ParAllele BioScience Products & Services


Overview Genotyping Services Genotyping Products Discovery Partnerships Ordering Support	Overview The MegAllele" genotyping products and services provide the most comprehensive way for researchers in genetics to perform association studies. These studies can be rapidly completed at multiple SNP densities using either custom-designed assay panels or standard assay panels to fit individual study requirements. You can now quickly generate accurate, reproducible, and comprehensive genotype results either through a full service or by early access to MegAllele genotyping products to run in your own lab. Applications include the following: Fine mapping one or more linkage peaks to find disease association Studying candidate genes in a cohort to pinpoint individual disease genes The ParAllele Discovery Partnerships provide the most comprehensive way for researchers to perform genetics studies. While other approaches are targeted primarily to the common disease/common variation hypothesis, our portfolio of innovative technologies enables the study of the full spectrum of rare and common genetic variation to comprehensively identify both high and low relative risk disease alleles.
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Overview

Genotyping Services

Genotyping Products

Discovery Partnerships

Ordering

Support

Overview

The MegAllele" genotyping products and services provide the most comprehensive way for researchers in genetics to perform association studies. These studies can be rapidly completed at multiple SNP densities using either custom-designed assay panels or standard assay panels to fit individual study requirements. You can now quickly generate accurate, reproducible, and comprehensive genotype results either through a full service or by early access to MegAllele genotyping products to run in your own lab.

Applications include the following:

Fine mapping one or more linkage peaks to find disease association
Studying candidate genes in a cohort to pinpoint individual disease genes

The ParAllele Discovery Partnerships provide the most comprehensive way for researchers to perform genetics studies. While other approaches are targeted primarily to the common disease/common variation hypothesis, our portfolio of innovative technologies enables the study of the full spectrum of rare and common genetic variation to comprehensively identify both high and low relative risk disease alleles.