Evidence map›Paper›PMID 30320286›Full record

ArticleACS omega2018

Prediction of Compound Profiling Matrices, Part II: Relative Performance of Multitask Deep Learning and Random Forest Classification on the Basis of Varying Amounts of Training Data.

Raquel Rodríguez-Pérez, Jürgen Bajorath

Abstract read
In one paragraph

Article in ACS omega, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Recent Advances in In Silico Target Fishing.Molecules (Basel, Switzerland) · 2021
    Review
  6. Article
  7. Article
  8. Article
  9. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Raquel Rodríguez-PérezDepartment of Life Science Informatics, B-IT, LIMES Program Unit Chemical Biology and Medicinal Chemistry, Rheinische Friedrich-Wilhelms-Universität, Endenicher Allee 19c, D-53115 Bonn, Germany.
Jürgen BajorathDepartment of Life Science Informatics, B-IT, LIMES Program Unit Chemical Biology and Medicinal Chemistry, Rheinische Friedrich-Wilhelms-Universität, Endenicher Allee 19c, D-53115 Bonn, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Currently, there is a high level of interest in deep learning and multitask learning in many scientific fields including the life sciences and chemistry. Herein, we investigate the performance of multitask deep neural networks (MT-DNNs) compared to random forest (RF) classification, a standard method in machine learning, in predicting compound profiling experiments. Predictions were carried out on a large profiling matrix extracted from biological screening data. For model building, submatrices with varying data density of 5-100% were generated to investigate the influence of data sparseness on prediction performance. MT-DNN models were directly compared to RF models, and control calculations were also carried out using single-task DNNs (ST-DNNs). On the basis of compound recall, the performance of ST-DNN was consistently lower than that of the other methods. Compared to RF, MT-DNN models only yielded better prediction performance for individual assays in the profiling matrix when training data were very sparse. However, when the matrix density increased to at least 25-45%, per-assay RF models met or partly exceeded the prediction performance of MT-DNN models. When the average performances of RF and MT-DNN over the grid of all targets were compared, MT-DNN was slightly superior to RF, which was a likely consequence of multitask learning. Overall, there was no consistent advantage of MT-DNN over standard RF classification in predicting the results of compound profiling assays under varying conditions. In the presence of very sparse training data, prediction performance was limited. Under these challenging conditions, MT-DNN was the preferred approach. When more training data became available and prediction performance increased, RF performance was not inferior to MT-DNN.

Identifiers

PMID30320286
PMCPMC6175492

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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.