Steve Greenham
Panel Discussion Session
The 1000 Genomes Project and challenges in population-scale sequencing
Prospects for pharmacogenetics in a genome-sequencing era
Should I sequence my genome now?
Genome-wide characteristics of sequence coverage by next-generation sequencing: how does this impact interpretation?
Allele specific expression analysis using high throughput DNA sequencing
Cis-regulatory SNPs (cis-rSNPs) altering transcription detected by allelic expression (AE) mapping
Identification of enriched regions in ChIP-seq and whole-genome sequencing data
Species specific transcription in mice carrying human chromosome 21
A statistical framework for the analysis of ChIP-Seq data
Microevolutionary analysis of metagenomic data
Understanding variation in mRNA processing with RNA sequencing
Deconvolving the epigenome: analysis strategies for genome-wide studies
Analysis of whole cancer genomes
Statistical models for inference of SNVs in cancer genomes
Phasing SNPs and sequences
Genotype imputation with thousands of genomes
Reference-free analysis of genetic variation
Efficient construction of overlap assemblies using suffix array based methods
Calling small indels in the 1000 Genomes low-coverage and high-coverage pilots
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