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A prospective assessment defining the limitations of thyroid nodule pathologic evaluation

Annals of internal medicine, 2013-09, Vol.159 (5), p.325

2013

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A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays

Cancer research (Chicago, Ill.), 2005-07, Vol.65 (14), p.6071-6079

2005

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Clinical validation and utility of Percepta GSC for the evaluation of lung cancer

PloS one, 2022-07, Vol.17 (7), p.e0268567-e0268567

2022

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Analytical and Clinical Validation of Expressed Variants and Fusions From the Whole Transcriptome of Thyroid FNA Samples

Frontiers in endocrinology (Lausanne), 2019-09, Vol.10, p.612-612

2019

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Identification of usual interstitial pneumonia pattern using RNA-Seq and machine learning: challenges and solutions

BMC genomics, 2018-05, Vol.19 (Suppl 2), p.101-101, Article 101

2018

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Analytical validation of the Percepta genomic sequencing classifier; an RNA next generation sequencing assay for the assessment of Lung Cancer risk of suspicious pulmonary nodules

BMC cancer, 2021-04, Vol.21 (1), p.400-400, Article 400

2021

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Percepta Genomic Sequencing Classifier and decision-making in patients with high-risk lung nodules: a decision impact study

BMC pulmonary medicine, 2022-01, Vol.22 (1), p.26-26, Article 26

2022

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Risk of malignancy in cytologically indeterminate thyroid nodules harboring thyroid stimulating hormone receptor mutations

Frontiers in endocrinology (Lausanne), 2022-12, Vol.13, p.1073592-1073592

2022

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Genome-wide surveillance of mismatched alleles for graft-versus-host disease in stem cell transplantation

Blood, 2015-12, Vol.126 (25), p.2752-2763

2015

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Improving lung cancer risk stratification leveraging whole transcriptome RNA sequencing and machine learning across multiple cohorts

BMC medical genomics, 2020-10, Vol.13 (Suppl 10), p.151-151, Article 151

2020

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Analytical Verification Performance of Afirma Genomic Sequencing Classifier in the Diagnosis of Cytologically Indeterminate Thyroid Nodules

Frontiers in endocrinology (Lausanne), 2019-07, Vol.10, p.438-438

2019

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Comparing modalities for risk assessment in patients with pulmonary lesions and nondiagnostic bronchoscopy for suspected lung cancer

BMC pulmonary medicine, 2022-11, Vol.22 (1), p.442-442, Article 442

2022

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Maximizing Small Biopsy Patient Samples: Unified RNA-Seq Platform Assessment of over 120,000 Patient Biopsies

Journal of personalized medicine, 2022-12, Vol.13 (1), p.24

2022

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Application of high-density DNA resequencing microarray for detection and characterization of botulinum neurotoxin-producing clostridia

PloS one, 2013-06, Vol.8 (6), p.e67510

2013

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Whole-Genome Scan, in a Complex Disease, Using 11,245 Single-Nucleotide Polymorphisms: Comparison with Microsatellites

American journal of human genetics, 2004-07, Vol.75 (1), p.54-64

2004

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Parallel genotyping of over 10,000 SNPs using a one-primer assay on a high-density oligonucleotide array

Genome research, 2004-03, Vol.14 (3), p.414

2004

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Analytical performance of Envisia: a genomic classifier for usual interstitial pneumonia

BMC pulmonary medicine, 2017-11, Vol.17 (1), p.141-141, Article 141

2017

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Preoperative Diagnosis of Benign Thyroid Nodules with Indeterminate Cytology

The New England journal of medicine, 2012-08, Vol.367 (8), p.705-715

2012

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The genomic distribution of population substructure in four populations using 8,525 autosomal SNPs

Human genomics, 2004-05, Vol.1 (4), p.274-286

2004

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High-Resolution Identification of Chromosomal Abnormalities Using Oligonucleotide Arrays Containing 116,204 SNPs

American journal of human genetics, 2005-11, Vol.77 (5), p.709-726

2005

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Utility of a Molecular Classifier as a Complement to High-Resolution Computed Tomography to Identify Usual Interstitial Pneumonia

American journal of respiratory and critical care medicine, 2021-01, Vol.203 (2), p.211-220

2021

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Mapping Human Genetic Diversity in Asia

Science (American Association for the Advancement of Science), 2009-12, Vol.326 (5959), p.1541-1545

2009

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An Oligonucleotide Microarray for High-Throughput Sequencing of the Mitochondrial Genome

The Journal of molecular diagnostics : JMD, 2006-09, Vol.8 (4), p.476-482

2006

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A prospective assessment defining the limitations of thyroid nodule pathologic evaluation

A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays

Clinical validation and utility of Percepta GSC for the evaluation of lung cancer

Classification of usual interstitial pneumonia in patients with interstitial lung disease: assessment of a machine learning approach using high-dimensional transcriptional data

Analytical and Clinical Validation of Expressed Variants and Fusions From the Whole Transcriptome of Thyroid FNA Samples

Identification of usual interstitial pneumonia pattern using RNA-Seq and machine learning: challenges and solutions

Analytical validation of the Percepta genomic sequencing classifier; an RNA next generation sequencing assay for the assessment of Lung Cancer risk of suspicious pulmonary nodules

Percepta Genomic Sequencing Classifier and decision-making in patients with high-risk lung nodules: a decision impact study

Risk of malignancy in cytologically indeterminate thyroid nodules harboring thyroid stimulating hormone receptor mutations

Genome-wide surveillance of mismatched alleles for graft-versus-host disease in stem cell transplantation

Improving lung cancer risk stratification leveraging whole transcriptome RNA sequencing and machine learning across multiple cohorts

Analytical Verification Performance of Afirma Genomic Sequencing Classifier in the Diagnosis of Cytologically Indeterminate Thyroid Nodules

Comparing modalities for risk assessment in patients with pulmonary lesions and nondiagnostic bronchoscopy for suspected lung cancer

Maximizing Small Biopsy Patient Samples: Unified RNA-Seq Platform Assessment of over 120,000 Patient Biopsies

Application of high-density DNA resequencing microarray for detection and characterization of botulinum neurotoxin-producing clostridia

Whole-Genome Scan, in a Complex Disease, Using 11,245 Single-Nucleotide Polymorphisms: Comparison with Microsatellites

Parallel genotyping of over 10,000 SNPs using a one-primer assay on a high-density oligonucleotide array

Analytical performance of Envisia: a genomic classifier for usual interstitial pneumonia

Performance of a Genomic Sequencing Classifier for the Preoperative Diagnosis of Cytologically Indeterminate Thyroid Nodules

Preoperative Diagnosis of Benign Thyroid Nodules with Indeterminate Cytology

The genomic distribution of population substructure in four populations using 8,525 autosomal SNPs

High-Resolution Identification of Chromosomal Abnormalities Using Oligonucleotide Arrays Containing 116,204 SNPs

Utility of a Molecular Classifier as a Complement to High-Resolution Computed Tomography to Identify Usual Interstitial Pneumonia

Mapping Human Genetic Diversity in Asia

An Oligonucleotide Microarray for High-Throughput Sequencing of the Mitochondrial Genome

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