Genetic association and gene–gene interaction analyses suggest likely involvement of ITGB3 and TPH2 with autism spectrum disorder (ASD) in the Indian population

Author(s):  
Asem Surindro Singh ◽  
Rashmi Chandra ◽  
Subhrangshu Guhathakurta ◽  
Swagata Sinha ◽  
Anindita Chatterjee ◽  
...  
Author(s):  
Deepak Verma ◽  
Barnali Chakraborti ◽  
Arijit Karmakar ◽  
Tirthankar Bandyopadhyay ◽  
Asem Surindro Singh ◽  
...  

IUBMB Life ◽  
2018 ◽  
Vol 70 (8) ◽  
pp. 763-776 ◽  
Author(s):  
Ye Bai ◽  
Shuang Qiu ◽  
Yan Li ◽  
Yong Li ◽  
Weijing Zhong ◽  
...  

2018 ◽  
Author(s):  
Utku Norman ◽  
A. Ercument Cicek

AbstractWhole exome sequencing (WES) studies for Autism Spectrum Disorder (ASD) could identify only around six dozen risk genes to date because the genetic architecture of the disorder is highly complex. To speed the gene discovery process up, a few network-based ASD gene discovery algorithms were proposed. Although these methods use static gene interaction networks, functional clustering of genes is bound to evolve during neurodevelopment and disruptions are likely to have a cascading effect on the future associations. Thus, approaches that disregard the dynamic nature of neurodevelopment are limited in power. Here, we present a spatio-temporal gene discovery algorithm for ASD, which leverages information from evolving gene coexpression networks of neurodevelopment. The algorithm solves a variant of prize-collecting Steiner forest-based problem on coexpression networks to model neurodevelopment and transfer information from precursor neurodevelopmental windows. The decisions made by the algorithm can be traced back, adding interpretability to the results. We apply the algorithm on WES data of 3,871 samples and identify risk clusters using BrainSpan coexpression networks of earlyand mid-fetal periods. On an independent dataset, we show that incorporation of the temporal dimension increases the prediction power: Predicted clusters are hit more and show higher enrichment in ASD-related functions compared to the state-of-the-art. Code is available at http://ciceklab.cs.bilkent.edu.tr/ST-Steiner/.


2008 ◽  
Vol 441 (1) ◽  
pp. 56-60 ◽  
Author(s):  
Shruti Dutta ◽  
Swagata Sinha ◽  
Saurabh Ghosh ◽  
Anindita Chatterjee ◽  
Shabina Ahmed ◽  
...  

2020 ◽  
Author(s):  
Margot Gunning ◽  
Paul Pavlidis

AbstractDiscovering genes involved in complex human genetic disorders is a major challenge. Many have suggested that machine learning (ML) algorithms using gene networks can be used to supplement traditional genetic association-based approaches to predict or prioritize disease genes. However, questions have been raised about the utility of ML methods for this type of task due to biases within the data, and poor real-world performance. Using autism spectrum disorder (ASD) as a test case, we sought to investigate the question: Can machine learning aid in the discovery of disease genes? We collected thirteen published ASD gene prioritization studies and evaluated their performance using known and novel high-confidence ASD genes. We also investigated their biases towards generic gene annotations, like number of association publications. We found that ML methods which do not incorporate genetics information have limited utility for prioritization of ASD risk genes. These studies perform at a comparable level to generic measures of likelihood for the involvement of genes in any condition, and do not out-perform genetic association studies. Future efforts to discover disease genes should be focused on developing and validating statistical models for genetic association, specifically for association between rare variants and disease, rather than developing complex machine learning methods using complex heterogeneous biological data with unknown reliability.


2021 ◽  
pp. 100024
Author(s):  
Vellingiri Balachandar ◽  
Geetha Bharathi ◽  
Kaavya Jayaramayya ◽  
Anila Venugopal ◽  
Iyer Mahalaxmi ◽  
...  

Author(s):  
D.Mandamkulathil . ◽  
AA.Pillai . ◽  
SA.Poovathinal . ◽  
SK.Chengappa . ◽  
A.Chandrasekar . ◽  
...  

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