DAVI: Deep learning-based tool for alignment and single nucleotide variant identification

G Gupta, S Saini - Machine Learning: Science and Technology, 2020 - iopscience.iop.org
Next-generation sequencing (NGS) technologies have provided affordable but errorful ways
to generate raw genetic data. To extract variant information from billions of NGS reads is still …

[引用][C] DEEP LEARNING FRAMEWORK FOR EFFICIENT PREDICTION OF CAUSATIVE MUTATIONS, GENES AND THEIR SUSCEPTIBILITY TO AUTISM SPECTRUM …

V PreamSudha, MS Vijaya - 2009