Multi-sample somatic variant caller
visual analysis of your VCF files
El genoma pequeño - analysis workflow for "the little genome." This repository holds a computational workflow to analyze the mitochondrial genome.
acorn is an R package that examines various features of de novo variants including subsetting DNVs by individual, variant type, or genomic region; calculating features including variant change counts, lengths, and presence/absence at CpG sites; and characteristics of parental age and number of DNVs.
Bundle of Useful scRNA-seq Gating Tools Extending seuRat
A/B testing (or split-testing) is a randomized experiment with two variants A and B. It includes application of statistical hypothesis testing (or two-sample hypothesis testing), as used in the field of statistics. A/B testing is a way to compare two versions of a single variable, typically by testing a subject's response to variant A against va…
Simulation of COVID-19 cases arising from high-risk contacts
Automatic annotation generation of the Variants in the VCF file into a text file
ShinyApp repo for the CovidTracker, any details further than the codes here available please send an email to rafael.lopes at yale.edu
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