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Publications by Pubudu Saneth Samarakoon
cnvScan: A CNV Screening and Annotation Tool to Improve the Clinical Utility of Computational CNV Prediction From Exome Sequencing Data
BMC Genomics
Biotechnology
Genetics
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Clinical Exome Sequencing as the First-Tier Test for Diagnosing Developmental Disorders Covering Both CNV and SNV: A Chinese Cohort
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First Genome-Wide CNV Mapping in FELIS CATUS Using Next Generation Sequencing Data
BMC Genomics
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CNVassoc: Association Analysis of CNV Data Using R
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Prediction and Prioritization of Neoantigens: Integration of RNA Sequencing Data With Whole-Exome Sequencing
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Correction: Identifying Human Genome-Wide CNV, LOH and UPD by Targeted Sequencing of Selected Regions
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Integrated Analysis of SNP, CNV and Gene Expression Data in Genetic Association Studies
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Digital Droplet PCR: CNV Analysis and Other Applications
Current Protocols in Human Genetics
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Contingent Negative Variation (CNV) and Lexical Decision Task
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CNV (Contingent Negative Variation) in Neurosurgical Patients
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