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Video and slides from ASHG 1000 Genomes tutorials

If you missed the tutorial on the 1000 genomes project data last week at ASHG, you can now watch the tutorials on youtube and download the slides online at http://genome.gov/27542240. Here's a recap of the speakers and topics:

Introduction
Gil McVean, Ph.D.
Professor of Statistical Genetics
University of Oxford

Description of the 1000 Genomes Data
Gabor Marth, D.Sc.
Associate Professor of Biology
Boston College

How to Access the Data
Steve Sherry, Ph.D.
National Center for Biotechnology Information
National Library of Medicine
National Institutes of Health. Bethesda, Md.

How to Use the Browser
Paul Flicek, Ph.D.
European Molecular Biology Laboratory
Vertebrate Genomics Team
European Bioinformatics Institute (EBI)

Stuctural Variants
Jan Korbel, Ph.D.
Group Leader, Genome Biology Research Unit
Joint Appointment with EMBL-EBI
European Molecular Biology Laboratory (Heidelberg, Germany)

How to Use the Data in Disease Studies
Jeffrey Barrett, Ph.D.
Team Leader, Statistical and Computational Genetics
Wellcome Trust Sanger Institute
Hinxton, United Kingdom

Visit http://genome.gov/27542240 for links to all the videos and slides. I found Jeff Barrett's overview of using the 1000 genomes data for imputation particularly helpful. Also, don't forget about Goncalo Abecasis's 1000 genomes imputation cookbook, which gives a little more detailed information about formatting, parallelizing code, etc. I'm going to be trying this myself soon, and I'll post tips along the way.



Keep up with what's happening at ASHG 2010

As this year's ASHG meeting starts to wind down be sure to check out Variable Genome where Larry Parnell is summarizing what's going on at the talks he's been to. Also see the commentary on Genetic Inference by Luke Jostins. The 1000 Genomes tutorial from Wednesday night will be made available on genome.gov soon, and the presidential address, plenary sessions, and distinguished speaker symposium talks were recorded and will also soon be online. You can keep up with what's going on in real time by following the #ASHG2010 tag on Twitter.

Reproducible Research in the Omics Era: A Presentation and Panel Discussion

Seminar announcement for Vanderbilt folks:


Vanderbilt-Ingram Cancer Center
Quantitative Sciences Seminar Series

Presents

Reproducible Research in the Omics Era:
A Presentation and Panel Discussion
Kevin R. Coombes, PhD
Deputy Chair, Bioinformatics, and Professor of Bioinformatics and
Computational Biology
M.D. Anderson Cancer Center

and

Keith Baggerly, PhD
Associate Professor, Dept. of Bioinformatics and Computational Biology
M.D. Anderson Cancer Center


Panel Discussion at 1 p.m., following presentations:
Featuring Drs. Baggerly and Coombes, along with
Vanderbilt University School of Medicine’s
Dr. William Pao, Dr. Frank Harrell, and Dr. Yu Shyr

Friday, November 19, 2010
12 noon – 2 PM
214 Light Hall


PacBio Film, Discussion & Reception/Dinner at ASHG 2010

Pacific Biosciences is hosting a reception and dinner, and is screening their film The New Biology at this year's ASHG meeting. According to a flyer the mailed me, the film will showcase their SMRT sequencing technology and how it can be used to "create predictive models of living systems and gain wisdom about the fundamental nature of life itself." While the last bit is perhaps an overstatement, the event should nonetheless be an event worth attending. The event includes a reception, dinner, and a moderated discussion featuring individuals from the film. Unfortunately this conflicts with the previously mentioned 1000 Genomes Tutorial, but if you get waitlisted at the tutorial, sign up for this event at the link below!

Date
Wednesday, November 3 2010

Time
7-10pm

Location
Smithsonian National Air and Space Museum
Independence Ave at 6th St SW
Washington, DC 20560

RSVP here - pacificbiosciences.com/newbiology

Prioritizing GWAS Results: A Review of Statistical Methods and Recommendations for Their Application

While writing my thesis I came across this nice review by Rita Cantor, Kenneth Lange, and Janet Sinsheimer at UCLA, "Prioritizing GWAS Results: A Review of Statistical Methods and Recommendations for Their Application." Skip the introduction unless you're new to GWAS, in which case you'll probably want to start with this more recent review by Teri Manolio. After skipping the intro you'll find succinct introduction to meta-analysis for GWAS with lots of very good references, including these among others:

DerSimonian R., Laird N. Meta-analysis in clinical trials. Control. Clin. Trials. 1986;7:177–188. [PubMed]

Fleiss J.L. The statistical basis of meta-analysis. Stat. Methods Med. Res. 1993;2:121–145. [PubMed]

