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Beyond the E-Value: Stratified Statistics for Protein Domain Prediction.
Ochoa, Alejandro; Storey, John D; Llinás, Manuel; Singh, Mona.
Afiliación
  • Ochoa A; Department of Molecular Biology, Princeton University, Princeton, New Jersey, United States of America.
  • Storey JD; Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, New Jersey, United States of America.
  • Llinás M; Center for Statistics and Machine Learning, Princeton University, Princeton, New Jersey, United States of America.
  • Singh M; Department of Molecular Biology, Princeton University, Princeton, New Jersey, United States of America.
PLoS Comput Biol ; 11(11): e1004509, 2015 Nov.
Article en En | MEDLINE | ID: mdl-26575353
ABSTRACT
E-values have been the dominant statistic for protein sequence analysis for the past two decades from identifying statistically significant local sequence alignments to evaluating matches to hidden Markov models describing protein domain families. Here we formally show that for "stratified" multiple hypothesis testing problems-that is, those in which statistical tests can be partitioned naturally-controlling the local False Discovery Rate (lFDR) per stratum, or partition, yields the most predictions across the data at any given threshold on the FDR or E-value over all strata combined. For the important problem of protein domain prediction, a key step in characterizing protein structure, function and evolution, we show that stratifying statistical tests by domain family yields excellent results. We develop the first FDR-estimating algorithms for domain prediction, and evaluate how well thresholds based on q-values, E-values and lFDRs perform in domain prediction using five complementary approaches for estimating empirical FDRs in this context. We show that stratified q-value thresholds substantially outperform E-values. Contradicting our theoretical results, q-values also outperform lFDRs; however, our tests reveal a small but coherent subset of domain families, biased towards models for specific repetitive patterns, for which weaknesses in random sequence models yield notably inaccurate statistical significance measures. Usage of lFDR thresholds outperform q-values for the remaining families, which have as-expected noise, suggesting that further improvements in domain predictions can be achieved with improved modeling of random sequences. Overall, our theoretical and empirical findings suggest that the use of stratified q-values and lFDRs could result in improvements in a host of structured multiple hypothesis testing problems arising in bioinformatics, including genome-wide association studies, orthology prediction, and motif scanning.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteínas / Modelos Estadísticos / Estructura Terciaria de Proteína / Biología Computacional Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: PLoS Comput Biol Asunto de la revista: BIOLOGIA / INFORMATICA MEDICA Año: 2015 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteínas / Modelos Estadísticos / Estructura Terciaria de Proteína / Biología Computacional Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: PLoS Comput Biol Asunto de la revista: BIOLOGIA / INFORMATICA MEDICA Año: 2015 Tipo del documento: Article País de afiliación: Estados Unidos