All Stories

  1. Genetic demultiplexing of pooled single-cell RNA-sequencing samples in cancer facilitates effective experimental design
  2. Correcting for experiment-specific variability in expression compendia can remove underlying signals
  3. Expanding and Remixing the Metadata Landscape
  4. Transparency and reproducibility in artificial intelligence
  5. Responsible, practical genomic data sharing that accelerates research
  6. Incorporating biological structure into machine learning models in biomedicine
  7. Recommendations to enhance rigor and reproducibility in biomedical research
  8. Compressing gene expression data using multiple latent space dimensionalities learns complementary biological representations
  9. Correcting for experiment-specific variability in expression compendia can remove underlying signals
  10. Analysis of ISCB honorees and keynotes reveals disparities
  11. Integrative Analysis Identifies Candidate Tumor Microenvironment and Intracellular Signaling Pathways that Define Tumor Heterogeneity in NF1
  12. Pseudomonas aeruginosa lasR mutant fitness in microoxia is supported by an Anr-regulated oxygen-binding hemerythrin
  13. Graph biased feature selection of genes is better than random for many genes
  14. Integrative analysis identifies candidate tumor microenvironment and intracellular signaling pathways that define tumor heterogeneity in NF1
  15. Integrated phosphoproteomics and transcriptional classifiers reveal hidden RAS signaling dynamics in multiple myeloma
  16. Pseudomonas aeruginosa lasR mutant fitness in microoxia is supported by an Anr-regulated oxygen-binding hemerythrin
  17. Reusing label functions to extract multiple types of biomedical relationships from biomedical abstracts at scale
  18. Open collaborative writing with Manubot
  19. Sequential compression across latent space dimensions enhances gene expression signatures
  20. Integrated Phosphoproteomics and Transcriptional Classifiers Reveal Hidden RAS Signaling Dynamics in Multiple Myeloma
  21. Bayesian deep learning for single-cell analysis
  22. New Drosophila Long-Term Memory Genes Revealed by Assessing Computational Function Prediction Methods
  23. A Parasite's Perspective on Data Sharing
  24. Learning and Imputation for Mass-spec Bias Reduction (LIMBR)
  25. Discovering pathway and cell-type signatures in transcriptomic compendia with machine learning
  26. Discovering pathway and cell-type signatures in transcriptomic compendia with machine learning
  27. New Drosophila long-term memory genes revealed by assessing computational function prediction methods.
  28. MultiPLIER: a transfer learning framework reveals systemic features of rare autoimmune disease
  29. Parameter tuning is a key part of dimensionality reduction via deep variational autoencoders for single cell RNA transcriptomics
  30. Specific histone modifications associate with alternative exon selection during mammalian development
  31. PathCORE-T: identifying and visualizing globally co-occurring pathways in large transcriptomic compendia
  32. Learning and Imputation for Mass-spec Bias Reduction (LIMBR)
  33. Machine Learning Detects Pan-cancer Ras Pathway Activation in The Cancer Genome Atlas
  34. Oncogenic Signaling Pathways in The Cancer Genome Atlas
  35. Research: Sci-Hub provides access to nearly all scholarly literature
  36. Sci-Hub provides access to nearly all scholarly literature
  37. A Multimodal Strategy Used by a Large c-di-GMP Network
  38. A Pilot Characterization of the Human Chronobiome
  39. ADAGE signature analysis: differential expression analysis with data-defined gene sets
  40. Sci-Hub provides access to nearly all scholarly literature
  41. Sci-Hub provides access to nearly all scholarly literature
  42. Enter the matrix: Interpreting unsupervised feature learning with matrix decomposition to discover hidden knowledge in high-throughput omics data
  43. Machine Learning Analysis Identifies Drosophila Grunge/Atrophin as an Important Learning and Memory Gene Required for Memory Retention and Social Learning
  44. Extracting a Biologically Relevant Latent Space from Cancer Transcriptomes with Variational Autoencoders
  45. Implicating candidate genes at GWAS signals by leveraging topologically associating domains
  46. Functional network community detection can disaggregate and filter multiple underlying pathways in enrichment analyses
  47. Sci-Hub provides access to nearly all scholarly literature
  48. Tissue-specific network-based genome wide study of amygdala imaging phenotypes to identify functional interaction modules
  49. Privacy-preserving generative deep neural networks support clinical data sharing
  50. Unsupervised Extraction of Stable Expression Signatures from Public Compendia with an Ensemble of Neural Networks
  51. Machine learning analysis identifies Drosophila Grunge/Atrophin as an important learning and memory gene required for memory retention and social learning.
