Apply November 1, 2017 – January 31, 2018
- Metagenomic and metatranscriptomic analysis of bacterial strains using PanPhlAn Software
- Exome Sequencing identifies a novel mutation in MED12 as potential cause of severe birth defects in a female
- Website development for visualization of Hi-C Data
- Identifying monoallelic expression using epigenetic signatures in silico
- Understanding rare Mendelian genetics diseases through sequencing
- Geo-temporal database for the external exposome
- Analyzing discrepancies in the International Cancer Genome Consortium with UpSetR
- Role of transcription factors in recruiting non-specific DNA binding proteins
- Optimizing of tile generation for HI-C data
- Visualizing geographic trends in insurance claims data
- Accurate estimation of molecular counts in droplet-based single-cell RNA-seq experiments
- Benchmarking biomedical word embeddings
- Characterizing insulated neighborhoods in esophageal cancer patients
- Using diverse population sequencing data to estimate penetrance for the ACMG-56 panel
- Comparison of single-cell RNA-seq trajectory construction methods