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Publications by David R FitzPatrick
Variant Detection Sensitivity and Biases in Whole Genome and Exome Sequencing
BMC Bioinformatics
Biochemistry
Applied Mathematics
Computer Science Applications
Structural Biology
Molecular Biology
Related publications
Whole-Genome Sequencing Is More Powerful Than Whole-Exome Sequencing for Detecting Exome Variants
Proceedings of the National Academy of Sciences of the United States of America
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Whole-Genome Sequencing and Disease-Gene Detection
BMC Proceedings
Biochemistry
Medicine
Genetics
Molecular Biology
THU0005 Whole Genome Linkage and Exome Sequencing Analyses in Takayasu Arteritis Families
Whole Genome Sequencing and Rare Variant Analysis in Essential Tremor Families
PLoS ONE
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Clinical Cancer Genomic Profiling by Three-Platform Sequencing of Whole Genome, Whole Exome and Transcriptome
Nature Communications
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Molecular Biology
Biochemistry
Chemistry
Physics
Whole Exome Sequencing and the Clinician: We Need Clinical Skills and Functional Validation in Variant Filtering
Journal of Neurology
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Whole Exome Sequencing in Monogenic Dyslipidemias
Journal of Atherosclerosis and Thrombosis
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Impact of DNA Source on Genetic Variant Detection From Human Whole-Genome Sequencing Data
Journal of Medical Genetics
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Comparison of Three Variant Callers for Human Whole Genome Sequencing
Scientific Reports
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