Register by May 25 and Save up to $350!
Sequencing a genome is only the beginning. Several layers of analysis are necessary to convert raw sequence data into understanding of functional biology. First, error sources in the original raw data from multiple platforms and diverse applications must be accounted for. Then, as computational methods for assembly, alignment, and variation detection continue to advance, a broad range of genetic analysis applications including comparative genomics, high-throughput polymorphism detection, analysis of coding and non-coding RNAs, and identifying mutant genes in disease pathways can be addressed. CHI’s Next-Generation Sequencing Data Analysis conference combines unique perspectives from a variety of researchers, engineers, biostatisticians, and software developers involved in NGS data analysis
FEATURED SPEAKER:
Mark Gerstein, Ph.D., Albert L. Williams Professor of Biomedical Informatics, Molecular Biophysics and Biochemistry, Computer Science, Yale University
AGENDA TOPICS INCLUDE:
- Assembly’s Role in Gene Annotation
- Assembly and Alignment’s Role in Analysis
- Analysis: Structural Variation
- Analysis: RNA-Seq
HALF DAY SESSION FROM TODAY'S TOP SEQUENCING CENTERS!
Presentations from:
- The Broad Institute
- New York Genome Center
- Cold Spring Harbor
- Washington University
- Yale University
- J. Craig Venter Institute
