THE GENOME ACCESS COURSE (TGAC)
November 13 - 15, 2017
Cold Spring Harbor Laboratory, New York
This course is now full
All registrations received after August 23rd will be automatically waitlisted
Benjamin King, University of Maine
Delphine Fagegaltier, The New York Genome Center
Emily Hodges, Vanderbilt University School of Medicine
Steven Munger, The Jackson Laboratory
The Genome Access Course is an intensive two-day introduction to bioinformatics. Participants are expected to arrive by 6 p.m. on the first day (November 13) with the course running two full days until 5 p.m. on the third day (November 15).
The course is broken into modules that are each designed to give a broad overview of a given topic, with ample time for examples chosen by the instructors. Each module features a brief lecture describing the theory, methods and tools followed by a set of worked examples that students complete. Students are encouraged to engage instructors during the course with specific tasks or problems that pertain to their own research.
The core of the course is the analysis of sequence information framed in the context of completed genome sequences. Featured resources and examples primarily come from mammalian species, but concepts can be applied to any species. The course also features methods to assist the analysis and prioritization of gene lists from large scale microarray gene expression and proteomics experiments. Summaries of the topics are listed below.
Sequence, Gene, and Protein Resources
NCBI Sequence, Gene, and Protein Resources
Model Organism Databases: Mouse Genome Informatics, Rat Genome Database, ZFIN, FlyBase
Protein Sequence and Domain Resources: UniProt, PDB, InterPro
Proteomics Resources: IPI, ExPaSY, PRIDE
microRNA Resources: miRBase, microCosm Targets, TargetScan, PicTar
Repositories of High-Throughput Sequence Data
Repositories of Gene Expression Data: GEO, ArrayExpress
Gene Expression Profiling Resources
Genome Sequencing and Assembly
Overview and Comparison of Major Genome Browsers: Ensembl, UCSC, NCBI Map Viewer
Adding custom tracks
Bulk genome retrieval tools: BioMart, UCSC Table Browser
de novo Analysis of Sequences
Local, Global, Pairwise, and Multiple Sequence Alignments
BLAST and BLAT Algorithms
Scoring Matrices: PAM, BLOSUM
Iterative Profile and Pattern Searches
Multiple Sequence Alignment Programs
Visualizing & Editing Multiple Alignments
Types of Sequence and Structural Variation
SNP Resources: dbSNP
Structural Variation Resources: dbVar, DGVa, HGVbase
Comparative Genome Analysis and Functional Genomic Elements
Finding Putative Regulatory Elements in Genome Sequence by Comparing Genomes
Ortholog and Paralog Resources
Multicontigview in Ensembl
Comparative Tracks in the UCSC Genome Browser
DCODE and ENCODE Resources
Analysis of High-Throughput Sequence Data
Common File Formats: FASTQ, SAM, BAM
Quality Control and Diagnostic Analyses
Mapping Reads To a Reference Sequence
Finding Putative Mutations and Polymorphisms
RNA-Seq Data Analysis
ChIP-Seq Data Analysis
de novo Assembly
Gene Set Enrichment and Pathway Analysis
Prioritizing Genes from Microarray and Proteomics Experiments
Gene Set Enrichment Analysis Tools: GSEA, DAVID
Pathway Resources: Reactome, HPRD NetPath, KEGG
Protein Interaction Resources: MIPS, MINT, BIND, DIP
Each student will be provided with a laptop (if needed) and internet access for the duration of the course. You can also bring your own laptop to the course provided it meets the following requirements: 1) a standard browser (Internet Explorer, Firefox, etc.) that is up-to-date with security patches and bug fixes, 2) wireless internet capacity, and 3) the ability to view and modify plain text files and spreadsheets (e.g., Microsoft Word and Excel). Both PCs and Macs are acceptable as long as they're updated with all security patches and bug fixes.
The Genome Access Course is open to all on a first-come, first-served registration system. It is most beneficial for bench scientists transitioning into projects that require intensive analysis or integration of large data sets. The course will introduce you to publicly available resources, and it will also help you develop a vocabulary that can be used to collaborate with computational scientists. If you already have significant programming or data analysis experience, this course is not appropriate for you. For more detailed curriculum on methods used in computational biology, please see the Foundations of Computational Genomics course. Students interested in the practical aspects of software development are encouraged to apply to the course on Programming for Biology. Students who would like in-depth training in the analysis of next-generation sequencing data (e.g., genome assembly and annotation, SNP calling, and the detection of structural variants) may be interested in the course on Advanced Sequencing Technologies & Applications. Finally, please see the course on Statistical Methods for Functional Genomics if you would like training in the statistical analysis of high-throughput genomics data.
The curriculum of The Genome Access Course has been developed in conjunction with staff at the Wellcome Trust Sanger Institute and the European Bioinformatics Institute (Hinxton, UK) who teach a parallel series of courses in the UK; see the Open Door Workshops for more information.
Major support provided by the Helmsley Charitable Trust. Limited financial aid is available; please apply in writing to the course registrar describing your need for financial support.
Academic Package (two nights of housing) $1,050
Corporate Package (two nights of housing) $1,750
Academic No-Housing Package $740
Corporate No-Housing Package $1,320
Extra nights at $260 per night
All packages cover registration, food, coffee breaks, and a reception. Transportation to and from Cold Spring Harbor is not included. Full payment is due three weeks prior to the course.