Golden Helix PBAT
Cutting-edge tools for family-based association studies
Golden Helix PBAT is an advanced statistical package for the design and analysis of family-based SNP and copy number variation (CNV) association studies. In addition to its extensive array of analysis methods, PBAT is acclaimed for its ability to overcome the multiple testing problem in whole genome association studies using cutting-edge screening methods.
Golden Helix PBAT is developed in collaboration with Dr. Christoph Lange of the Harvard School of Public Health.
- What's New
- Overview
- Getting Started
New Analysis Capabilities Make PBAT more Powerful and Comprehensive
Family-Based Copy Number Association Analysis
All robustness properties of the FBAT approach are maintained as in PBAT for SNP analysis. In addition, all previously-developed FBAT extensions, including FBATs for time-to-onset, multivariate FBATs, and FBAT-testing strategies, can be directly transferred to the analysis of copy number variations.
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Faster Extended Pedigree Analysis
A new optional algorithm is available that can make PBAT 10-100 times faster than the original implementation when analyzing large extended pedigrees. It can be applied to SNP, haplotype and copy number analysis.
See the following knowledge base article for more information:
Golden Helix PBAT Helps to Find a Whole Genome Age-Dependent Association between SNP rs1455832 and obesity
In a recent whole genome association study using the Affymetrix
100K scan of the Framingham Heart Study (FHS), Dr. Jessica
Lasky-Su et al used Golden Helix PBAT to find an age-dependent
association between SNP rs1455832 and obesity. The finding was
replicated in five of eight followup studies.
The paper titled On the Replication of Genetic Association: Timing Can Be Everything was published in the April 11, 2008 edition of American Journal of Human Genetics.
›› Read the abstract
What is Golden Helix PBAT?
Golden Helix PBAT provides tools for the design and analysis of family-based SNP and copy number association studies. It incorporates virtually all functionality of the family-based association tests (FBAT) package, but also provides additional options for designing association/linkage studies, analyzing data with multiple continuous traits, and screening for the most "promising" combinations of markers and phenotypes. |
Explore Further
Get Started Accelerating Your Quest for Significance!
The following resources are available to help you get started:
A more complete copy number association workflow
The following processing, analysis, and quality control measures have
been added recently to make the copy number association workflow more complete:
- Download Free Trial
- Whole Genome Association Tutorial
- Documentation
- Tutorials and Webinars
