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Inference of Site Frequency Spectra From High-Throughput Sequence Data: Quantification of Selection on Nonsynonymous and Synonymous Sites in Humans

Sequencing errors and random sampling of nucleotide types among sequencing reads at heterozygous sites present challenges for accurate, unbiased inference of single-nucleotide polymorphism genotypes from high-throughput sequence data. Here, we develop a maximum-likelihood approach to estimate the fr...

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Bibliografske podrobnosti
Main Authors: Keightley, Peter D., Halligan, Daniel L.
Format: Artigo
Jezik:Inglês
Izdano: Genetics Society of America 2011
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC3176106/
https://ncbi.nlm.nih.gov/pubmed/21596896
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1534/genetics.111.128355
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