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RHH is convenient to execute (e.g. in not requiring phased chromosomes or allele frequencies from ethnic panels) and RHH numerical and visual output is also easily understood by the non-specialist since it is transparent (i.e. counts and chromosomal locations of rare genotypes whose highest dataset frequencies are user-specified).
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The site is convenient to military families.
The subsequent consideration is more convenient to execute for p 1, p 2 momenta.
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That might be convenient to some.
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It's convenient to mass transit.
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