AluMine: alignment-free method for the discovery of polymorphic Alu element insertions
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Title
AluMine: alignment-free method for the discovery of polymorphic Alu element insertions
Authors
Keywords
Alu repeat element, Mobile element insertions, Alignment-free sequence analysis
Journal
Mobile DNA
Volume 10, Issue 1, Pages -
Publisher
Springer Science and Business Media LLC
Online
2019-07-18
DOI
10.1186/s13100-019-0174-3
References
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Note: Only part of the references are listed.- Primer3_masker: integrating masking of template sequence with primer design software
- (2018) Triinu Kõressaar et al. BIOINFORMATICS
- OUP accepted manuscript
- (2018) DNA RESEARCH
- Improved imputation accuracy of rare and low-frequency variants using population-specific high-coverage WGS-based imputation reference panel
- (2017) Mario Mitt et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Mobile DNA in Health and Disease
- (2017) Haig H. Kazazian et al. NEW ENGLAND JOURNAL OF MEDICINE
- Structural variants caused byAluinsertions are associated with risks for many human diseases
- (2017) Lindsay M. Payer et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- ALU ternative Regulation for Gene Expression
- (2017) Ling-Ling Chen et al. TRENDS IN CELL BIOLOGY
- FastGT: an alignment-free method for calling common SNVs directly from raw sequencing reads
- (2017) Fanny-Dhelia Pajuste et al. Scientific Reports
- Population-wide sampling of retrotransposon insertion polymorphisms using deep sequencing and efficient detection
- (2017) Qichao Yu et al. GigaScience
- Retrotransposons as regulators of gene expression
- (2016) R. A. Elbarbary et al. SCIENCE
- Identification of human-specific AluS elements through comparative genomics
- (2015) Jae Lee et al. GENE
- An integrated map of structural variation in 2,504 human genomes
- (2015) Peter H. Sudmant et al. NATURE
- The Dfam database of repetitive DNA families
- (2015) Robert Hubley et al. NUCLEIC ACIDS RESEARCH
- Tangram: a comprehensive toolbox for mobile element insertion detection
- (2014) Jiantao Wu et al. BMC GENOMICS
- T-lex2: genotyping, frequency estimation and re-annotation of transposable elements using single or pooled next-generation sequencing data
- (2014) Anna-Sophie Fiston-Lavier et al. NUCLEIC ACIDS RESEARCH
- Mobile element scanning (ME-Scan) identifies thousands of novel Alu insertions in diverse human populations
- (2013) D. J. Witherspoon et al. GENOME RESEARCH
- Detecting Alu insertions from high-throughput sequencing data
- (2013) Matei David et al. NUCLEIC ACIDS RESEARCH
- RetroSeq: transposable element discovery from next-generation sequencing data
- (2012) Thomas M. Keane et al. BIOINFORMATICS
- SINE Retrotransposons Cause Epigenetic Reprogramming of Adjacent Gene Promoters
- (2012) M. R. H. Estecio et al. MOLECULAR CANCER RESEARCH
- Dfam: a database of repetitive DNA based on profile hidden Markov models
- (2012) Travis J. Wheeler et al. NUCLEIC ACIDS RESEARCH
- Primer3—new capabilities and interfaces
- (2012) Andreas Untergasser et al. NUCLEIC ACIDS RESEARCH
- Landscape of Somatic Retrotransposition in Human Cancers
- (2012) E. Lee et al. SCIENCE
- Mobile elements in the human genome: implications for disease
- (2012) Szilvia Solyom et al. Genome Medicine
- Novel polymorphic AluYb8 insertion in the WNK1 gene is associated with blood pressure variation in Europeans
- (2011) Margus Putku et al. HUMAN MUTATION
- A Comprehensive Map of Mobile Element Insertion Polymorphisms in Humans
- (2011) Chip Stewart et al. PLoS Genetics
- Repetitive Elements May Comprise Over Two-Thirds of the Human Genome
- (2011) A. P. Jason de Koning et al. PLoS Genetics
- Next-generation VariationHunter: combinatorial algorithms for transposon insertion discovery
- (2010) Fereydoun Hormozdiari et al. BIOINFORMATICS
- Alu repeat discovery and characterization within human genomes
- (2010) F. Hormozdiari et al. GENOME RESEARCH
- Genome-wide mapping and assembly of structural variant breakpoints in the mouse genome
- (2010) A. R. Quinlan et al. GENOME RESEARCH
- The Sequence Alignment/Map format and SAMtools
- (2009) H. Li et al. BIOINFORMATICS
- Mobile elements create structural variation: Analysis of a complete human genome
- (2009) J. Xing et al. GENOME RESEARCH
- BioVenn – a web application for the comparison and visualization of biological lists using area-proportional Venn diagrams
- (2008) Tim Hulsen et al. BMC GENOMICS
- Mammalian non-LTR retrotransposons: For better or worse, in sickness and in health
- (2008) V. P. Belancio et al. GENOME RESEARCH
- Active Alu retrotransposons in the human genome
- (2008) E. A. Bennett et al. GENOME RESEARCH
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