Yesupriya A., Yu W., Clyne M., Gwinn M., Khoury M.J. The continued need to synthesize the results of genetic associations across multiple studies. Genet. Med. 2008;10:633–635. [PubMed]

Lau J., Ioannidis J.P., Schmid C.H. Quantitative synthesis in systematic reviews. Ann. Intern. Med. 1997;127:820–826. [PubMed]

Allison D.B., Schork N.J. Selected methodological issues in meiotic mapping of obesity genes in humans: Issues of power and efficiency. Behav. Genet. 1997;27:401–421. [PubMed]

Ioannidis J.P., Gwinn M., Little J., Higgins J.P., Bernstein J.L., Boffetta P., Bondy M., Bray M.S., Brenchley P.E., Buffler P.A., Human Genome Epidemiology Network and the Network of Investigator Networks A road map for efficient and reliable human genome epidemiology. Nat. Genet. 2006;38:3–5. [PubMed]

de Bakker P.I., Ferreira M.A., Jia X., Neale B.M., Raychaudhuri S., Voight B.F. Practical aspects of imputation-driven meta-analysis of genome-wide association studies. Hum. Mol. Genet. 2008;17(R2):R122–R128. [PMC free article] [PubMed]

Sagoo G.S., Little J., Higgins J.P., Human Genome Epidemiology Network Systematic reviews of genetic association studies. PLoS Med. 2009;6:e28. [PMC free article] [PubMed]

Zeggini E., Ioannidis J.P. Meta-analysis in genome-wide association studies. Pharmacogenomics. 2009;10:191–201. [PMC free article] [PubMed]

Egger M., Smith G.D., Phillips A.N. Meta-analysis: Principles and procedures. BMJ. 1997;315:1533–1537. [PMC free article] [PubMed]

Ioannidis J.P., Patsopoulos N.A., Evangelou E. Heterogeneity in meta-analyses of genome-wide association investigations. PLoS ONE. 2007;2:e841. [PMC free article] [PubMed]

This section covers using imputation in meta-analysis, fixed effects versus random effects meta-analysis, canned software for meta-analysis (such as METAL), Bayesian hierarchical approaches, and references to many applications of meta-analysis in GWAS.

After the meta-analysis section there's a nice section on modeling epistasis, or gene-gene interactions, to prioritize associations with links to other reviews of statistical methods, and brief coverage of data mining procedures like CART, MDR, random forests, conditional entropy methods, neural networks, genetic programming, logic regression, pattern mining, Bayesian partitioning, and penalized regression approaches, again with lots of references. This section also covers parameterization of epistatic models, and covers some of the computation and statistical issues you'll face with the dimensionality problem.

Finally, the review concludes with a section on pathway analysis. As the review admits, pathway analysis in GWAS has no set of strict guidelines or best practices, and new approaches arise every day.

While this review is nearly a year old at this point, I think it's a real gem because of all the references it offers, especially in the meta-analysis and epistasis sections.

AJHG: Prioritizing GWAS Results: A Review of Statistical Methods and Recommendations for Their Application

Tutorial on the 1000 Genomes Project Data

There will be a (free) tutorial on the 1000 genomes project at this year's ASHG meeting on Wednesday, November 3, 7:00 – 9:30pm. You can register online at the link below. The tutorial will describe the 1000 genomes data, how to access it, and what to do with it. Specifically, the speakers and topics covered are:

1. Introduction
2. Description of the 1000 Genomes data -- Gabor Marth
3. How to access the data -- Steve Sherry
4. How to use the browser -- Paul Flicek
5. Structural variants -- Jan Korbel
6. How to use the data in disease studies -- Jeff Barrett
7. Q&A

Online registration for 1000 genomes tutorial

Hopefully I'll see some of you there. I'm not sure if imputation is covered in this tutorial. If not, I will cover it here in a future post. I'll soon be using Goncalo Abecasis's 1000 Genomes Imputation Cookbook to impute my own data to the 1kG SNPs, and I'll share any tips I discover along the way.

Random forests for high-dimensional genomics data

I know I've been MIA for a while. My defense date is December 3, and I've still got a thesis to write! I'll try to post more soon, but in the meantime follow me on Twitter for things that won't make it into a full blog post.

For those at Vanderbilt and the surrounding environs: I saw this announcement for the next cancer biostatistics workshop that looked interesting.

2010 Cancer Biostatistics Workshop

Friday, october 15, 2010
1:00 to 2:00 PM
898B Preston Research Building

Random forests for high-dimensional genomics data

Xi (Steven) Chen, PhD
Assistant Professor
Department of Biostatistics
Cancer Biostatistics Center, Vanderbilt-Ingram Cancer Center