Review
Published on 16 Aug 2023
Resolving complex structural variants via nanopore sequencing
in Cancer Genetics and Oncogenomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1213917
- 11,857 views
- 17 citations
24 articles related to "Structural Variants Svs"
Articles
Brief Research Report
Published on 25 Aug 2022
Exonization of a deep intronic long interspersed nuclear element in Becker muscular dystrophy
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2022.979732
- 2,715 views
- 5 citations
Original Research
Published on 04 Jan 2023
Ten new high-quality genome assemblies for diverse bioenergy sorghum genotypes
in Plant Bioinformatics
Frontiers in Plant Science
doi 10.3389/fpls.2022.1040909
- 4,391 views
- 9 citations
Original Research
Published on 25 Mar 2022
Beta-Amylase and Phosphatidic Acid Involved in Recalcitrant Seed Germination of Chinese Chestnut
in Plant Bioinformatics
Frontiers in Plant Science
doi 10.3389/fpls.2022.828270
- 4,123 views
- 3 citations
Review
Published on 18 Feb 2014
The challenges and importance of structural variation detection in livestock
in Evolutionary and Population Genetics
Frontiers in Genetics
doi 10.3389/fgene.2014.00037
- 18,509 views
- 114 citations
Brief Research Report
Published on 18 Nov 2021
Evaluation of Germline Structural Variant Calling Methods for Nanopore Sequencing Data
in Computational Genomics
Frontiers in Genetics
doi 10.3389/fgene.2021.761791
- 11,110 views
- 21 citations
Review
Published on 29 Nov 2022
Recent advances and current challenges in population genomics of structural variation in animals and plants
in Evolutionary and Population Genetics
Frontiers in Genetics
doi 10.3389/fgene.2022.1060898
- 8,979 views
- 19 citations
Original Research
Published on 20 Oct 2022
Comprehensive analysis of structural variants in chickens using PacBio sequencing
in Livestock Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.971588
- 5,416 views
- 10 citations
Original Research
Published on 09 Jul 2024
HapKled: a haplotype-aware structural variant calling approach for Oxford nanopore sequencing data
in Computational Genomics
Frontiers in Genetics
doi 10.3389/fgene.2024.1435087
- 2,184 views
Original Research
Published on 10 May 2023
Characterization of pharmacogenomic variants in a Brazilian admixed cohort of elderly individuals based on whole-genome sequencing data
in Pharmacogenetics and Pharmacogenomics
Frontiers in Pharmacology
doi 10.3389/fphar.2023.1178715
- 4,298 views
- 9 citations
Original Research
Published on 24 Jul 2023
Whole genome sequencing for metastatic mutational burden in extraskeletal myxoid chondrosarcoma
in Molecular Medicine and Cancer Treatment
Frontiers in Molecular Medicine
doi 10.3389/fmmed.2023.1152550
- 4,004 views
- 1 citation
Technology and Code
Published on 01 Dec 2021
SVInterpreter: A Comprehensive Topologically Associated Domain-Based Clinical Outcome Prediction Tool for Balanced and Unbalanced Structural Variants
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2021.757170
- 5,091 views
- 6 citations
Original Research
Published on 04 Feb 2021
Analysis of Structural Variants Reveal Novel Selective Regions in the Genome of Meishan Pigs by Whole Genome Sequencing
in Evolutionary and Population Genetics
Frontiers in Genetics
doi 10.3389/fgene.2021.550676
- 7,412 views
- 21 citations
Methods
Published on 05 May 2022
kngMap: Sensitive and Fast Mapping Algorithm for Noisy Long Reads Based on the K-Mer Neighborhood Graph
in Computational Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.890651
- 4,316 views
- 8 citations
Original Research
Published on 18 May 2023
Genome sequencing with comprehensive variant calling identifies structural variants and repeat expansions in a large fraction of individuals with ataxia and/or neuromuscular disorders
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2023.1170005
- 6,206 views
- 7 citations
Original Research
Published on 14 Jan 2020
Location of Balanced Chromosome-Translocation Breakpoints by Long-Read Sequencing on the Oxford Nanopore Platform
in Genomic Assay Technology
Frontiers in Genetics
doi 10.3389/fgene.2019.01313
- 21,786 views
- 55 citations