(Q27008228)

English

Mitochondrial Disease Sequence Data Resource (MSeqDR): a global grass-roots consortium to facilitate deposition, curation, annotation, and integrated analysis of genomic data for the mitochondrial disease clinical and research communities

scientific article (publication date: March 2015)

In more languages

Statements

scholarly article

0 references

1 reference

Europe PubMed Central

Mitochondrial Disease Sequence Data Resource (MSeqDR): a global grass-roots consortium to facilitate deposition, curation, annotation, and integrated analysis of genomic data for the mitochondrial disease clinical and research communities (English)

0 references

0 references

1 reference

based on heuristic

inferred from title

mitochondrial disease

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

Holger Prokisch

20

0 references

Maria Angela Diroma

object named as

Maria Angela Diroma

7

0 references

object named as

Jeremy Leipzig

4

0 references

Mannis van Oven

object named as

Mannis van Oven

19

0 references

William C Copeland

object named as

William C Copeland

18

0 references

object named as

Marni J Falk

1

0 references

Stephan Züchner

24

object named as

Stephan Zuchner

0 references

Sharon F. Terry

16

object named as

Sharon F Terry

0 references

author name string

Lishuang Shen

2

0 references

Michael Gonzalez

3

0 references

Marie T Lott

5

0 references

Alphons P M Stassen

6

0 references

Daniel Navarro-Gomez

8

0 references

Philip Yeske

9

0 references

Renkui Bai

10

0 references

Richard G Boles

11

0 references

Virginia Brilhante

12

0 references

David Ralph

13

0 references

Jeana T DaRe

14

0 references

Robert Shelton

15

0 references

Zhe Zhang

17

0 references

Douglas C Wallace

21

0 references

Marcella Attimonelli

22

0 references

Danuta Krotoski

23

0 references

Xiaowu Gai

25

0 references

language of work or name

0 references

publication date

March 2015

0 references

Molecular Genetics and Metabolism

1 reference

114

0 references

3

0 references

388-96

0 references

An integrated map of genetic variation from 1,092 human genomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512182

21 March 2017

Targeted capture and massively parallel sequencing of 12 human exomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512182

21 March 2017

The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512182

21 March 2017

Updated comprehensive phylogenetic tree of global human mitochondrial DNA variation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512182

21 March 2017

The RHNumtS compilation: features and bioinformatics approaches to locate and quantify Human NumtS

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512182

21 March 2017

mtDNA Variation and Analysis Using Mitomap and Mitomaster

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512182

28 September 2017

Extraction and annotation of human mitochondrial genomes from 1000 Genomes Whole Exome Sequencing data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512182

28 September 2017

Clinical phenotype-based gene prioritization: an initial study using semantic similarity and the human phenotype ontology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512182

28 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512182

28 September 2017

Integrated transcriptome analysis across mitochondrial disease etiologies and tissues improves understanding of common cellular adaptations to respiratory chain dysfunction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512182

28 September 2017

MitoBreak: the mitochondrial DNA breakpoints database

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512182

28 September 2017

Targeted exome sequencing of suspected mitochondrial disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512182

28 September 2017

Molecular genetic testing for mitochondrial disease: from one generation to the next

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512182

28 September 2017

Monogenic mitochondrial disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512182

28 September 2017

HmtDB, a genomic resource for mitochondrion-based human variability studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512182

28 September 2017

The reference human nuclear mitochondrial sequences compilation validated and implemented on the UCSC genome browser

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512182

28 September 2017

LOVD v.2.0: the next generation in gene variant databases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512182

28 September 2017

Consequences of mutations in human DNA polymerase gamma.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512182

28 September 2017

GEnomes Management Application (GEM.app): a new software tool for large-scale collaborative genome analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512182

31 May 2018

Use of whole-exome sequencing to determine the genetic basis of multiple mitochondrial respiratory chain complex deficiencies.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512182

28 November 2018

Electronic consent channels: preserving patient privacy without handcuffing researchers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512182

28 November 2018

mtDNA tree Build 17 (18 Feb 2016)

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2014.11.016

7 January 2021

Identifiers

10.1016/J.YMGME.2014.11.016

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

release_aacqgr55zzfstjooo336l6zlv4

0 references

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q27008228&oldid=2032614030"