Searching journal content for articles similar to Issac and Raghava 14 (9): 1756.

Displaying results 1-10 of 6040
For checked items
  1. ...'Leary et al. 2016; Frankish et al. 2019; Salzberg 2019). The most widely used approaches to annotation are software pipelines such as MAKER, MAKER-P (Cantarel et al. 2008; Campbell et al. 2014), BRAKER, and BRAKER2 (Hoff et al. 2019; Brůna et al. 2021), which combine ab initio prediction, protein...
  2. ....2541 and 0.2503, respectively, surpassing the optimal result for GBLUP (0.2363) (Fig. 3B). Similar results were observed for AGG traits. CatBoost maintained the best predictive performance after applying the two SNP selection strategies (Fig. 3C). We applied the aforementioned strategy to the whole using...
  3. .... Genome-wide TE annotations are also improved, including larger unfragmented insertions. Moreover, MCHelper is an easy-to-install and easy-to-use tool.After two decades of sequencing projects, reference s for thousands of eukaryotic species are already available and many more are currently being sequenced...
  4. ...-RecCut uses contact maps predicted from ESM-2 (together with contextual embeddings of individual residues), taking advantage of its capability of generating contextual embeddings without using MSA so there are no time-consuming iterative searches of similar sequences. In addition, we developed...
  5. ...-learning model combining a CNN (one-hot encoded nucleotide bases as inputs) and a feedforward neural network (FNN; k-mer frequencies as inputs) (Fig. 1A,B). GutEuk uses a two-stage classification with user-defined confidence levels at each stage: The first stage differentiates between prokaryotic and eukaryotic...
  6. ...MarkS-T was performed on these assembled transcripts using the rounds of model parameter estimation and ab initio gene predictions (Tang et al. 2015).View larger version: In this window In a new window Figure 1. High-level diagram of the GeneMark-ETP processing of genomic, RNA-seq, and protein sequences. For more...
  7. ...interactions. 62 Deep learning can learn feature representations from transcriptomic data holds great 63 promise for predicting gene perturbations(Ahlmann-Eltze et al. 2025). Lotfollahi et al. 64 proposed scGen, a model that combines variational autoencoders with latent space 65 vector operations, which...
    ACCEPTED MANUSCRIPT
  8. ...for genomic data. Integrated into diverse architectures such as convoluted neural networks (CNNs), long short-term memory (LSTM), dilated CNNs, and transformers, ConvNeXt V2 blocks consistently improve performance, leading to similar prediction accuracy across these different model types. This reveals...
  9. ...of both species abundance and the similarity among the constitutive s.Experiments on complex eukaryotic sExperimental results on real data with varying ploidyAll the assemblers were tested on real HiFi reads for rice (homozygous diploid), potato (heterozygous diploid), and wax apple (autotetraploid...
  10. ..., USA; 6Departments of Biostatistics & Biomedical Engineering, UF Genetics Institute, University of Florida, Gainesville, Florida 32603, USA Corresponding authors: zengjy@westlake.edu.cn, mpsnyder@stanford.edu, sai.zhang@ufl.eduAbstractPolygenic risk score (PRS) is a widely used approach for predicting...
For checked items

Preprint Server