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                             18 results found
no title author magazine year volume issue page(s) type
1 A Model Information Management Plan for Molecular Pathology Sequence Data Using Standards Campbell, Walter S.
2019
21 3 p. 408-417
article
2 Analytical Validation of Variants to Aid in Genotype-Guided Therapy for Oncology Swart, Marelize
2019
21 3 p. 491-502
article
3 A New Fast Phasing Method Based On Haplotype Subtraction Mocci, Evelina
2019
21 3 p. 427-436
article
4 Designing and Implementing NGS Tests for Inherited Disorders Santani, Avni
2019
21 3 p. 369-374
article
5 Editorial Board 2019
21 3 p. A1-A2
article
6 Genetic Diagnostic Testing for Inherited Cardiomyopathies Daoud, Hussein
2019
21 3 p. 437-448
article
7 Genomic Analysis of Circulating Tumor DNA Using a Melanoma-Specific UltraSEEK Oncogene Panel Gray, Elin S.
2019
21 3 p. 418-426
article
8 Highly Multiplexed Fluorescence in Situ Hybridization for in Situ Genomics Onozato, Maristela L.
2019
21 3 p. 390-407
article
9 Leveraging Human Microbiome Features to Diagnose and Stratify Children with Irritable Bowel Syndrome Hollister, Emily B.
2019
21 3 p. 449-461
article
10 Optimization of Next-Generation Sequencing Technologies for von Hippel Lindau (VHL) Mosaic Mutation Detection and Development of Confirmation Methods Coppin, Lucie
2019
21 3 p. 462-470
article
11 Panel-Based Nuclear and Mitochondrial Next-Generation Sequencing Outcomes of an Ethnically Diverse Pediatric Patient Cohort with Mitochondrial Disease Schoonen, Maryke
2019
21 3 p. 503-513
article
12 Personalized Chimerism Test that Uses Selection of Short Tandem Repeat or Quantitative PCR Depending on Patient's Chimerism Status Tyler, Jennifer
2019
21 3 p. 483-490
article
13 Practical Bioinformatic DNA-Sequencing Pipeline for Detecting Oncogene Amplification and EGFRvIII Mutational Status in Clinical Glioblastoma Samples Miller, Michael L.
2019
21 3 p. 514-524
article
14 Rational “Error Elimination” Approach to Evaluating Molecular Barcoded Next-Generation Sequencing Data Identifies Low-Frequency Mutations in Hematologic Malignancies Mallampati, Saradhi
2019
21 3 p. 471-482
article
15 Structural Variation Detection by Proximity Ligation from Formalin-Fixed, Paraffin-Embedded Tumor Tissue Troll, Christopher J.
2019
21 3 p. 375-383
article
16 Table of Contents 2019
21 3 p. A3-A4
article
17 Validated Reference Panel from Renewable Source of Genomic DNA Available for Standardization of Blood Group Genotyping Volkova, Evgeniya
2019
21 3 p. 525-537
article
18 VarGrouper Schmidt, Ryan J.
2019
21 3 p. 384-389
article
                             18 results found
 
 Koninklijke Bibliotheek - National Library of the Netherlands