Concordance between Research Sequencing and Clinical Pharmacogenetic Genotyping in the eMERGE-PGx Study.

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Institutional profile: translational pharmacogenomics at the Icahn School of Medicine at Mount Sinai.Identification and characterization of TP53 gene Allele Dropout in Li-Fraumeni syndrome and Oral cancer cohorts

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Concordance between Research Sequencing and Clinical Pharmacogenetic Genotyping in the eMERGE-PGx Study.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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Concordance between Research S ...... yping in the eMERGE-PGx Study.

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Concordance between Research S ...... yping in the eMERGE-PGx Study.

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Concordance between Research S ...... yping in the eMERGE-PGx Study.

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Concordance between Research S ...... yping in the eMERGE-PGx Study.

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Concordance between Research S ...... yping in the eMERGE-PGx Study.

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Concordance between Research S ...... yping in the eMERGE-PGx Study.

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Concordance between Research S ...... yping in the eMERGE-PGx Study.

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Adam S Gordon

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Ammar Husami

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Aniwaa Owusu Obeng

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Berta Almoguera

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Cynthia A Prows

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Hakon Hakonarson

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Iftikhar J Kullo

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Jared B Hawkins

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Kejian Zhang

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Kimberly F Doheny

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ClinVar: public archive of interpretations of clinically relevant variants

The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future

ACMG clinical laboratory standards for next-generation sequencing.

Design and anticipated outcomes of the eMERGE-PGx project: a multicenter pilot for preemptive pharmacogenomics in electronic health record systems.

A maximum-likelihood method to correct for allelic dropout in microsatellite data with no replicate genotypes.

Ethical and practical guidelines for reporting genetic research results to study participants: updated guidelines from a National Heart, Lung, and Blood Institute working group

Quality standards and samples in genetic testing.

Systematic Evaluation of Sanger Validation of Next-Generation Sequencing Variants

PGRNseq: a targeted capture sequencing panel for pharmacogenetic research and implementation.

Identification of an intronic single nucleotide polymorphism leading to allele dropout during validation of a CDH1 sequencing assay: implications for designing polymerase chain reaction-based assays.

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561-566

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scholarly article

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10.1016/J.JMOLDX.2017.04.002

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Marylyn D. Ritchie

Teri Manolio

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2017-05-11T00:00:00Z

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Concordance between Research Sequencing and Clinical Pharmacogenetic Genotyping in the eMERGE-PGx Study.

about

P2860

P2860

Concordance between Research Sequencing and Clinical Pharmacogenetic Genotyping in the eMERGE-PGx Study.

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