High-throughput sequencing approaches for diagnosing hereditary bleeding and platelet disorders

Keyphrases

• Platelet Dysfunction 100%
• Sequence Method 100%
• High-throughput Sequencing 100%
• Hereditary Bleeding Disorders 100%
• Bleeding Disorders 66%
• Diagnostic Performance 33%
• Bleeding 33%
• Etiology 16%
• Exon 16%
• Targeted Sequencing 16%
• Genetic Heterogeneity 16%
• Platelet Function 16%
• Clinical Symptoms 16%
• Unknown Etiology 16%
• Novel Genes 16%
• Whole Genome Sequencing 16%
• Mode of Inheritance 16%
• Pathogenic Variants 16%
• Regulatory Landscape 16%
• Megakaryopoiesis 16%
• Blood System 16%
• Looming 16%
• Diagnostic Practices 16%
• Platelet Formation 16%
• Digenic Inheritance 16%

Medicine and Dentistry

• Platelet Disorder 100%
• Bleeding Disorder 100%
• Diagnosis 50%
• Bleeding 33%
• Disease 16%
• Thrombocyte Function 16%
• Whole Genome Sequencing 16%
• Exon 16%
• Genetic Heterogeneity 16%
• Thrombocytopoiesis 16%
• Megakaryopoiesis 16%

Biochemistry, Genetics and Molecular Biology

• High Throughput Sequencing 100%
• Platelet 100%
• Exon 16%
• Whole Genome Sequencing 16%
• Genetic Heterogeneity 16%
• Thrombocyte Function 16%
• Thrombopoiesis 16%
• Megakaryocytopoiesis 16%