Our next Free, Live Webinars

When using reference data from the HapMap or 1000 Genomes Project, it is possible to accurately impute very large number of new SNPs for each subject. These new SNPs may be better surrogates than SNPs in the chip, or even causal variants, giving superior results in association analysis. Some experts even recommend re-analyzing all the performed GWAS with this new method.

In this live, free webinar, we'll give an overview of the BC|SNPmax data management and analysis platform, and demonstrate how to easily impute more genotypes and run analysis to create an efficient workflow for GWAS 2.0.

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March 31st, 10:00am PDT / 1:00pm EDT and 12:00pm GMT
Performing Re-sequencing Projects using the BC|SEQUENCE Data Management and Analysis Platform

As the cost of next-generation sequencing drops, carrying out re-sequencing projects is becoming increasingly feasible in many research projects. In this live, free webinar, we introduce the BC|SEQUENCE, which provides all the required tools for performing re-sequencing projects. In re-sequencing projects, new SNPs in interesting genome areas, such as candidate genes or exons, are first detected, then genotyped in a large cohort for association analysis.

In this webinar, we'll give an overview of the BC|SEQUENCE data management and analysis platform, and demonstrate how SNP detection, calling and detection of structural variations from next-generation sequence short read data is done. For running actual data analysis, we'll also introduce the different types of association analysis, population stratification and result visualization tools supported by BC|SEQUENCE. We'll also address some special issues of plant and animal sequencing and data analysis.

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