Evidence map›Paper›PMID 42642559›Full record

ArticleJournal of computer-aided molecular design2026

Examine neural network models for protein sequencing based features prediction.

Biswajit Senapati, Ranjita Das

Abstract read
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In one paragraph

Article in Journal of computer-aided molecular design, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Biswajit Senapati *Computer Science and Engineering, National Institute of Technology Mizoram, Chaltlang, Aizawl, Mizoram, 796012, India. biswajit.cse.phd@nitmz.ac.in.ORCID 0000-0002-9091-3414
Ranjita Das *Computer Science and Engineering, National Institute of Technology Agartala, Barjala, Agartala, Tripura, 799046, India.

Funding

DST and SERB, India EEQ/2020/000104
6 · The paper itself

Abstract

Protein functions are essential for understanding life at the molecular level. High-throughput sequencing generates vast amounts of raw protein sequences, but only about 1 percent have been carefully annotated with their functions. The experimental research needed to annotate these functions is costly and time-consuming, and lags behind the rapid growth in the number of sequences. This situation has led to the development of computational methods to predict protein functions. One proposed solution is an autoencoder framework that accurately predicts protein functions using both network and protein sequence data. Specifically, the framework encodes protein sequence information related to domains, families, and patterns-into a lengthy, sparse binary vector. The autoencoder has been rigorously tested both experimentally and statistically using two datasets. The results demonstrate that it outperforms other neural network models, including convolutional neural networks, recurrent neural networks, long short-term memory networks, and bidirectional long short-term memory networks. In comparison, the autoencoder achieved accuracy, precision, recall, and F1 scores of 0.94, 0.92, 0.92, and 0.92, respectively, on the protein meta- data and protein structure sequence datasets. The remainder of this study focuses on classifying feature types in protein sequence datasets.

Indexed as

Computational BiologyNeural Networks, ComputerProteinsSequence Analysis, ProteinAmino Acid SequenceAutoencoderConvolutional Neural NetworksDatabases, ProteinLong Short Term MemoryPrediction AlgorithmsRecurrent Neural NetworksProteinsBidirectional long short-term memory and autoencoderConvolutional neural networksLong short-term memoryRecurrent neural networks

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.