  52. ADAGE signature analysis: differential expression analysis with data-defined gene sets
  53. PathCORE: Visualizing globally co-occurring pathways in large transcriptomic compendia
  54. Data-Sharing Models
  55. Opportunities And Obstacles For Deep Learning In Biology And Medicine
  56. Celebrating parasites
  57. A novel multi-network approach reveals tissue-specific cellular modulators of fibrosis in systemic sclerosis
  58. Cross-Platform Normalization Enables Machine Learning Model Training On Microarray And RNA-Seq Data Simultaneously
  59. Reproducibility of computational workflows is automated using continuous analysis
  60. Tell me your neighbors, and I will tell you what you are
  61. A machine learning classifier trained on cancer transcriptomes detects NF1 inactivation signal in glioblastoma
  62. Cheap-seq
  63. Semi-supervised learning of the electronic health record for phenotype stratification
  64. Implicating candidate genes at GWAS signals by leveraging topologically associating domains
  65. How to know what we dont
  66. Comprehensive Cross-Population Analysis of High-Grade Serous Ovarian Cancer Supports No More Than Three Subtypes
  67. System-wide automatic extraction of functional signatures in Pseudomonas aeruginosa with eADAGE
  68. A stromal focus reveals tumor immune signatures
  69. A machine learning classifier trained on cancer transcriptomes detects NF1 inactivation signal in glioblastoma
  70. An expanded evaluation of protein function prediction methods shows an improvement in accuracy
  71. Gut check
  72. Integrative networks illuminate biological factors underlying gene-disease associations
  73. The future is unsupervised
  74. Pathway and network-based strategies to translate genetic discoveries into effective therapies
  75. Evolution of High Cellulolytic Activity in Symbiotic Streptomyces through Selection of Expanded Gene Content and Coordinated Gene Expression
  76. Reproducible Computational Workflows with Continuous Analysis
  77. Tribe: The collaborative platform for reproducible web-based analysis of gene sets
  78. Nothing but a hound dog
  79. Pathway and network-based strategies to translate genetic discoveries into effective therapies
  80. CoINcIDE: All together now
  81. Genetic Association–Guided Analysis of Gene Networks for the Study of Complex Traits
  82. Genomic characterization of patient-derived xenograft models established from fine needle aspirate biopsies of a primary pancreatic ductal adenocarcinoma and from patient-matched metastatic sites
  83. Semi-Supervised Learning of the Electronic Health Record with Denoising Autoencoders for Phenotype Stratification
  84. A Novel Multi-network Approach Reveals Tissue-specific Cellular Modulators of Fibrosis in Systemic Sclerosis, Pulmonary Fibrosis and Pulmonary Arterial Hypertension
  85. Erratum to: Evolving hard problems: generating human genetics datasets with a complex etiology
  86. Cross-platform normalization of microarray and RNA-seq data for machine learning applications
  87. Network-based analysis of genetic variants associated with hippocampal volume in Alzheimer’s disease: a study of ADNI cohorts
  88. ADAGE-Based Integration of Publicly Available Pseudomonas aeruginosa Gene Expression Data with Denoising Autoencoders Illuminates Microbe-Host Interactions
  89. Leveraging global gene expression patterns to predict expression of unmeasured genes
  90. ADAGE analysis of publicly available gene expression data collections illuminates Pseudomonas aeruginosa-host interactions
  91. Comprehensive cross-population analysis of high-grade serous ovarian cancer supports no more than three subtypes
  92. Cross-platform normalization of microarray and RNA-seq data for machine learning applications
  93. Cross-platform normalization of microarray and RNA-seq data for machine learning applications
  94. Identification of shared and unique susceptibility pathways among cancers of the lung, breast, and prostate from genome-wide association studies and tissue-specific protein interactions
  95. Recent Advances and Emerging Applications in Text and Data Mining for Biomedical Discovery
