All Stories

  1. standard-GEM: standardization of open-source genome-scale metabolic models
  2. Systems Biology in ELIXIR: modelling in the spotlight
  3. The future of food and nutrition in ELIXIR
  4. Matching mouse models to specific human liver disease states by comparative functional genomics of mouse and human datasets
  5. ELIXIR and Toxicology: a community in development
  6. ELIXIR‐EXCELERATE: establishing Europe's data infrastructure for the life science research of the future
  7. The ELIXIR Human Copy Number Variations Community: building bioinformatics infrastructure for research
  8. PlaToLoCo: the first web meta-server for visualization and annotation of low complexity regions in proteins
  9. A community proposal to integrate structural bioinformatics activities in ELIXIR (3D-Bioinfo Community)
  10. Studies on the Mechanism of Chromosome Banding
  11. Community curation of bioinformatics software and data resources
  12. An intrinsically disordered proteins community for ELIXIR
  13. Disentangling the complexity of low complexity proteins
  14. Introducing the Brassica Information Portal: Towards integrating genotypic and phenotypic Brassica crop data
  15. PIsCO: A Performance indicators framework for collection of bioinformatics resource metrics
  16. PIsCO: A Performance indicators framework for collection of bioinformatics resource metrics
  17. Developing a strategy for computational lab skills training through Software and Data Carpentry: Experiences from the ELIXIR Pilot action
  18. ELIXIR-UK role in bioinformatics training at the national level and across ELIXIR
  19. BioCIDER: a Contextualisation InDEx for biological Resources discovery
  20. An open and transparent process to select ELIXIR Node Services as implemented by ELIXIR-UK
  21. Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics
  22. Circles within circles: commentary on Ghosal et al. (2013) “Circ2Traits: a comprehensive database for circular RNA potentially associated with disease and traits”
  23. Commentary on Shimoyama et al. (2012): three ontologies to define phenotype measurement data
  24. Phenomics
  25. Phenomics of the Laboratory Mouse
  26. Editorial: biological ontologies and semantic biology
  27. Biological Ontologies and Semantic Biology
  28. Analyzing gene expression data in mice with the Neuro Behavior Ontology
  29. Mouse Genetic and Phenotypic Resources as Tools for Human Genetics
  30. A tale of two drug targets: the evolutionary history of BACE1 and BACE2
  31. A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains
  32. Functional modelling of planar cell polarity: an approach for identifying molecular function
  33. Low microsatellite frequencies in neuron and brain expressed microRNAs
  34. Integration of global resources for human genetic variation and disease
  35. CASIMIR & ENFIN
  36. Protein coalitions in a core mammalian biochemical network linked by rapidly evolving proteins
  37. A Gene-Phenotype Network for the Laboratory Mouse and Its Implications for Systematic Phenotyping
  38. Towards BioDBcore: a community-defined information specification for biological databases
  39. Sustaining the Data and Bioresource Commons
  40. Identification of a Z-band associated protein complex involving KY, FLNC and IGFN1
  41. Phenotype ontologies for mouse and man: bridging the semantic gap
  42. XGAP: a uniform and extensible data model and software platform for genotype and phenotype experiments
  43. The Functional Annotation of Mammalian Genomes: The Challenge of Phenotyping
  44. EuroPhenome: a repository for high-throughput mouse phenotyping data
  45. MouseBook: an integrated portal of mouse resources
  46. Post-publication sharing of data and tools
  47. Entity/quality-based logical definitions for the human skeletal phenome using PATO
  48. Mouse, man, and meaning: bridging the semantics of mouse phenotype and human disease
  49. Planning the Human Variome Project: The Spain report
  50. Practical application of ontologies to annotate and analyse large scale raw mouse phenotype data
  51. Tandem and cryptic amino acid repeats accumulate in disordered regions of proteins
  52. Phylogenetic inference under recombination using Bayesian stochastic topology selection
  53. CASIMIR: Coordination and Sustainability of International Mouse Informatics Resources
  54. Digital preservation - financial sustainability of biological data and material resources
  55. The Mouse Resource Browser (MRB) - A near-complete registry of mouse resources
  56. Promoting coherent minimum reporting guidelines for biological and biomedical investigations: the MIBBI project
  57. Solutions for data integration in functional genomics: a critical assessment and case study
  58. Phenobabelomics--mouse phenotype data resources
  59. EuroPhenome and EMPReSS: online mouse phenotyping resource
  60. Integration of mouse phenome data resources
  61. Phenostat: visualization and statistical tool for analysis of phenotyping data
  62. A kinetic core model of the glucose-stimulated insulin secretion network of pancreatic β cells
  63. Integration of mouse phenome data resources
  64. Understanding Mammalian Genetic Systems: The Challenge of Phenotyping in the Mouse
  65. Gene factories, microfunctionalization and the evolution of gene families
  66. EMPReSS: European Mouse Phenotyping Resource for Standardized Screens
  67. Simple sequence repeats in proteins and their significance for network evolution
  68. CRAVE: a database, middleware and visualization system for phenotype ontologies
  69. B ayesian Analysis ( B ayes' Theorem)
  70. Bioinformatics.org
  71. CINEMA
  72. Cons I nspector
  73. DALI
  74. DNA Replication
  75. Decision Tree
  76. BLAT (BLAST-like Alignment Tool)
  77. Bioinformatics (Computational Biology)
  78. Complement
  79. DNA Sequence
  80. Organization and Evolution of a Gene-Rich Region of the Mouse Genome: A 12.7-Mb Region Deleted in the Del(13)Svea36H Mouse
  81. Dictionary of Bioinformatics and Computational Biology
  82. A bigger mouse? The rat genome unveiled
  83. Ontologies for the Description of Mouse Phenotypes
  84. A phylogenetic approach to assessing the significance of missense mutations in disease genes
  85. PlantProm: a database of plant promoter sequences
  86. Rapid restructuring of bicoid-dependent hunchback promoters within and between Dipteran species: implications for molecular coevolution
  87. How Slippage-Derived Sequences Are Incorporated into rRNA Variable-Region Secondary Structure: Implications for Phylogeny Reconstruction
  88. A Common Binding Site on the Microsomal Triglyceride Transfer Protein for Apolipoprotein B and Protein Disulfide Isomerase
  89. The structure of vitellogenin provides a molecular model for the assembly and secretion of atherogenic lipoproteins 1 1Edited by A. R. Fersht
  90. Trinucleotide Expansion Diseases in the Context of Micro- and Minisatellite Evolution. Hammersmith Hospital, April 1-3, 1998
  91. Modelling the secondary structures of slippage-prone hypervariable RNA regions: the example of the tiger beetle 18S rRNA variable region V4
  92. Simple sequences and the expanding genome
  93. Codon repeats in genes associated with human diseases: fewer repeats in the genes of nonhuman primates and nucleotide substitutions concentrated at the sites of reiteration.
  94. [38] Detection and quantification of concerted evolution and molecular drive
  95. A structural model of 5S RNA from E. coil based on intramolecular crosslinking evidence
  96. ENFIN - An Integrative Structure for Systems Biology