Search Results
2. Molecular and genetic effect of coding variants in human
3. Transformer Models for Clinical Target Prediction using Pathology Report Text
4. Using heterogeneous, longitudinal EHR data for risk assessment and early detection of cardiovascular disease
5. Causal machine learning for reliable real-world evidence generation in healthcare
6. Generating Reliable and Responsive Observational Evidence: Reducing Pre-analysis Bias
7. Genetic and environmental determinants of recombination in coronaviruses
8. Genotype-Phenotype Correlation of T Cells from Aged and Alzheimer's Disease Subjects
9. Identifying and Targeting Master Regulators of Drug Resistance in Lung Adenocarcinoma through Network Analysis of Tumor Transcriptomic Data
10. Phenotyping with Partially Labeled, Partially Observed Data
11. Prediction of Human Gut Bacterial Secreted Proteins and their Interactions with Human Colonic Proteins
12. The itaconate-driven immunometabolic response to S. aureus promotes persistent lung infection
13. Using electronic health records to understand COVID-19 risks
14. Common and rare genetic effects on the transcriptome and their contribution to human traits
15. Mind the developmental gap: Identifying adverse drug effects across childhood to evaluate biological mechanisms from growth and development
16. Myeloid Heterogeneity in the Hippocampus
17. Systems-Level Approaches to Understanding Protein Synthesis
18. A Comparative Analysis of Genome Rearrangement in Ciliates
19. Characterizing molecular drivers of clinical outcome in pediatric acute leukemias by systems biology and machine learning
20. Genetic regulatory variant effects across tissues and individuals
21. Integration of Functional Genomic Data in Genetic Analysis
22. Mechanisms Underlying Phenotypic Heterogeneity in Simplex Autism Spectrum Disorders
23. Metabolic evaluation of genetic and environmental contributors to Alzheimer’s disease
24. Methods for modeling the dynamics of microbial communities
25. Post-transcriptional gene expression regulation in developmental disorders
26. Towards unified medical evidence computation from literature for evidence-based medicine
27. Computational Analysis of Biomolecular Data for Medical Applications from Bulk to Single-cell
28. Electronic Health Record-Derived Phenotyping Models to Improve Genomic Research in Stroke
29. Generative Models for Synthetic Biology
30. Loop Prediction and Homology Modeling with High Resolution
31. Mosaicism and the genetic architecture of congenital heart disease
32. Spatial and genomic analysis of the glioblastoma tumor microenvironment
33. The autophagosomal perspective: Tissue-specificity and cell-specificity of the autophagic response to starvation in vivo
34. Biological Insights from Geometry and Structure of Single-Cell Data
35. Computational Toxinology
36. Investigating and Supporting Sensemaking within Online Health Communities
37. Investigating the utility of exome sequencing for kidney disease
38. New Tools for Understanding and Engineering Complex Microbial Communities
39. Simulating drug responses in laboratory test time series with deep generative modeling
40. Systems Genetics of DNA Damage Tolerance – Cisplatin, RAD5 & CRISPR-mediated Nonsense
41. Adapting and Optimizing CBV-MRI and MEGAPRESS-MRS to Measure Slow Functional Changes in Normal and Abnormal Brains
42. Analysis of Oncogenic Signal Transduction with Application to KRAS Signaling Pathways
43. A Single-Cell Immune Map of Normal and Cancerous Breast Reveals an Expansion of Phenotypic States Driven by the Tumor Microenvironment
44. Attractor Metafeatures and Their Application in Biomolecular Data Analysis
45. Characterizing Immune Responses to Marburg Virus Infection in Animal Hosts Using Statistical Transcriptomic Analysis
46. Genomic and machine-learning analysis of germline variants in cancer
47. Leveraging patient-provided data to improve understanding of disease risk
48. Optimizing the Collection and Use of Patient-Generated Health Data
49. Quantitative Approaches to the Genomics of Clonal Evolution
50. Regulation of splicing networks in neurodevelopment
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