  96. International genome-wide meta-analysis identifies new primary biliary cirrhosis risk loci and targetable pathogenic pathways
  97. Testing multiple hypotheses through IMP weighted FDR based on a genetic functional network with application to a new zebrafish transcriptome study
  98. Understanding multicellular function and disease with human tissue-specific networks
  99. Adapting bioinformatics curricula for big data
  100. Targeted exploration and analysis of large cross-platform human transcriptomic compendia
  101. Systems Level Analysis of Systemic Sclerosis Shows a Network of Immune and Profibrotic Pathways Connected with Genetic Polymorphisms
  102. Testing multiple hypotheses through IMP weighted FDR based on a genetic functional network with application to a new zebrafish transcriptome study
  103. Big Data Bioinformatics
  104. Predicting targeted drug combinations based on Pareto optimal patterns of coexpression network connectivity
  105. Computational genetics analysis of grey matter density in Alzheimer’s disease
  106. Defining cell-type specificity at the transcriptional level in human disease
  107. LT-IIb(T13I), a Non-Toxic Type II Heat-Labile Enterotoxin, Augments the Capacity of a Ricin Toxin Subunit Vaccine to Evoke Neutralizing Antibodies and Protective Immunity
  108. Functional Knowledge Transfer for High-accuracy Prediction of Under-studied Biological Processes
  109. Time-Point Specific Weighting Improves Coexpression Networks from Time-Course Experiments
  110. Chapter 2: Data-Driven View of Disease Biology
  111. IMP: a multi-species functional genomics portal for integration, visualization and prediction of protein functions and networks
  112. Accurate evaluation and analysis of functional genomics data and methods
  113. PILGRM: an interactive data-driven discovery platform for expert biologists
  114. Evolving hard problems: Generating human genetics datasets with a complex etiology
  115. An Open-Ended Computational Evolution Strategy for Evolving Parsimonious Solutions to Human Genetics Problems
  116. An Analysis of New Expert Knowledge Scaling Methods for Biologically Inspired Computing
  117. Integrative Systems Biology for Data-Driven Knowledge Discovery
  118. Multifactor dimensionality reduction for graphics processing units enables genome-wide testing of epistasis in sporadic ALS
  119. Fast genome-wide epistasis analysis using ant colony optimization for multifactor dimensionality reduction analysis on graphics processing units
  120. Spatially Uniform ReliefF (SURF) for computationally-efficient filtering of gene-gene interactions
  121. Failure to Replicate a Genetic Association May Provide Important Clues About Genetic Architecture
  122. Sensible initialization using expert knowledge for genome-wide analysis of epistasis using genetic programming
  123. Nature-inspired algorithms for the genetic analysis of epistasis in common human diseases: Theoretical assessment of wrapper vs. filter approaches
  124. Development and evaluation of an open-ended computational evolution system for the creation of digital organisms with complex genetic architecture
  125. Optimal Use of Expert Knowledge in Ant Colony Optimization for the Analysis of Epistasis in Human Disease
  126. Environmental noise improves epistasis models of genetic data discovered using a computational evolution system
  127. Accelerating epistasis analysis in human genetics with consumer graphics hardware
  128. Ability of epistatic interactions of cytokine single‐nucleotide polymorphisms to predict susceptibility to disease subsets in systemic sclerosis patients
  129. Solving complex problems in human genetics using GP
  130. LTR Retrotransposon-Gene Associations in Drosophila melanogaster
  131. Solving Complex Problems in Human Genetics using Nature-Inspired Algorithms Requires Strategies which Exploit Domain-Specific Knowledge
  132. Ant Colony Optimization for Genome-Wide Genetic Analysis
  133. Relief-based bioinformatics methods for the analysis of epistasis in genetic association studies.