BC/SNPmax from Biocomputing Platforms is a data management solution for whole genome association studies. It integrates high-density SNP genotype data with phenotypes and maps, creating a highly productive data analysis pipeline with automated input file generation for analysis programs.
BC/SNPmax enhances the use of the best analysis programs for quality control, case/control analysis and family-based analysis. An advanced built-in queue system supports performing multiple, large parallel database transactions and calculation tasks. The queue system also makes it easier to build powerful calculation clusters.
A BC/SNPmax system can be implemented quickly, without requiring substantial resources for programming, allowing a research group’s programmers to focus on the top scientific priorities.
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All variations of Affymetrix SNP sets (10K, 100K, 500K, etc.) |
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High speed imports of native Affymetrix CHP file genotypes or GDAS Text Outputs |
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Automated error checking of genotype imports including mendelian errors |
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Custom exports to multiple analysis platforms |
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Fully functional sample tracking |
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Customizable database tracking both pedigrees and individuals, allowing unlimited custom data fields |
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Progeny Lab provides functionality to manage all clinical and lab data in one relational database |