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1.
Brief Bioinform ; 25(2)2024 Jan 22.
Artículo en Inglés | MEDLINE | ID: mdl-38340092

RESUMEN

De novo peptide sequencing is a promising approach for novel peptide discovery, highlighting the performance improvements for the state-of-the-art models. The quality of mass spectra often varies due to unexpected missing of certain ions, presenting a significant challenge in de novo peptide sequencing. Here, we use a novel concept of complementary spectra to enhance ion information of the experimental spectrum and demonstrate it through conceptual and practical analyses. Afterward, we design suitable encoders to encode the experimental spectrum and the corresponding complementary spectrum and propose a de novo sequencing model $\pi$-HelixNovo based on the Transformer architecture. We first demonstrated that $\pi$-HelixNovo outperforms other state-of-the-art models using a series of comparative experiments. Then, we utilized $\pi$-HelixNovo to de novo gut metaproteome peptides for the first time. The results show $\pi$-HelixNovo increases the identification coverage and accuracy of gut metaproteome and enhances the taxonomic resolution of gut metaproteome. We finally trained a powerful $\pi$-HelixNovo utilizing a larger training dataset, and as expected, $\pi$-HelixNovo achieves unprecedented performance, even for peptide-spectrum matches with never-before-seen peptide sequences. We also use the powerful $\pi$-HelixNovo to identify antibody peptides and multi-enzyme cleavage peptides, and $\pi$-HelixNovo is highly robust in these applications. Our results demonstrate the effectivity of the complementary spectrum and take a significant step forward in de novo peptide sequencing.


Asunto(s)
Análisis de Secuencia de Proteína , Espectrometría de Masas en Tándem , Espectrometría de Masas en Tándem/métodos , Análisis de Secuencia de Proteína/métodos , Péptidos , Secuencia de Aminoácidos , Anticuerpos , Algoritmos
2.
Nucleic Acids Res ; 52(1): e3, 2024 Jan 11.
Artículo en Inglés | MEDLINE | ID: mdl-37941140

RESUMEN

Compared with proteins, DNA and RNA are more difficult languages to interpret because four-letter coded DNA/RNA sequences have less information content than 20-letter coded protein sequences. While BERT (Bidirectional Encoder Representations from Transformers)-like language models have been developed for RNA, they are ineffective at capturing the evolutionary information from homologous sequences because unlike proteins, RNA sequences are less conserved. Here, we have developed an unsupervised multiple sequence alignment-based RNA language model (RNA-MSM) by utilizing homologous sequences from an automatic pipeline, RNAcmap, as it can provide significantly more homologous sequences than manually annotated Rfam. We demonstrate that the resulting unsupervised, two-dimensional attention maps and one-dimensional embeddings from RNA-MSM contain structural information. In fact, they can be directly mapped with high accuracy to 2D base pairing probabilities and 1D solvent accessibilities, respectively. Further fine-tuning led to significantly improved performance on these two downstream tasks compared with existing state-of-the-art techniques including SPOT-RNA2 and RNAsnap2. By comparison, RNA-FM, a BERT-based RNA language model, performs worse than one-hot encoding with its embedding in base pair and solvent-accessible surface area prediction. We anticipate that the pre-trained RNA-MSM model can be fine-tuned on many other tasks related to RNA structure and function.


Asunto(s)
Aprendizaje Automático , ARN , Alineación de Secuencia , ADN/química , Proteínas , ARN/química , Solventes
3.
Front Mol Biosci ; 8: 614277, 2021.
Artículo en Inglés | MEDLINE | ID: mdl-34490342

RESUMEN

Capsule endoscopy is a leading diagnostic tool for small bowel lesions which faces certain challenges such as time-consuming interpretation and harsh optical environment inside the small intestine. Specialists unavoidably waste lots of time on searching for a high clearness degree image for accurate diagnostics. However, current clearness degree classification methods are based on either traditional attributes or an unexplainable deep neural network. In this paper, we propose a multi-task framework, called the multi-task classification and segmentation network (MTCSN), to achieve joint learning of clearness degree (CD) and tissue semantic segmentation (TSS) for the first time. In the MTCSN, the CD helps to generate better refined TSS, while TSS provides an explicable semantic map to better classify the CD. In addition, we present a new benchmark, named the Capsule-Endoscopy Crohn's Disease dataset, which introduces the challenges faced in the real world including motion blur, excreta occlusion, reflection, and various complex alimentary scenes that are widely acknowledged in endoscopy examination. Extensive experiments and ablation studies report the significant performance gains of the MTCSN over state-of-the-art methods.

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