escience and Post-Genome Biomedical Research



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escience and Post-Genome Biomedical Research Thomas L. Casavant, Adam P. DeLuca Departments of Biomedical Engineering, Electrical Engineering and Ophthalmology Coordinated Laboratory for Computational Genomics (CLCG) Center for Bioinformatics and Computational Biology (CBCB) http://genome.uiowa.edu 1

Outline 1. General Observations about Postgenomic escience 1. Specific Case Study where Traditional Publication and Archiving Practices are Lacking 1. Impact of Emerging Technology on Scale of the escience Problems 2

Post-Genomic escience The Post-Genome Era 3 Primary Types of Investigation 1. Generation of New High-Throughput Data (new Genome Projects ) 2. Generating New Data in the Context of Existing Results (Published or in Databases) 3. No New Data Exclusive re-use of Published Data 3

Case Study: Genomic Rearrangements or Deletions/Duplications (Dr. Krishna Rani Kalari, Mayo Clinic) 1. Goal: Identification of Human disease causing mutations 2. Observation: Assays exist to identify deletions and duplications time consuming laborious expensive 3. Approach: Develop In-silico procedures to identify and prioritize candidate deletion/duplication sites and accelerate the finding of disease mutation discovery 4

Approach Details 1. Construct case and control data sets for all known cases of disease causing unequal recombinations 2. Identify and obtain informative sequencebased features to create a training set 3. Evaluate machine learning methods on the training set 4. Design and develop a computational system to identify and prioritize candidate intragene deletions and duplications 5

Approach - System Level Obtain list of genes that have deletions/duplications Identify candidates From Published Literature Collect all the breakpoint sequences Case sequences Obtain annotation, melting Temperature and hapmap features for the DNA sequences Control sequences System/Analysis Predict deletion or duplication candidates 6

HGMD statistics 2362 genes have 64251 mutations 7 % (4,500) of the mutations in HGMD are caused by gross deletions and duplications. 7

HGMD mutation classification Mutation type Nucleotide substitutions (missene / nonsense) Total number of mutations Nucleotide substitutions (splicing) 46 Nucleotide substitutions (regulatory) 0 Small deletions 52 Small insertions 12 Small indels 1 Gross deletions 2 Gross insertions and duplications 0 Complex rearrangements (inversions) 1 Repeat variations 0 294

HGMD - Gross deletions Accession Number Description Phenotype Reference CG035110 ex. 18 (described at genomic DNA level) CG994802 36 bp nt. 6543 (described at genomic DNA level) Stargardt disease Yatsenko (2003) Hum Mutat 21, 636 Stargardt disease Lewis (1999) Am J Hum Genet 64, 422

Local Deletion Database 10

Of the 4,500 Possible Training Cases, How Many Did We Get??? Searched for specific break point information for 1463 IDDs described in HGMD Identified 102 fully-characterized rearrangement breakpoints (cases) know exactly where the breakpoint occurs Identified 2338 matching set of breakpoints for each of the positives for which IDDs have not been observed (controls) 11

SPeeDD web-interface 12

Lessons From Deletion Case Study Important results and data are buried in traditional forms of scientific publication and dissemination mechanisms (no surprise here). Fidelity and throughput of legacy results inadequate Necessary data can be requested from investigators In some cases Reference to a changing world of what is assumed to be known Stay tuned the problem will only get worse 13

Impact of Emerging Technology on Scale of the escience Problems 14

~3 genomes/week Genomes Online Database v2.0 www.genomesonline.org 15

How did we get here? Advances in genome sequencing were driven by the Human Genome Project Scale-up started in 1999 Resources concentrated in large genome centers Increase in capacity Reduction in cost Economies of scale Improved technology Sequencing infrastructure available for non-human projects 16

Genome Center Perspective (George Weinstock, Wash-U/Baylor GSCs) Research is Data-driven Produce more data Hypothesis generating > hypothesis testing Community resource projects Rapid data release; prepublication Etiquette in use of prepublication data No intellectual property contraints Production is Technology-enabled Develop or acquire new technologies 17

130:1

Human disease study 500 cases + 500 controls 500 genes, 15 exons/targets per gene 2 reads/target 15 million reads to screen 1,000 subjects 454: 10M rds/d or Solexa: 160M rds/d Conclusion: this is a small experiment 19

Project Jim Whole human genome Proof of Principle What can be learned from a single genome? What biases exist in the data? What analysis issues arise? Not a consensus sequence but need to capture both alleles: 6 GB not 3 GB Data quality vs variation: how do you know a variant base is a mutation and not an error 20

Conclusions: Post-genomic escience 1. Generation of New High-Throughput Data (new Genome Projects ) 2. Generating New Data in the Context of Existing Results (Published or in Databases) 3. No New Data Exclusive re-use of Published Data 21