125 results on '"Tsunoda, Tatsuhiko"'
Search Results
2. Advances in AI and machine learning for predictive medicine
3. PepCNN deep learning tool for predicting peptide binding residues in proteins using sequence, structural, and language model features
4. Time-dependent cell-state selection identifies transiently expressed genes regulating ILC2 activation
5. DeepInsight-3D architecture for anti-cancer drug response prediction with deep-learning on multi-omics
6. Splicing QTL analysis focusing on coding sequences reveals mechanisms for disease susceptibility loci
7. Utility of tissue-specific gene expression scores for gene prioritization in Mendelian diseases
8. Revisiting the definition of glioma recurrence based on a phylogenetic investigation of primary and re-emerging tumor samples: a case report
9. Analyses of non-coding somatic drivers in 2,658 cancer whole genomes
10. Association between high immune activity and worse prognosis in uveal melanoma and low-grade glioma in TCGA transcriptomic data
11. Landscape of prognostic signatures and immunogenomics of the AXL/GAS6 axis in renal cell carcinoma
12. Four pedigrees with aminoacyl-tRNA synthetase abnormalities
13. Profiling the inhibitory receptors LAG-3, TIM-3, and TIGIT in renal cell carcinoma reveals malignancy
14. Multiplexed single-cell pathology reveals the association of CD8 T-cell heterogeneity with prognostic outcomes in renal cell carcinoma
15. Structural basis of ethnic-specific variants of PAX4 associated with type 2 diabetes
16. Forecasting the spread of COVID-19 using LSTM network
17. SPECTRA: a tool for enhanced brain wave signal recognition
18. Homozygous ADCY5 mutation causes early-onset movement disorder with severe intellectual disability
19. A hypomorphic variant in EYS detected by genome-wide association study contributes toward retinitis pigmentosa
20. Effects of clovamide and its related compounds on the aggregations of amyloid polypeptides
21. Prognosis prediction model for conversion from mild cognitive impairment to Alzheimer’s disease created by integrative analysis of multi-omics data
22. Unveiling synapse pathology in spinal bulbar muscular atrophy by genome-wide transcriptome analysis of purified motor neurons derived from disease specific iPSCs
23. Bigram-PGK: phosphoglycerylation prediction using the technique of bigram probabilities of position specific scoring matrix
24. A comparison of machine learning classifiers for dementia with Lewy bodies using miRNA expression data
25. DeepInsight: A methodology to transform a non-image data to an image for convolution neural network architecture
26. Brain wave classification using long short-term memory network based OPTICAL predictor
27. Author Correction: A missense mutation in the HECT domain of NEDD4L identified in a girl with periventricular nodular heterotopia, polymicrogyria, and cleft palate
28. HseSUMO: Sumoylation site prediction using half-sphere exposures of amino acids residues
29. Risk prediction models for dementia constructed by supervised principal component analysis using miRNA expression data
30. Discovering MoRFs by trisecting intrinsically disordered protein sequence into terminals and middle regions
31. PhoglyStruct: Prediction of phosphoglycerylated lysine residues using structural properties of amino acids
32. Gene expression dataset for whole cochlea of Macaca fascicularis
33. Exploring predictive biomarkers from clinical genome-wide association studies via multidimensional hierarchical mixture models
34. Genome-wide association study suggests four variants influencing outcomes with ranibizumab therapy in exudative age-related macular degeneration
35. Publisher Correction: IMSindel: An accurate intermediate-size indel detection tool incorporating de novo assembly and gapped global-local alignment with split read analysis
36. Integrated analysis of human genetic association study and mouse transcriptome suggests LBH and SHF genes as novel susceptible genes for amyloid-β accumulation in Alzheimer’s disease
37. A novel homozygous missense mutation in the SH3-binding motif of STAMBP causing microcephaly-capillary malformation syndrome
38. A case report of reversible generalized seizures in a patient with Waardenburg syndrome associated with a novel nonsense mutation in the penultimate exon of SOX10
39. IMSindel: An accurate intermediate-size indel detection tool incorporating de novo assembly and gapped global-local alignment with split read analysis
40. Success: evolutionary and structural properties of amino acids prove effective for succinylation site prediction
41. An improved discriminative filter bank selection approach for motor imagery EEG signal classification using mutual information
42. 2D–EM clustering approach for high-dimensional data through folding feature vectors
43. Divisive hierarchical maximum likelihood clustering
44. Arete – candidate gene prioritization using biological network topology with additional evidence types
45. Siblings with optic neuropathy and RTN4IP1 mutation
46. Defects in autophagosome-lysosome fusion underlie Vici syndrome, a neurodevelopmental disorder with multisystem involvement
47. A novel missense mutation in the HECT domain of NEDD4L identified in a girl with periventricular nodular heterotopia, polymicrogyria and cleft palate
48. A combination of genetic and biochemical analyses for the diagnosis of PI3K-AKT-mTOR pathway-associated megalencephaly
49. Predicting MoRFs in protein sequences using HMM profiles
50. Gene masking - a technique to improve accuracy for cancer classification with high dimensionality in microarray data
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