Methods
Published on 06 Jul 2023
A novel scatterplot-based method to detect copy number variation (CNV)
in Computational Genomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1166972
- 4,546 views
- 2 citations
138 articles related to "Copy Number Variation Cnv"
Articles
Original Research
Published on 16 Nov 2017
Effects of EPSPS Copy Number Variation (CNV) and Glyphosate Application on the Aromatic and Branched Chain Amino Acid Synthesis Pathways in Amaranthus palmeri
in Agroecology
Frontiers in Plant Science
doi 10.3389/fpls.2017.01970
- 7,146 views
- 27 citations
Original Research
Published on 25 Oct 2013
Evaluation of calling algorithms for array-CGH
in Statistical Genetics and Methodology
Frontiers in Genetics
doi 10.3389/fgene.2013.00217
- 6,899 views
- 14 citations
Review
Published on 13 Apr 2015
Whole-genome CNV analysis: advances in computational approaches
in Computational Genomics
Frontiers in Genetics
doi 10.3389/fgene.2015.00138
- 59,509 views
- 174 citations
Case Report
Published on 30 Jan 2026
Case Report: Sengers syndrome caused by a novel 7.6 kb AGK deletion misdiagnosed as isolated congenital cataract
in Genetics of Common and Rare Diseases
Frontiers in Pediatrics
doi 10.3389/fped.2026.1714952
- 370 views
Case Report
Published on 16 Aug 2024
HNF1β, LHX1, and GGNBP2 deletion contributed to kidney and reproductive dysfunction in 17q12 deletion syndrome: evidence from a case report
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2024.1391804
- 2,697 views
- 2 citations
Original Research
Published on 19 Dec 2019
Copy Number Variation Pattern for Discriminating MACROD2 States of Colorectal Cancer Subtypes
in Computational Genomics
Frontiers in Bioengineering and Biotechnology
doi 10.3389/fbioe.2019.00407
- 9,969 views
- 20 citations
Original Research
Published on 21 Mar 2019
A 57 kB Genomic Deletion Causing CTNS Loss of Function Contributes to the CTNS Mutational Spectrum in the Middle East
in Pediatric Nephrology
Frontiers in Pediatrics
doi 10.3389/fped.2019.00089
- 6,045 views
- 8 citations
Original Research
Published on 23 Mar 2022
Development of Tumor Mutation Burden-Related Prognostic Model and Novel Biomarker Identification in Stomach Adenocarcinoma
in Molecular and Cellular Oncology
Frontiers in Cell and Developmental Biology
doi 10.3389/fcell.2022.790920
- 5,102 views
- 13 citations
Original Research
Published on 26 Feb 2020
Predicting Stage-Specific Recurrent Aberrations From Somatic Copy Number Dataset
in Computational Genomics
Frontiers in Genetics
doi 10.3389/fgene.2020.00160
- 3,705 views
- 4 citations
Original Research
Published on 09 Feb 2018
Analysis of Extreme Phenotype Bulk Copy Number Variation (XP-CNV) Identified the Association of rp1 with Resistance to Goss's Wilt of Maize
in Technical Advances in Plant Science
Frontiers in Plant Science
doi 10.3389/fpls.2018.00110
- 8,002 views
- 27 citations
Original Research
Published on 04 Jul 2022
Differential Infiltration of Immune Cells Driven by Tumor Heterogeneity Reveals Two Immune Subtypes in Lung Adenocarcinoma
in Computational Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.924781
- 2,293 views
- 1 citation
Original Research
Published on 10 Nov 2021
Genetic Analysis of Children With Unexplained Developmental Delay and/or Intellectual Disability by Whole-Exome Sequencing
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2021.738561
- 8,856 views
- 28 citations
Original Research
Published on 04 Nov 2021
Copy Number Variation Identification on 3,800 Alzheimer’s Disease Whole Genome Sequencing Data from the Alzheimer’s Disease Sequencing Project
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2021.752390
- 5,594 views
- 13 citations
Case Report
Published on 22 Aug 2023
Case Report: Mycobacterium kansasii causing infective endocarditis explored by metagenomic next-generation sequencing
in Clinical and Diagnostic Microbiology and Immunology
Frontiers in Cellular and Infection Microbiology
doi 10.3389/fcimb.2023.1227537
- 3,267 views
- 6 citations
Perspective
Published on 04 Feb 2015
A genomic approach to study down syndrome and cancer inverse comorbidity: untangling the chromosome 21
in Systems Biology Archive
Frontiers in Physiology
doi 10.3389/fphys.2015.00010
- 10,727 views
- 20 citations