Amanote Research

Amanote Research

    RegisterSign In

Discover open access scientific publications

Search, annotate, share and cite publications


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
BiotechnologyGenetics
2016English

Related publications

Clinical Exome Sequencing as the First-Tier Test for Diagnosing Developmental Disorders Covering Both CNV and SNV: A Chinese Cohort

Journal of Medical Genetics
Genetics
2020English

First Genome-Wide CNV Mapping in FELIS CATUS Using Next Generation Sequencing Data

BMC Genomics
BiotechnologyGenetics
2018English

CNVassoc: Association Analysis of CNV Data Using R

BMC Medical Genomics
Genetics
2011English

Prediction and Prioritization of Neoantigens: Integration of RNA Sequencing Data With Whole-Exome Sequencing

Cancer Science
Cancer ResearchMedicineOncology
2017English

Correction: Identifying Human Genome-Wide CNV, LOH and UPD by Targeted Sequencing of Selected Regions

PLoS ONE
Multidisciplinary
2015English

Integrated Analysis of SNP, CNV and Gene Expression Data in Genetic Association Studies

Clinical Genetics
Genetics
2017English

Digital Droplet PCR: CNV Analysis and Other Applications

Current Protocols in Human Genetics
MedicineGenetics
2014English

Contingent Negative Variation (CNV) and Lexical Decision Task

Shinrigaku Kenkyu
Psychology
1982English

CNV (Contingent Negative Variation) in Neurosurgical Patients

Neurologia Medico-Chirurgica
SurgeryNeurology
1981English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2026 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy