| no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
| 1 |
Adopting High-Resolution Allele Frequencies Substantially Expedites Variant Interpretation in Genetic Diagnostic Laboratories
|
Ghani, Mahdi
|
|
|
21 |
4 |
p. 602-611
|
article
|
| 2 |
Analytical Validation of a Highly Sensitive, Multiplexed Chronic Myeloid Leukemia Monitoring System Targeting BCR-ABL1 RNA
|
Brown, Justin T.
|
|
|
21 |
4 |
p. 718-733
|
article
|
| 3 |
An Effective Strategy to Eliminate Inherent Cross-Contamination in mtDNA Next-Generation Sequencing of Multiple Samples
|
Yin, Chun
|
|
|
21 |
4 |
p. 593-601
|
article
|
| 4 |
A Reference System for BRCA Mutation Detection Based on Next-Generation Sequencing in the Chinese Population
|
Qu, Shoufang
|
|
|
21 |
4 |
p. 677-686
|
article
|
| 5 |
Clinical Validation of a Cell-Free DNA Gene Panel
|
Cheng, Ju
|
|
|
21 |
4 |
p. 632-645
|
article
|
| 6 |
Considerations for Genomic Data Privacy and Security when Working in the Cloud
|
Carter, Alexis B.
|
|
|
21 |
4 |
p. 542-552
|
article
|
| 7 |
Detection of Single-Nucleotide Polymorphism Markers of Antimalarial Drug Resistance Directly from Whole Blood
|
Leelawong, Mindy
|
|
|
21 |
4 |
p. 623-631
|
article
|
| 8 |
Detection of Tumor NTRK Gene Fusions to Identify Patients Who May Benefit from Tyrosine Kinase (TRK) Inhibitor Therapy
|
Hsiao, Susan J.
|
|
|
21 |
4 |
p. 553-571
|
article
|
| 9 |
Development of a Novel Next-Generation Sequencing Assay for Carrier Screening in Old Order Amish and Mennonite Populations of Pennsylvania
|
Crowgey, Erin L.
|
|
|
21 |
4 |
p. 687-694
|
article
|
| 10 |
Editorial Board
|
|
|
|
21 |
4 |
p. A1-A2
|
article
|
| 11 |
Expanding the Scope of The Journal of Molecular Diagnostics to the Informatics Subdivision of the Association for Molecular Pathology
|
Carter, Alexis B.
|
|
|
21 |
4 |
p. 539-541
|
article
|
| 12 |
Fixation Effects on Variant Calling in a Clinical Resequencing Panel
|
Parker, Jeremy D.K.
|
|
|
21 |
4 |
p. 705-717
|
article
|
| 13 |
Multi-Gene Panel Testing of 23,179 Individuals for Hereditary Cancer Risk Identifies Pathogenic Variant Carriers Missed by Current Genetic Testing Guidelines
|
Neben, Cynthia L.
|
|
|
21 |
4 |
p. 646-657
|
article
|
| 14 |
Multilaboratory Assessment of a New Reference Material for Quality Assurance of Cell-Free Tumor DNA Measurements
|
He, Hua-Jun
|
|
|
21 |
4 |
p. 658-676
|
article
|
| 15 |
Multiplex Solid-Phase Melt Curve Analysis for the Point-of-Care Detection of HIV-1 Drug Resistance
|
Clutter, Dana S.
|
|
|
21 |
4 |
p. 580-592
|
article
|
| 16 |
Promoter Hypermethylation of Genes Encoding for RASSF/Hippo Pathway Members Reveals Specific Alteration Pattern in Diffuse Gliomas
|
Levallet, Guénaëlle
|
|
|
21 |
4 |
p. 695-704
|
article
|
| 17 |
Table of Contents
|
|
|
|
21 |
4 |
p. A3-A4
|
article
|
| 18 |
Tumor Heterogeneity Index to Detect Human Epidermal Growth Factor Receptor 2 Amplification by Next-Generation Sequencing
|
Choi, Sangjoon
|
|
|
21 |
4 |
p. 612-622
|
article
|
| 19 |
Validation of Extensive Next-Generation Sequencing Method for Monogenic Disorder Analysis on Cell-Free Fetal DNA
|
Dello Russo, Claudio
|
|
|
21 |
4 |
p. 572-579
|
article
|
Journal description