lncRNA-disease Predictor

SIMCLDA is used for lncRNA-disease prediction based on inductive matrix completion. For a new lncRNA, SIMCLDA calculates the interaction profile according to its sequence-similar neighbors and completes the association matrix using the primary feature vectors from the constructed feature matrices. Currently SIMCLDA only supports single lncRNA and only for human prediction. You have two ways to input data: directly input one lncRNA sequences or upload a .fasta file with fasta format.
Please input one lncRNA sequences (FASTA Format):

... or, upload a file: Browse ...

*Prediction of lncRNA-disease Associations Based on Inductive Matrix Completion. Bioinformatics. 2018. 34(19):3357-3364. Link to pubmed

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Contact wangdong79@smu.edu.cn or wangdong@ems.hrbmu.edu.cn
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