NUMT Confounding Biases Mitochondrial Heteroplasmy Calls in Favor of the Reference Allele
Published 2019 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
NUMT Confounding Biases Mitochondrial Heteroplasmy Calls in Favor of the Reference Allele
Authors
Keywords
-
Journal
Frontiers in Cell and Developmental Biology
Volume 7, Issue -, Pages -
Publisher
Frontiers Media SA
Online
2019-09-25
DOI
10.3389/fcell.2019.00201
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Novel and heteroplasmic mutations in mitochondrial tRNA genes in Brugada syndrome
- (2018) Mahsasadat Fallah Tafti et al. Cardiology Journal
- Recent Advances in Detecting Mitochondrial DNA Heteroplasmic Variations
- (2018) et al. MOLECULES
- Sensitive detection of mitochondrial DNA variants for analysis of mitochondrial DNA-enriched extracts from frozen tumor tissue
- (2018) M. J. A. Weerts et al. Scientific Reports
- Assessing mitochondrial heteroplasmy using next generation sequencing: A note of caution
- (2018) Mauro Santibanez-Koref et al. MITOCHONDRION
- The ability of human nuclear DNA to cause false positive low-abundance heteroplasmy calls varies across the mitochondrial genome
- (2016) Levent Albayrak et al. BMC GENOMICS
- The dynamics of mitochondrial DNA heteroplasmy: implications for human health and disease
- (2015) James B. Stewart et al. NATURE REVIEWS GENETICS
- Assessing Mitochondrial DNA Variation and Copy Number in Lymphocytes of ~2,000 Sardinians Using Tailored Sequencing Analysis Tools
- (2015) Jun Ding et al. PLoS Genetics
- Two novel mutations in COII and tRNAHis mitochondrial genes in asthenozoospermic infertiles men
- (2014) Baklouti-Gargouri Siwar et al. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
- Isaac: ultra-fast whole-genome secondary analysis on Illumina sequencing platforms
- (2013) Come Raczy et al. BIOINFORMATICS
- Functional Recurrent Mutations in the Human Mitochondrial Phylogeny: Dual Roles in Evolution and Disease
- (2013) Liron Levin et al. Genome Biology and Evolution
- The case for the continuing use of the revised Cambridge Reference Sequence (rCRS) and the standardization of notation in human mitochondrial DNA studies
- (2013) Hans-Jürgen Bandelt et al. JOURNAL OF HUMAN GENETICS
- Fidelity of capture-enrichment for mtDNA genome sequencing: influence of NUMTs
- (2012) Mingkun Li et al. NUCLEIC ACIDS RESEARCH
- The reference human nuclear mitochondrial sequences compilation validated and implemented on the UCSC genome browser
- (2011) Domenico Simone et al. BMC GENOMICS
- Nuclear insertions of mitochondrial origin: Database updating and usefulness in cancer studies
- (2011) Amanda Ramos et al. MITOCHONDRION
- A framework for variation discovery and genotyping using next-generation DNA sequencing data
- (2011) Mark A DePristo et al. NATURE GENETICS
- SNPedia: a wiki supporting personal genome annotation, interpretation and analysis
- (2011) Michael Cariaso et al. NUCLEIC ACIDS RESEARCH
- Genetic variants in mitochondrial tRNA genes are associated with essential hypertension in a Chinese Han population
- (2009) Hai-Yan Zhu et al. CLINICA CHIMICA ACTA
- Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation
- (2009) Jianxin Lu et al. MITOCHONDRION
- Updated comprehensive phylogenetic tree of global human mitochondrial DNA variation
- (2008) Mannis van Oven et al. HUMAN MUTATION
Publish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn MoreFind the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
Search