Genome-wide significance testing of variation from single case exomes
Standard techniques from genetic epidemiology are ill-suited to formally assess the
significance of variants identified from a single case. We developed a statistical inference …
significance of variants identified from a single case. We developed a statistical inference …
Genome-wide significance testing of variation from single case exomes
AB Wilfert, KR Chao, M Kaushal, S Jain… - Nature …, 2016 - ohsu.elsevierpure.com
Standard techniques from genetic epidemiology are ill-suited to formally assess the
significance of variants identified from a single case. We developed a statistical inference …
significance of variants identified from a single case. We developed a statistical inference …
Genome-wide significance testing of variation from single case exomes
AB Wilfert, KR Chao, M Kaushal, S Jain… - Nature …, 2016 - pubmed.ncbi.nlm.nih.gov
Standard techniques from genetic epidemiology are ill-suited to formally assess the
significance of variants identified from a single case. We developed a statistical inference …
significance of variants identified from a single case. We developed a statistical inference …
Genome-wide significance testing of variation from single case exomes
AB Wilfert, KR Chao, M Kaushal, S Jain, S Zöllner… - Nature …, 2016 - profiles.wustl.edu
Standard techniques from genetic epidemiology are ill-suited to formally assess the
significance of variants identified from a single case. We developed a statistical inference …
significance of variants identified from a single case. We developed a statistical inference …
Genome-wide significance testing of variation from single case exomes
AB Wilfert, KR Chao, M Kaushal, S Jain, S Zollner… - Nature …, 2016 - go.gale.com
Donald Conrad and colleagues present a method, PSAP, for prioritizing potential Mendelian
disease-causing variants in single human exomes using pathogenicity scores and observed …
disease-causing variants in single human exomes using pathogenicity scores and observed …
[HTML][HTML] Genomewide significance testing of variation from single case exomes
AB Wilfert, KR Chao, M Kaushal, S Jain, S Zöllner… - Nature …, 2016 - ncbi.nlm.nih.gov
Standard techniques from genetic epidemiology are ill-suited to formally assess the
significance of variants identified from a single case. We developed a statistical inference …
significance of variants identified from a single case. We developed a statistical inference …
[PDF][PDF] Genomewide significance testing of variation from single case exomes
AB Wilfert, KR Chao, M Kaushal, S Jain, S Zöllner… - Nat Genet, 2016 - researchgate.net
Standard techniques from genetic epidemiology are ill-suited to formally assess the
significance of variants identified from a single case. We developed a statistical inference …
significance of variants identified from a single case. We developed a statistical inference …
Genome-wide significance testing of variation from single case exomes.
AB Wilfert, KR Chao, M Kaushal, S Jain, S Zöllner… - Nature …, 2016 - europepmc.org
Standard techniques from genetic epidemiology are ill-suited to formally assess the
significance of variants identified from a single case. We developed a statistical inference …
significance of variants identified from a single case. We developed a statistical inference …
Genome-wide significance testing of variation from single case exomes.
AB Wilfert, KR Chao, M Kaushal, S Jain, S Zöllner… - Nature …, 2016 - europepmc.org
Standard techniques from genetic epidemiology are ill-suited to formally assess the
significance of variants identified from a single case. We developed a statistical inference …
significance of variants identified from a single case. We developed a statistical inference …