Abstract Motivation: The increasing availability of mitochondria-targeted and off-target sequencing data in whole-exome and whole-genome sequencing studies (WXS and WGS) has risen the demand of effective pipelines to accurately measure heteroplasmy and to easily recognize the most functionally important mitochondrial variants among a huge number of candidates. To this purpose, we developed MToolBox, a highly automated pipeline to reconstruct and analyze human mitochondrial DNA from high-throughput sequencing data. Results: MToolBox implements an effective computational strategy for mitochondrial genomes assembling and haplogroup assignment also including a prioritization analysis of detected variants. MToolBox provides a Variant Call ...
Abstract Background Mitochondrial dysfunction is linked to numerous pathological states, in particul...
Background Whole Exome Sequencing (WES) is one of the most used and cost-effective next generatio...
Heteroplasmy, the existence of multiple mtDNA types within an individual, has been previously detect...
Motivation: The increasing availability of mitochondria-targeted and off-target sequencing data in w...
Motivation: The increasing availability of mitochondria-targeted and off-targeted sequencing data in...
MToolBox: a highly automated pipeline for heteroplasmy annota-tion and prioritization analysis of hu...
Abstract Background Whole genome and exome sequencing usually include reads containing mitochondrial...
Background Mitochondrial genome sequence analysis is critical to the diagnostic evaluation of mitoch...
Mitochondrial diseases are a heterogeneous group of disorders that can be caused by mutations in the...
Assigning a pathogenic role to mitochondrial DNA (mtDNA) variants and unveiling the potential involv...
International audienceBACKGROUND: Mitochondrial genome sequence analysis is critical to the diagnost...
We describe methods for rapid sequencing of the entire human mitochondrial genome (mtgenome), which ...
<div><p>We describe methods for rapid sequencing of the entire human mitochondrial genome (mtgenome)...
The growing number of next-generation sequencing (NGS) data presents a unique opportunity to study t...
International audienceThe development of next generation sequencing (NGS) has greatly enhanced the d...
Abstract Background Mitochondrial dysfunction is linked to numerous pathological states, in particul...
Background Whole Exome Sequencing (WES) is one of the most used and cost-effective next generatio...
Heteroplasmy, the existence of multiple mtDNA types within an individual, has been previously detect...
Motivation: The increasing availability of mitochondria-targeted and off-target sequencing data in w...
Motivation: The increasing availability of mitochondria-targeted and off-targeted sequencing data in...
MToolBox: a highly automated pipeline for heteroplasmy annota-tion and prioritization analysis of hu...
Abstract Background Whole genome and exome sequencing usually include reads containing mitochondrial...
Background Mitochondrial genome sequence analysis is critical to the diagnostic evaluation of mitoch...
Mitochondrial diseases are a heterogeneous group of disorders that can be caused by mutations in the...
Assigning a pathogenic role to mitochondrial DNA (mtDNA) variants and unveiling the potential involv...
International audienceBACKGROUND: Mitochondrial genome sequence analysis is critical to the diagnost...
We describe methods for rapid sequencing of the entire human mitochondrial genome (mtgenome), which ...
<div><p>We describe methods for rapid sequencing of the entire human mitochondrial genome (mtgenome)...
The growing number of next-generation sequencing (NGS) data presents a unique opportunity to study t...
International audienceThe development of next generation sequencing (NGS) has greatly enhanced the d...
Abstract Background Mitochondrial dysfunction is linked to numerous pathological states, in particul...
Background Whole Exome Sequencing (WES) is one of the most used and cost-effective next generatio...
Heteroplasmy, the existence of multiple mtDNA types within an individual, has been previously detect...