Detection of mutations in myeloid malignancies through paired-sample analysis of microdroplet-PCR deep sequencing data. [electronic resource]
Producer: 20151016Description: 504-518 p. digitalISSN:- 1943-7811
- Bone Marrow Cells -- metabolism
- DNA Mutational Analysis -- methods
- Exons
- Genetic Testing -- methods
- High-Throughput Nucleotide Sequencing -- methods
- Humans
- Leukemia, Myeloid -- diagnosis
- Mutation
- Myeloproliferative Disorders -- diagnosis
- Nucleophosmin
- Polymerase Chain Reaction -- methods
- Polymorphism, Single Nucleotide
- ROC Curve
- Reproducibility of Results
- Sensitivity and Specificity
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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