| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A Model Information Management Plan for Molecular Pathology Sequence Data Using Standards
|
Campbell, Walter S.
|
|
2019
|
21 |
3 |
p. 408-417
|
artikel
|
| 2 |
Analytical Validation of Variants to Aid in Genotype-Guided Therapy for Oncology
|
Swart, Marelize
|
|
2019
|
21 |
3 |
p. 491-502
|
artikel
|
| 3 |
A New Fast Phasing Method Based On Haplotype Subtraction
|
Mocci, Evelina
|
|
2019
|
21 |
3 |
p. 427-436
|
artikel
|
| 4 |
Designing and Implementing NGS Tests for Inherited Disorders
|
Santani, Avni
|
|
2019
|
21 |
3 |
p. 369-374
|
artikel
|
| 5 |
Editorial Board
|
|
|
2019
|
21 |
3 |
p. A1-A2
|
artikel
|
| 6 |
Genetic Diagnostic Testing for Inherited Cardiomyopathies
|
Daoud, Hussein
|
|
2019
|
21 |
3 |
p. 437-448
|
artikel
|
| 7 |
Genomic Analysis of Circulating Tumor DNA Using a Melanoma-Specific UltraSEEK Oncogene Panel
|
Gray, Elin S.
|
|
2019
|
21 |
3 |
p. 418-426
|
artikel
|
| 8 |
Highly Multiplexed Fluorescence in Situ Hybridization for in Situ Genomics
|
Onozato, Maristela L.
|
|
2019
|
21 |
3 |
p. 390-407
|
artikel
|
| 9 |
Leveraging Human Microbiome Features to Diagnose and Stratify Children with Irritable Bowel Syndrome
|
Hollister, Emily B.
|
|
2019
|
21 |
3 |
p. 449-461
|
artikel
|
| 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
|
artikel
|
| 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
|
artikel
|
| 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
|
artikel
|
| 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
|
artikel
|
| 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
|
artikel
|
| 15 |
Structural Variation Detection by Proximity Ligation from Formalin-Fixed, Paraffin-Embedded Tumor Tissue
|
Troll, Christopher J.
|
|
2019
|
21 |
3 |
p. 375-383
|
artikel
|
| 16 |
Table of Contents
|
|
|
2019
|
21 |
3 |
p. A3-A4
|
artikel
|
| 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
|
artikel
|
| 18 |
VarGrouper
|
Schmidt, Ryan J.
|
|
2019
|
21 |
3 |
p. 384-389
|
artikel
|
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