Article Type : Research Article
Authors : Ubani SI
Keywords : Genotype; Phenotype; Vectors; Atypical; Sequence; Traits; Species
Genotype
vectors trasmodification had recently been known to be a typical. The host
plant retains the traits of the source plant in the second hereditary level.
This however did not retain the third, fourth etc. resultant phenotype
sequence. The research method involved the ascertainment of the minimum gene
sequence. For the transmodification of the base phenotype sequence. The results
was an amalgamation of traits. The gene sequence appeared similar and contained
useful features of the source plant. There was however new species traits of
the atypical level. The effect was a resilient species to pathogen vectors and
microbial effects in the environment. The minimum number of gene sequence was
205 to produce 33% change in the traits. Less than this 56 had only a 7% trait
conversion and could not be used in treatment of species of pathogens effects.
The transmodification was the degree of vector
application of genetic matter of the meniscus. The effect was an invasion of
the cellular membrane. The alteration of the permeability and protoplasma
density and size. Research in the literature had documented several aspects of
gentotype modification. But there lacks sufficient literature on phenotype
traits. The differences between genotypical and phenotypical traits was the
protoplasma. Most unicellular and multicellular organism contained genotypes.
But the phenotype was only found in prokaryotes. These were essentially
multicellular and not in eukaryotes known as unicellular. Most non-budded
plants were known as unicellular. The proteome was the same and led to low
growth diversity in (Figure 1). Prokaryotes
had 22% additional proteome. This was found with the protoplasm. Under a
microscope it appears shaded and different from the cell membrane of the
species. Showed species of multicellular (Figure 2). Atypical
transmodification led to two different applications absorption and adsorption
of the genetic matter. Absorption was preferred as the genetic matter sequences
was high. This was important in virology for the resistance to strains of
pathogens. More resilient pathologies could be developed by the application of
genetic matter from two different regions of prokaryotic species.
Four different species of eukaryotes and prokaryotes were obtained from Figure 1 and Figure 2..
(a) (b) (c) (d)
Figure 1: Eukaryotes with absence of proteome for (a) Acorus (b) Aesculus (c) Triloba and (d) Athyrium.
(a) (b) (c) (d)
Figure 2: Prokaryotes showed presence of proteome in cells for (a) Laxum (b) Pavia (c) Gerardii and (d) Rubrum
Figure 3: Effect of the time on the transmodification of the membrane.
Figure 4: Protoplasma density of the sequence of specimens and atypical samples.
These plants were then condensed and converted to
genetic matter. Then invasively added to each class of species. Figure 1 and
figure 2 were used to apply to the eukaryotes and prokaryotes interchangeably.
This was to determine the effect of cellularity on hereditary of eukaryotic and
phenotypic conversion. The cultures were kept over time and changes were
studied for each species. In each instance for 1 hour, 3 hours and 6 hours.
This was to replicate the adsorption, transmodification and absorption of the
genetically extracted matter (Figure 3). The effect was categorized into
different hereditary levels. When the gene sequence was below 50% there no
genotype changes at 50% hereditary change to two levels of species and above
50% phenotypic species of level 3 and level 4.
The minimum gene sequence of transmodification was set
from the average of the specimens. This was because external factors of the
environment could contribute to discrepancies in the hierarchy determination of
phenotypic virology in (Table 1). Table
1 was obtained from gene sequence extraction from the protoplasm of each
plants. The atypical specimens for transferred genetic matter were Acorus and
Laxum. These had the base genotypes and phenotype sequences for each. The
protoplasma density was derived from the gene sequence experiment for the
sequence of specimens. To ascertain the time for each hierarchial transmodification.
This was classified into three subcategories of 1hr, 3 hrs and 6hrs for the
studies. Illustrated sample 1, 2,
3 were unaffected by the addition of the genetic matter A1. Whereas samples 4,
5 had third and second level hierarchal phenotypical change of the proteome
(Figure 4). The study did not results in
fourth sequence of traits of the genes.The gene sequences of the genotype and
phenotype atypical specimens were used for discrepancies. This was to determine
the strand contribution to the hierarchy of the genes. Showed
T strand had the most contribution to the density of the protoplasma. Therefore
was inhibitor of viral effects (Table 2). The G strand had the least effect on
the species of the genotype. Showed
the G strand produced inhibition and contributed the most to hierarchial level
of the species of the gene specimen (Table 3) [1-5].
Gene sequence studies
showed the transmodification had an effect on the traits. Each sample had its
gene sequences. The atypical specimens with prokaryotic traits resulted in
third and second level hierarchies in the proteomes of the plants. This could
be used in development of pathologically resistant species of viral effects.
The research improved the literature in the field of virology and pathologically
development of strains of the plants.