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Workshops for teachers and researchers      

Workshop Descriptions

Workshop Resources

The resources used with each workshop are listed in the workshop description.

2004 Workshop Schedule

To arrange for workshop or course, contact: info@geospiza.com

BLAST for beginners

An introduction to sequence comparison using BLAST. This workshop usually includes a short description of "what is bioinformatics?", an overview of what BLAST does, and a hands-on activity where participants get a sequence from our web site, do a BLAST search, and answer questions about the sequence.

Tutorial: BLAST for beginners
Additional materials:
        BLAST worksheet
        DNA sequences of "unknown origin"


Finding genes with Entrez

An overview of various databases at NCBI and a discussion of strategies for finding information and determining if what you've found is what you were looking for. Participants brainstorm to identify genes of interest in plants and then use various strategies to find them in GenBank.

handouts:
        instructor version
        student version

Allelic Variants of Superoxide dismutase

This covers using NCBI's LocusLink and Genes and Disease to research different aspects of an inherited disease. Participants find information about Lou Gehrig's disease, use OMIM to find a list of alleles, and use Cn3D to identify where the mutations are located in the three dimensional structure of the enzyme superoxide dismutase, with the goal of trying to develop a hypothesis to explain why a particular amino acid change, affects the activity of the enzyme.

Tutorial: Allelic Variants of Human Superoxide Dismutase
Additional materials: SOD Variant worksheet

Learning about structure with Cn3D

Structure-viewing applications like Cn3D, RasMol, MAGE, and Chime, can help students visualize and understand differences between macromolecules like proteins and nucleic acids. The application used in this workshop, Cn3D, is is freely available from the National Center for Biotechnology Information (http://www.ncbi.nlm.nih.gov) and easy to use.
In this workshop, participants will use Cn3D to examine and distinguish between, the primary, secondary, and quaternary levels of protein structure and to compare the structures of proteins and nucleic acids.

Tutorial: Introduction to Protein Structure
Additional materials:
        Amino acid abbreviations ( 24kb)
        Amino acid structures (36kb)

Studying Maternal Inheritance Through Mitochondria

Mitochondrial DNA sequences are widely used as tools for identifying maternal ancestors and studying human migration. Workshop participants use mitochondrial sequences from different regions of the world to determine if they can confirm the origin of these sequences, and then identify the maternal origin of an unknown sequence.

Tutorial: Mitochondria and Chloroplasts - maternal inheritance
Additional materials:
        Maternal inheritance worksheet
        Maternal sequences of unknown origin
        Maternal Inheritance Answer Key - available at workshops

Mitochondria and Chloroplasts as Models of Genomic Biology

Mitochondria and chloroplasts have their own genomes and exist independently inside the cell.
The small size of their genomes and the limited number of proteins make them an excellent model for studying genomic biology. Workshop participants will review some facts about these organelles, come up with study questions, determine which questions can be answered with bioinformatics tools, and then use different types of bioinformatics tools to research the answers.

Tutorial: Mitochondria and Chloroplasts

SNP or Sequencing Error?

Single nucleotide polymorphisms, or SNPs, are responsible for most of the individual differences within a population. An extensive effort is underway to identify and catalog SNPs with one possible goal, the development of better diagnostic tools and individualized medicine. However, DNA sequencing is not error-free. How do we distinguish between a polymorphism and a sequencing mistake?

This workshop discusses some of the bioinformatics tools used in DNA sequencing and assembly, such as phred and phrap, and some strategies for discovering new SNPs. Workshop participants use bioinformatics tools to determine if sequencing discrepancies are likely to be SNPs or sequencing mistakes.

Tutorial: SNP or sequencing error?
Additional materials:
         Contig sequences and phrap quality graphs from four genes of medical importance


Funding for this project was provided by the National Science Foundation's Course, Curriculum, and Laboratory Improvement Program under grants DUE-0088153 and DUE-0127599, also from Bio-Link, an NSF Advanced Technology Education Center.

Any opinions, findings, and conclusions or recommendations expressed in this material are those of the author and do not necessarily reflect the views of the National Science Foundation.

 
 
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