bioRxiv Science⌕ Search

Biology subjects

Hanson, E. A.

Publications and source records attributed to Hanson, E. A..

2 recordsLinked to original sources

Perfusion estimation using MRI-based measurements and a porous media flow model

The measurement of perfusion and filtration of blood in biological tissue give rise to important clinical parameters used in diagnosis, follow-up, and therapy. In this paper we address techniques for perfusion analysis using processed contrast agent concentration data from dynamic MRI acquisitions. New methodology for analysis is evaluated and verified using synthetic data generated on a tissue geometry. Author summaryAccurate knowledge of tissue perfusion is crucial for proper diagnostics and treatment of several medical disorders. Traditional methods based on medical imaging are fast, but usually lack precision and robustness. In this paper, we address methodology to develop better diagnosis and treatment strategies for malignant tumors and stroke where blood perfusion may be altered. In our work, mathematical models for estimating perfusion are calibrated using magnetic resonance imaging (MRI) data, and more accurate representations of tissue parameters are provided. This methodology is a step towards minimal invasive and individually tailored diagnosis and treatment. We demonstrate the methodology with a twin-experiment using models of different complexity for generating data and estimating the tissue parameters. Both models are based on a mathematical description of how fluids flows in a porous medium, where the data-generating model uses higher resolution and a network representation of blood vessels than the estimating model. The calibration of unknown tissue parameters is done using a statistical framework, and the choice of methodology is motivated by applications from sub-surface reservoir characterization.

systems biology↗

Mutations in coral soma and sperm imply lifelong stem cell differentiation

In many animals, the germline differentiates early in embryogenesis, so only mutations that accumulate in germ cells are inherited by offspring1. Exceptions to this developmental process may indicate that other mechanisms have evolved to limit the effects of deleterious mutation accumulation2. Stony corals are animals that can live for hundreds of years3 and have long been thought to produce gametes from somatic tissue4. To clarify conflicting evidence about germline-soma distinction in corals, we sequenced high coverage, full genomes with technical replicates for parent coral branches and their sperm pools. We identified post-embryonic single nucleotide variants (SNVs) unique to each parent branch, then checked if each SNV was shared by the respective sperm pool: 26% of post-embryonic SNVs were shared by the sperm but 74% were not. We also identified germline SNVs, those that were present in the sperm but not in the parent. These data suggest that self-renewing stem cells in corals differentiate into germ and soma throughout the adult life of the colony, with SNV rates and patterns differing markedly in stem, soma, and germ lineages. In addition to informing the important place in the evolutionary spectrum from non-Weismannian to Weismmanian animals that corals occupy, these insights inform how corals may generate adaptive diversity necessary in the face of global climate change.

genetics↗