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In the forge results, the fraction correct may be the same overall at 0 and 100% SNP inclusion …is it better for some alleles/ genes and worse for others (what does the plot look like stratified by gene?) [Am I interpreting correctly? The dynamic range here looks very small .1%] how do the results change with structural variants? (And what are their relative frequency vs. SNPs?)How do reference based approaches compare to de novo assembly after noisy alignment?