banding, or they may drastically ...
Comparative gene mapping in Arabidopsis lyrata chromosomes 6
... short arm also has a large heterochromatic knob with a large transposable element content, located in the region between the knob and the pericentromeric heterochromatin (Fransz et al., 2000 ; Arabidopsis Genome Initiative, 2000). Before one can compare genetic maps between two species, it is, howev ...
... short arm also has a large heterochromatic knob with a large transposable element content, located in the region between the knob and the pericentromeric heterochromatin (Fransz et al., 2000 ; Arabidopsis Genome Initiative, 2000). Before one can compare genetic maps between two species, it is, howev ...
Deep Insight Section
... chromosome pair or a chomosome segment derived from only one parent in a diploid individual. In fact, the information on this subject has grown so large that Pub Med, the webb-site of the US National Library of Medecine, by now lists over 550 original titles not to mention the so-call related articl ...
... chromosome pair or a chomosome segment derived from only one parent in a diploid individual. In fact, the information on this subject has grown so large that Pub Med, the webb-site of the US National Library of Medecine, by now lists over 550 original titles not to mention the so-call related articl ...
Unbalanced translocation, a major chromosome alteration
... from seven cell lines were used, because not only regions of LOH and site of copy number change but also numerical and structural alterations of chromosomes were able to be assessed in these cases, and because whole- and partial chromosome LOHs as well as partial chromosome LOHs with and without cop ...
... from seven cell lines were used, because not only regions of LOH and site of copy number change but also numerical and structural alterations of chromosomes were able to be assessed in these cases, and because whole- and partial chromosome LOHs as well as partial chromosome LOHs with and without cop ...
(NF1). - The Neuro Foundation
... are words that mean the same in this case. The area of the body affected may be just a small strip of skin or as big as a large “segment” of the body. Within these areas are the characteristic signs for NF1; outside them there are no signs at all. That area is unaffected by NF1. Usually the appearan ...
... are words that mean the same in this case. The area of the body affected may be just a small strip of skin or as big as a large “segment” of the body. Within these areas are the characteristic signs for NF1; outside them there are no signs at all. That area is unaffected by NF1. Usually the appearan ...
Segmental or mosaic NF1
... are words that mean the same in this case. The area of the body affected may be just a small strip of skin or as big as a large “segment” of the body. Within these areas are the characteristic signs for NF1; outside them there are no signs at all. That area is unaffected by NF1. Usually the appearan ...
... are words that mean the same in this case. The area of the body affected may be just a small strip of skin or as big as a large “segment” of the body. Within these areas are the characteristic signs for NF1; outside them there are no signs at all. That area is unaffected by NF1. Usually the appearan ...
A Novel Mouse Chromosome 17 Hybrid Sterility Locus
... The effects of heterospecific combinations of mouse chromosome 17 on male fertility and transmission ratio were investigated through a series of breeding studies. Animals were bred to carry complete chromosome 17 homologs, or portions thereof, from three differentsources-Mus domesticus, Mus spretus ...
... The effects of heterospecific combinations of mouse chromosome 17 on male fertility and transmission ratio were investigated through a series of breeding studies. Animals were bred to carry complete chromosome 17 homologs, or portions thereof, from three differentsources-Mus domesticus, Mus spretus ...
uncorrected page proofs
... more DNA it contains and usually the greater the number of genes that it carries. The members of each matching pair of chromosomes, such as the two number-5 chromosomes, are said to be homologous. Nonmatching chromosomes, such as a number-5 chromosome and a number-14 chromosome are said to be nonhom ...
... more DNA it contains and usually the greater the number of genes that it carries. The members of each matching pair of chromosomes, such as the two number-5 chromosomes, are said to be homologous. Nonmatching chromosomes, such as a number-5 chromosome and a number-14 chromosome are said to be nonhom ...
Correction to “Frequency of Undetected CYP2D6
... arrangement, we determined the percentage of heterozygous samples for each, which had a hybrid tandem. The “Any homozygous genotype” row included any sample with an initial homozygous genotype except those with duplications. Finally, the frequency of hybrid genes in samples originally genotyped as h ...
... arrangement, we determined the percentage of heterozygous samples for each, which had a hybrid tandem. The “Any homozygous genotype” row included any sample with an initial homozygous genotype except those with duplications. Finally, the frequency of hybrid genes in samples originally genotyped as h ...
14 Chromosomes
... • the position of the centromere, which appears as a constriction along the chromosome. In some cases, the centromere is near the middle (e.g. the number-2 chromosome in figure 14.6), while in others it is close to one end (e.g. the number-13 chromosome in figure 14.6). • patterns of light and dark ...
... • the position of the centromere, which appears as a constriction along the chromosome. In some cases, the centromere is near the middle (e.g. the number-2 chromosome in figure 14.6), while in others it is close to one end (e.g. the number-13 chromosome in figure 14.6). • patterns of light and dark ...