Evaluation of deep-learning-based lncRNA identification tools
Yang, C.; Zhou, M.; Xie, H.; Zhu, H.
Show abstract
Long non-coding RNAs (lncRNAs, length above 200 nt) exert crucial biological roles and have been implicated in cancers1,2. To characterize newly discovered transcripts, one major issue is to distinguish lncRNAs from mRNAs. Since experimental methods are time-consuming and costly, computational methods are preferred for large-scale lncRNA identification. In a recent study, Amin et al.3 evaluated three deep-learning-based lncRNA identification tools (i.e., lncRNAnet4, LncADeep5, and lncFinder6) and concluded \"The LncADeep PR (precision recall) curve is just above the no-skill model and LncADeep showed poor overall performance\". This surprising conclusion is based on the authors use of a non-default setting of LncADeep. Actually, LncADeep has two models, one for full-length transcripts, and the other for transcripts including partial-length. Being aware of the difficulty of assembling full-length transcripts from RNA-seq dataset, LncADeeps default model is for transcripts including partial-length. However, according to the results posted on Amin et al.s website, the authors used LncADeep with full-length model, while they claimed to use the default setting of LncADeep, to identify lncRNAs from GENCODE dataset, which is composed of full- and partial-length transcripts. Thus, in their evaluation, the performance of LncADeep was underestimated. In this correspondence, we have tested LncADeeps default setting (i.e., model for transcripts including partial-length) on the datasets used in Amin et al.3, and LncADeep achieved overall the best performance compared with the other tools results reported by Amin et al.
Matching journals
The top 5 journals account for 50% of the predicted probability mass.
Similar papers in this journal
Similar papers in this journal
- DeepLncLoc: a deep learning framework for long non-coding RNA subcellular localization prediction based on subsequence embedding 95%
- CRISPR-DIPOFF: An Interpretable Deep LearningApproach for CRISPR Cas-9 Off-Target Prediction 94%
- LDBlockShow: a fast and convenient tool for visualizing linkage disequilibrium and haplotype blocks based on variant call format files 93%
Similar papers in this journal
Similar papers in this journal
- GenoM7GNet: An Efficient N7-methylguanosine Site Prediction Approach Based on a Nucleotide Language Model 95%
- Stratified Test Accurately Identifies Differentially Expressed Genes Under Batch Effects in Single-Cell Data 93%
- miRCoop: Identifying Cooperating miRNAs via Kernel Based Interaction Tests 93%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.