Ali Mortazavi
Second Generation RNA-seq
Wold Lab at California Institute of Technology

Website

Bing Ren
From ChIP-chip to ChIP-Seq: Unraveling the Second Code of the Human Genome
UCSD

Website

David Craig
Identification of genetic variants within specific regions of the human genome
Translational Genomics Research Institute (TGen)

Website

Elaine Mardis
Human re-sequencing for variant discovery in cancer
Washington University

Website

Elliott Margulies
Informatics and Experimental Strategies for De Novo Genome Sequencing with Short Reads
National Human Genome Research Institute (NHGRI)

Website

Inanc Birol
De novo assembly of short reads as a discovery tool
BC Cancer Research Center

Website

Katherine Sorber
The long march: a sample preparation technique that enhances contig length and coverage by high-throughput short-read sequencing.
This technique has demonstrated utility in the resequencing of the Plasmodium falciparum transcriptome as well as in metagenomic analysis of a serum sample from a patient with hepatitis B virus (HBV)-related acute liver failure.
DeRisi Lab, UCSF

Website

Pavel Pevzner
EULER-USR: Assembling Short and error-Prone DNA Reads
UCSD

Website

Richard Cronn
Multiplex sequencing of organelle genomes using sequencing-by-synthesis technology: Insights from the first 100 plastomes
Pacific Northwest Research Station-USDA Forest Service

Website

Ryan Lister
Mapping the Arabidopsis Epigenome and Transcriptome by Deep Sequencing
Ecker Lab, Salk Institute

Website

Yaniv Ehrlich
Alta-Cyclic - A self optimizing base caller for Illumina Genome Analyzer.
Cold Spring Harbor Labs

Website

Hanlee Ji
Targeted Human Genome Resequencing
Stanford University Medical Center

Website