ArticleMolecules (Basel, Switzerland)2018
Integrating Multiple Interaction Networks for Gene Function Inference.
Article in Molecules (Basel, Switzerland), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
3 citing papers in PubMed.
- Investigation of sex expression profiles and the cantharidin biosynthesis genes in two blister beetles.PloS one · 2023Article
- Predicting effective drug combinations using gradient tree boosting based on features extracted from drug-protein heterogeneous network.BMC bioinformatics · 2019Article
- Molecular Computing and Bioinformatics.Molecules (Basel, Switzerland) · 2019Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
Abstract
In the past few decades, the number and variety of genomic and proteomic data available have increased dramatically. Molecular or functional interaction networks are usually constructed according to high-throughput data and the topological structure of these interaction networks provide a wealth of information for inferring the function of genes or proteins. It is a widely used way to mine functional information of genes or proteins by analyzing the association networks. However, it remains still an urgent but unresolved challenge how to combine multiple heterogeneous networks to achieve more accurate predictions. In this paper, we present a method named ReprsentConcat to improve function inference by integrating multiple interaction networks. The low-dimensional representation of each node in each network is extracted, then these representations from multiple networks are concatenated and fed to gcForest, which augment feature vectors by cascading and automatically determines the number of cascade levels. We experimentally compare ReprsentConcat with a state-of-the-art method, showing that it achieves competitive results on the datasets of yeast and human. Moreover, it is robust to the hyperparameters including the number of dimensions.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.