(Q42696451)

English

mit-o-matic: a comprehensive computational pipeline for clinical evaluation of mitochondrial variations from next-generation sequencing datasets

scientific article published on April 2015

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scholarly article

1 reference

Europe PubMed Central

5 November 2017

mit-o-matic: a comprehensive computational pipeline for clinical evaluation of mitochondrial variations from next-generation sequencing datasets (English)

1 reference

Europe PubMed Central

5 November 2017

1 reference

based on heuristic

inferred from title

6

1 reference

Europe PubMed Central

5 November 2017

author name string

Shamsudheen Karuthedath Vellarikkal

1

1 reference

Europe PubMed Central

5 November 2017

Heena Dhiman

2

1 reference

Europe PubMed Central

5 November 2017

Kandarp Joshi

3

1 reference

Europe PubMed Central

5 November 2017

Yasha Hasija

4

1 reference

Europe PubMed Central

5 November 2017

Sridhar Sivasubbu

5

1 reference

Europe PubMed Central

5 November 2017

publication date

1 April 2015

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Europe PubMed Central

5 November 2017

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Europe PubMed Central

5 November 2017

36

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Europe PubMed Central

5 November 2017

4

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Europe PubMed Central

5 November 2017

419-424

1 reference

Europe PubMed Central

5 November 2017

Mitochondrial mutations in patients with congenital heart defects by next generation sequencing technology.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22767

21 January 2018

Evolution of mitochondrial gene content: gene loss and transfer to the nucleus

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22767

21 January 2018

Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22767

21 January 2018

MToolBox: a highly automated pipeline for heteroplasmy annotation and prioritization analysis of human mitochondrial variants in high-throughput sequencing

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22767

21 January 2018

Exome sequencing of a patient with suspected mitochondrial disease reveals a likely multigenic etiology.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22767

21 January 2018

Comprehensive next-generation sequence analyses of the entire mitochondrial genome reveal new insights into the molecular diagnosis of mitochondrial DNA disorders

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22767

21 January 2018

The development of next-generation sequencing assays for the mitochondrial genome and 108 nuclear genes associated with mitochondrial disorders

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22767

21 January 2018

An update to MitoTool: using a new scoring system for faster mtDNA haplogroup determination.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22767

21 January 2018

Dynamics of mitochondrial heteroplasmy in three families investigated via a repeatable re-sequencing study

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22767

21 January 2018

MitoSeek: extracting mitochondria information and performing high-throughput mitochondria sequencing analysis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22767

21 January 2018

Heteroplasmic mitochondrial DNA mutations in normal and tumour cells

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22767

21 January 2018

Next generation sequencing to characterize mitochondrial genomic DNA heteroplasmy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22767

21 January 2018

ART: a next-generation sequencing read simulator.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22767

21 January 2018

mtDB: Human Mitochondrial Genome Database, a resource for population genetics and medical sciences

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22767

21 January 2018

MitoLSDB: a comprehensive resource to study genotype to phenotype correlations in human mitochondrial DNA variations

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22767

21 January 2018

Mitochondrial DNA mutations in pancreatic cancer

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22767

21 January 2018

MITOMAP: a human mitochondrial genome database

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22767

21 January 2018

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22767

21 January 2018

The preprotein translocation channel of the outer membrane of mitochondria.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22767

21 January 2018

Ultrafast and memory-efficient alignment of short DNA sequences to the human genome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22767

21 January 2018

Mitochondrial nuclear receptors and transcription factors: who's minding the cell?

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22767

21 January 2018

Fast and accurate short read alignment with Burrows-Wheeler transform

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22767

21 January 2018

Mapping short DNA sequencing reads and calling variants using mapping quality scores

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22767

21 January 2018

Detecting heteroplasmy from high-throughput sequencing of complete human mitochondrial DNA genomes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22767

21 January 2018

The Human MitoChip: a high-throughput sequencing microarray for mitochondrial mutation detection.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22767

21 January 2018

A disulfide relay system in the intermembrane space of mitochondria that mediates protein import

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22767

21 January 2018

Mitochondrial protein import: from proteomics to functional mechanisms

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22767

21 January 2018

Detection of ultra-rare mutations by next-generation sequencing

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22767

21 January 2018

Expression and maintenance of mitochondrial DNA: new insights into human disease pathology

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22767

21 January 2018

Minimum birth prevalence of mitochondrial respiratory chain disorders in children.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22767

21 January 2018

Neutral mitochondrial heteroplasmy and the influence of aging

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22767

21 January 2018

Next-generation sequencing of human mitochondrial reference genomes uncovers high heteroplasmy frequency

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22767

21 January 2018

Mitochondrial DNA mutations in human disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22767

21 January 2018

Use of y chromosome and mitochondrial DNA population structure in tracing human migrations

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22767

21 January 2018

Machinery for protein sorting and assembly in the mitochondrial outer membrane

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22767

21 January 2018

Mitochondrial defects and oxidative stress in Alzheimer disease and Parkinson disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22767

21 January 2018

Opening the door to mitochondrial protein import

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22767

7 January 2021

based on heuristic

inferred from DOI database lookup

Mitochondrial DNA portrait of Latvians: towards the understanding of the genetic structure of Baltic-speaking populations

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22767

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/HUMU.22767

1 reference

Europe PubMed Central

5 November 2017

1 reference

Europe PubMed Central

5 November 2017

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