Maximum Likelihood Pedigree Reconstruction Using Integer Linear Programming

2012 ◽  
Vol 37 (1) ◽  
pp. 69-83 ◽  
Author(s):  
James Cussens ◽  
Mark Bartlett ◽  
Elinor M. Jones ◽  
Nuala A. Sheehan
10.29007/sghd ◽  
2018 ◽  
Author(s):  
James Cussens

Pedigrees are `family trees' relating groups of individuals which can usefully be seen as Bayesian networks. The problem of finding a maximum likelihood pedigree from genotypic data is encoded as an integer linear programming problem. Two methods of ensuring that pedigrees are acyclic are considered. Results on obtaining maximum likelihood pedigrees relating 20, 46 and 59 individuals are presented. Running times for larger pedigrees depend strongly on the data used but generally compare well with those in the literature. Solving is particularly fast when allele frequency is uniform.


2019 ◽  
Author(s):  
Vaibhav Rajan ◽  
Carl Kingsford ◽  
Xiuwei Zhang

AbstractMotivationThe study of the evolutionary history of biological networks enables deep functional understanding of various bio-molecular processes. Network growth models, such as the Duplication-Mutation with Complementarity (DMC) model, provide a principled approach to characterizing the evolution of protein-protein interactions (PPI) based on duplication and divergence. Current methods for model-based ancestral network reconstruction primarily use greedy heuristics and yield sub-optimal solutions.ResultsWe present a new Integer Linear Programming (ILP) solution for maximum likelihood reconstruction of ancestral PPI networks using the DMC model. We prove the correctness of our solution that is designed to find the optimal solution. It can also use efficient heuristics from general-purpose ILP solvers to obtain multiple optimal and near-optimal solutions that may be useful in many applications. Experiments on synthetic data show that our ILP obtains solutions with higher likelihood than those from previous methods, and is robust to noise and model mismatch. We evaluate our algorithm on two real PPI networks, with proteins from the families of bZIP transcription factors and the Commander complex. On both the networks, solutions from our ILP have higher likelihood and are in better agreement with independent biological evidence from other studies.AvailabilityA Python implementation is available at https://bitbucket.org/cdal/[email protected]


Author(s):  
Vaibhav Rajan ◽  
Ziqi Zhang ◽  
Carl Kingsford ◽  
Xiuwei Zhang

Abstract Motivation The study of the evolutionary history of biological networks enables deep functional understanding of various bio-molecular processes. Network growth models, such as the Duplication–Mutation with Complementarity (DMC) model, provide a principled approach to characterizing the evolution of protein–protein interactions (PPIs) based on duplication and divergence. Current methods for model-based ancestral network reconstruction primarily use greedy heuristics and yield sub-optimal solutions. Results We present a new Integer Linear Programming (ILP) solution for maximum likelihood reconstruction of ancestral PPI networks using the DMC model. We prove the correctness of our solution that is designed to find the optimal solution. It can also use efficient heuristics from general-purpose ILP solvers to obtain multiple optimal and near-optimal solutions that may be useful in many applications. Experiments on synthetic data show that our ILP obtains solutions with higher likelihood than those from previous methods, and is robust to noise and model mismatch. We evaluate our algorithm on two real PPI networks, with proteins from the families of bZIP transcription factors and the Commander complex. On both the networks, solutions from our ILP have higher likelihood and are in better agreement with independent biological evidence from other studies. Availability and implementation A Python implementation is available at https://bitbucket.org/cdal/network-reconstruction. Contact [email protected] Supplementary information Supplementary data are available at Bioinformatics online.


Sign in / Sign up

Export Citation Format

Share Document