Subscribe to the gold package and get unlimited access to Shamra Academy
Register a new userA simple unified explanation of several genetic issues on todays human population and on archaic humans
56
0
0.0
(
0
)
Added by
Juan Seoane-Sepulveda
Publication date
2017
fields
Biology
and research's language is
English
Ask ChatGPT about the research
No Arabic abstract
We will give a simple, unified, possible explanation of several debated genetic issues on todays humans, Neandertals and Denisovans. In particular it is shown by means of a simple mathematical model why there is little genetic variation in todayss human population or in Western Neandertal population, why all mtDNA and y-chromosomes in todays humans seem to have African origin with no trace of Neandertal nor Denosovan mtDNA or y-chromosomes, why a big part of the European gene pool is young (from Neolitic time), and why todays East Asians have mode Neandertal genes than todays Europeans.
rate research
Read More
Computer simulations of the Penna ageing model suggest that already a small fraction of births with enhanced number of new mutations can negatively influence the whole population.
We propose a mathematical model to analyze the time evolution of the total number of infected population with Covid-19 disease at a region in the ongoing pandemic. Using the available data of Covid-19 infected population on various countries we formulate a model which can successfully track the time evolution from early days to the saturation period in a given wave of this infectious disease. It involves a set of effective parameters which can be extracted from the available data. Using those parameters the future trajectories of the disease spread can also be projected. A set of differential equations is also proposed whose solutions are these time evolution trajectories. Using such a formalism we project the future time evolution trajectories of infection spread for a number of countries where the Covid-19 infection is still rapidly rising.
Coalescent theory combined with statistical modeling allows us to estimate effective population size fluctuations from molecular sequences of individuals sampled from a population of interest. When sequences are sampled serially through time and the distribution of the sampling times depends on the effective population size, explicit statistical modeling of sampling times improves population size estimation. Previous work assumed that the genealogy relating sampled sequences is known and modeled sampling times as an inhomogeneous Poisson process with log-intensity equal to a linear function of the log-transformed effective population size. We improve this approach in two ways. First, we extend the method to allow for joint Bayesian estimation of the genealogy, effective population size trajectory, and other model parameters. Next, we improve the sampling time model by incorporating additional sources of information in the form of time-varying covariates. We validate our new modeling framework using a simulation study and apply our new methodology to analyses of population dynamics of seasonal influenza and to the recent Ebola virus outbreak in West Africa.
There is an urgent and well-recognized need to extend genetic studies to diverse populations, but several obstacles continue to be prohibitive, including (but not limited to) the difficulty of recruiting individuals from diverse populations in large numbers and the lack of representation in available genomic references. These obstacles notwithstanding, studying multiple diverse populations would provide informative, population-specific insights. Using Native Hawaiians as an example of an understudied population with a unique evolutionary history, I will argue that by developing key genomic resources and integrating evolutionary thinking into genetic epidemiology, we will have the opportunity to efficiently advance our knowledge of the genetic risk factors, ameliorate health disparity, and improve healthcare in this underserved population.
Spatial patterning can be crucially important for understanding the behavior of interacting populations. Here we investigate a simple model of parasite and host populations in which parasites are random walkers that must come into contact with a host in order to reproduce. We focus on the spatial arrangement of parasites around a single host, and we derive using analytics and numerical simulations the necessary conditions placed on the parasite fecundity and lifetime for the populations long-term survival. We also show that the parasite population can be pushed to extinction by a large drift velocity, but, counterintuitively, a small drift velocity generally increases the parasite population.
Log in to be able to interact and post comments
comments
Fetching comments
Sign in to be able to follow your search criteria
