Table 1.
Subject Area* | Specific Topic | Percentage Responding (Excellent/Very Good) | Mean**+ |
---|---|---|---|
Molecular pathology | Polymerase Chain Reaction (PCR) | 25% | 2.85 |
DNA Sequencing | 18% | 2.60 | |
Combined topics | Single nucleotide polymorphism (SNP) | 11% | 2.25 |
Microarray data | 11% | 2.24 | |
Genomic medicine | Next- generation sequencing (NGS) | 9% | 2.08 |
Genome- wide association studies (GWAS) | 6% | 1.94 |
Specific topics grouped into three subject areas by authors
Examinees were asked to rate their “ability to determine the clinical significance” of data related to each specific topic. Response options: (1) Poor, (2)Fair, (3)Good, (4)Very Good, (5)Excellent
P <0.001 (one-way ANOVA comparing topic areas)