Analytical Validation of an Early Detection Pancreatic Cancer Test Using 5-Hydroxymethylation Signatures

2024-9-1

Table of Contents

2024-9-1

Validation and Implementation of a Somatic-Only Tumor Exome for Routine Clinical Application

2024-9-1

Comparison of Results from Two Commercially Available In-house Tissue-Based Comprehensive Genomic Profiling Solutions: Research Use Only AVENIO Tumor Tissue CGP (AVENIO CGP) Kit and TruSight Oncology 500 (TSO-500) Assay

2024-9-1

Improved genetic characterization of congenital adrenal hyperplasia by long-read sequencing compared with multiplex ligation-dependent probe amplification plus Sanger sequencing

2024-9-1

Haplotype-aware detection of SERPINA1 variants by nanopore sequencing

2024-9-1

Editorial Board

2024-8-23

TPMT∗8

2024-8-1

Implementation of a High-Accuracy Targeted Gene Expression Panel for Clinical Care

2024-8-1

The correlation between plasma circulating tumor DNA and radiographic tumor burden

2024-8-1

Table of Contents

2024-8-1

Economic Impact of Whole Genome Sequencing and Whole Transcriptome Sequencing Versus Routine Diagnostic Molecular Testing to Stratify Patients with B-Cell Acute Lymphoblastic Leukemia

2024-8-1

Editorial Board

2024-8-1

Performance Characteristics of NGS-Based Engraftment Monitoring and Microchimerism Detection in Allogeneic Hematopoietic Cell Transplantation: A Practical Approach for Clinical Assay Validation

2024-8-1

PurIST Pancreatic Cancer Classifier: Analytic Validation of a 16-RNA Expression Signature Distinguishing Basal and Classical Subtypes

2024-8-1

Tailored Digital PCR Follow-Up of Rare Fusion Transcripts after Initial Detection through RNA Sequencing in Hematological Malignancies

2024-8-1

Analytical Validation of the Multitarget Stool RNA Test for Colorectal Cancer Screening

2024-7-10

Assessing the risk stratification of breast cancer polygenic risk scores in a Brazilian cohort

2024-7-1

Development, Validation, and Implementation of an Augmented Multiwell, Multitarget Quantitative PCR for the Analysis of Human Papillomavirus Genotyping through Software Automation, Data Science, and Artificial Intelligence

2024-7-1

The Utility of Real-time PCR, Metagenomic Next-generation Sequencing, and Culture in Bronchoalveolar Lavage Fluid for Diagnosis of Pulmonary Aspergillosis

2024-7-1

Clinical Validation of a Targeted Next-Generation Sequencing Panel for Lymphoid Malignancies

2024-7-1

Table of Contents

2024-7-1

Optimization of tumor dissection procedures leads to measurable improvement in the quality of molecular testing

2024-7-1

Strategic Implementation of Fragile X Carrier Screening in China: A Focused Pilot Study

2024-7-1

Characterization of Reference Materials for DPYD: A GeT-RM Collaborative Project

2024-7-1

Multisite Evaluation and Validation of Optical Genome Mapping for Prenatal Genetic Testing

2024-7-1

Comparative Analysis of Gene Expression Analysis Methods for RNA in Situ Hybridization Images

2024-7-1

A network-based framework to discover treatment-response-predicting biomarkers for complex diseases

2024-7-1

Genotype and Phenotype Correlation of Patients with Osteogenesis Imperfecta

2024-7-1

CRISPR-Based Assays for Point-of-Need Detection and Subtyping of Influenza

2024-7-1

Editorial Board

2024-7-1

DPYD Genotyping Recommendations: A Joint Consensus Recommendation of the Association for Molecular Pathology, American College of Medical Genetics and Genomics, Clinical Pharmacogenetics Implementation Consortium, College of American Pathologists, Dutch Pharmacogenetics Working Group of the Royal Dutch Pharmacists Association, European Society for Pharmacogenomics and Personalized Therapy, Pharmacogenomics Knowledgebase, and Pharmacogene Variation Consortium

2024-7-1

Mono- and biallelic replication-coupled gene editing discriminates dominant-negative and loss-of-function variants of DNA mismatch repair genes

2024-6-24

Accuracy of cobas MTB and MTB-RIF/INH for Detection of Mycobacterium tuberculosis and Drug Resistance

2024-6-7

Open-Source Bioinformatic Pipeline to Improve PMS2 Genetic Testing Using Short-Read NGS Data

2024-6-7

Performance Evaluation of a Commercial Automated Library Preparation System for Clinical Microbial Whole-Genome Sequencing Assays

2024-6-6

Recommendations for Tumor Mutational Burden Assay Validation and Reporting: A Joint Consensus Recommendation of the Association for Molecular Pathology, College of American Pathologists, and Society for Immunotherapy of Cancer

2024-6-6

Colorectal Cancer Screening: Increasing the Options

2024-6-6

Author Index

2024-6-1

Abstracts of the AMP Europe 2024 Congress

2024-6-1

Variant Detection in 3’ Exons of PMS2 Using Exome Sequencing Data

2024-6-1

Plasma protein profiling to discern indolent from advanced systemic mastocytosis

2024-6-1

Table of Contents

2024-6-1

Advances in host depletion and pathogen enrichment methods for rapid sequencing-based diagnosis of bloodstream infection

2024-6-1

Correction

2024-6-1

Editorial Board

2024-5-16

Table of Contents

2024-5-1

Correction

2024-5-1

Panel Comparative Analysis Tool

2024-5-1

EarlyTect BCD, a Streamlined PENK Methylation Test in Urine DNA, Effectively Detects Bladder Cancer in Patients with Hematuria

2024-4-25