WILLIAM CRAIGEN to High-Throughput Nucleotide Sequencing
This is a "connection" page, showing publications WILLIAM CRAIGEN has written about High-Throughput Nucleotide Sequencing.
Connection Strength
0.212
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Detection and Quantification of Mosaic Mutations in Disease Genes by Next-Generation Sequencing. J Mol Diagn. 2016 05; 18(3):446-453.
Score: 0.087
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Clinical application of massively parallel sequencing in the molecular diagnosis of glycogen storage diseases of genetically heterogeneous origin. Genet Med. 2013 Feb; 15(2):106-14.
Score: 0.068
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Assessment of genes involved in lysosomal diseases using the ClinGen clinical validity framework. Mol Genet Metab. 2024 Nov; 143(3):108593.
Score: 0.040
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Transition to next generation analysis of the whole mitochondrial genome: a summary of molecular defects. Hum Mutat. 2013 Jun; 34(6):882-93.
Score: 0.018