Why model?

By O. Wolkenhauer. Frontiers in Physiology, 2013

665 citations recorded by the source corpus.

Next generation sequencing technologies are bringing about a renaissance of mining approaches. A comprehensive picture of the genetic landscape of an individual patient will be useful, for example, to identify groups of patients that do or do not respond to certain therapies. The high expectations may however not be satisfied if the number of patient groups with similar characteristics is going to be very large. I therefore doubt that mining sequence data will give us an understanding of why and when therapies work. For understanding the mechanisms underlying diseases, an alternative approach is to model small networks in quantitative mechanistic detail, to elucidate the role of gene and proteins in dynamically changing the functioning of cells. Here an obvious critique is that these models consider too few components, compared to what might be relevant for any particular cell function. I show here that mining approaches and dynamical systems theory are two ends of a spectrum of methodologies to choose from. Drawing upon personal experience in numerous interdisciplinary collaborations, I provide guidance on how to model by discussing the question “Why model?”

Subfields: Molecular Biology

View Paper: https://www.semanticscholar.org/paper/600a474dcb1e1dc4a58954923d1ee995110ccf41

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Molecular Biology

  1. Debashish Chowdhury
  2. L. Hardt
  3. Paul E. Smaldino
  4. Mehmet Karamanoglu
  5. Daniel W. O’Neill
  6. Andrea E. Martin
  7. Olivia Guest
  8. Eiko I. Fried

Citations in the corpus