IGH partitioning evaluation tool: Evaluations are performed against individual genotypes inferred from high throughput sequencing (as described in Boyd, 2010). To use the evaluation tool, obtain the Stanford_S22 dataset and perform IGH partitioning using the utility of your choice. Sets of results for the Stanford_S22 dataset, generated using a number of IGH utilities, are available on the datasets page, along with links to access the various utilities. The partitioning results produced by a utility can then be compared to an inferred genotype by either pasting results into the text box below, or indicating a file for upload. The formatting requirements for input files a file are described here. The evaluation tool will provide details of the allocation of genes and allelic variants absent from the inferred genotype for the IGHV, IGHD and IGHJ. References:
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