Software for Rapid Analyses of Human Copy Number Data
X chromosome regional variation by population
This project analyzes X chromosome data to study the association between red and green gene configurations and color blindness. It aligns sequencing reads to the reference sequence, maps them to gene exons, and determines the most likely configuration causing color blindness.
🧬 recombination and mutation rates inference from polymorphisms (STRs, SNPs and INDELs) along the X chromosome
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