Summary of Projects, 2017
Combining omics & histopathology analysis to investigate the clinical phenotypes in ovarian cancer
Predictive capacity of secondary genetic findings: sensitivity analysis of Bayesian methods for the estimation of penetrance
Identifying candidate drugs to control bacterial persistence in mycobacterium tuberculosis using KsRepo
Mutations associated with drug resistance in tuberculosis
Inferring clonal loss of heterozygosity regions from scRNA-seq data
Developing data visualization & statistical analysis utilities for the PAGODA2 platform
Metagenome-wide Association Study Resources: Statistical Analysis R Package & Metagenomic Data Catalogue
Variation in clinical phenotypes and relevance to medical decision-making
Analysis of differential chromatic accessibility during Drosophila mesoderm differentiation
Investigating bispecific DNA binding of the CHES-1-like protein
Challenges in mutational signature detection
Identifying somatic structural variants in neurotypical individuals
Somatic mutation balance & single cell sequencing in heterochromatic: X chromosome inactivation as a model
Rare disease case analysis: Identifying potential novel gene candidates
Redesigning the patient portal: A use case of the SMART on FHIR platform to improve health literacy
Pipeline characterization of unique autosomal random monoallelic expression patterns in MAE genes
Genomic tool for predicting monoallelic expression using epigenetic signature