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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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Bibliographic Details
Main Authors: Keightley, Peter D., Halligan, Daniel L.
Format: Artigo
Language:Inglês
Published: Genetics Society of America 2011
Subjects:
Online Access: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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