Service

  1. Data management, logistics
  2. Genome assembly
  3. Transcript quantification
  4. Single cell analysis
  5. Variant calling
  6. Genotype imputation
  7. Phylogenetic analysis

Clinical records, Illumina, Olinks, Nanostring, Clariom etc.

  1. Exploratory analysis and visualization
  2. Differential expression
  3. Adjustment for multiple testing
  4. Survival and other endpoints analysis
  5. Mendelian randomization
  6. Diagnostic test performance
  7. Meta-analysis
  1. Sample size and power analysis
  2. Validation cohorts
  3. Diagnostic test development
  4. Companion diagnostics
  5. Adaptive trial design
  1. Molecular subtype discovery
  2. Biomarker discovery and validation, ReMARK, IVDMIA complianceĀ  etc.
  3. Functional impact of sequence variants
  4. Time series and forecasting
  1. Pathway enrichment
  2. Functional annotation of experimental results
  3. Data integration from omics platforms
  4. Text mining
  5. Complexity estimation
  6. Causative inference
  7. Network construction and annotation