(Q31075107)

16 August 2017

Reference genotype and exome data from an Australian Aboriginal population for health-based research (English)

1 reference

16 August 2017

6

1 reference

PubMed publication ID

28 June 2017

Richard W Francis

3

0 references

Denise Anderson

object named as

Denise Anderson

2

0 references

Jenefer Blackwell

7

object named as

Jenefer M Blackwell

1 reference

16 August 2017

Dave Tang

1

1 reference

16 August 2017

Genevieve Syn

4

1 reference

16 August 2017

Sarra E Jamieson

5

1 reference

16 August 2017

12 April 2016

1 reference

16 August 2017

1 reference

16 August 2017

3

1 reference

16 August 2017

160023

1 reference

Creative Commons Attribution 4.0 International

16 August 2017

start time

12 April 2016

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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1 reference

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The UK10K project identifies rare variants in health and disease

21 June 2018

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First genome-wide association study in an Australian aboriginal population provides insights into genetic risk factors for body mass index and type 2 diabetes

21 June 2018

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21 June 2018

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21 June 2018

1 reference

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4828942

Bpipe: a tool for running and managing bioinformatics pipelines

21 June 2018

1 reference

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Using Drosophila melanogaster as a Model for Genotoxic Chemical Mutational Studies with a New Program, SnpSift

21 June 2018

1 reference

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Exome sequencing as a tool for Mendelian disease gene discovery

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4828942

A framework for variation discovery and genotyping using next-generation DNA sequencing data

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4828942

Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4828942

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4828942

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4828942

BEDTools: a flexible suite of utilities for comparing genomic features

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4828942

Exome sequencing identifies the cause of a mendelian disorder

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4828942

The UCSC Genome Browser Database: update 2006

21 June 2018

1 reference

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The International HapMap Project

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4828942

dbSNP: the NCBI database of genetic variation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4828942

bam.iobio: a web-based, real-time, sequence alignment file inspector

21 June 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FSDATA.2016.23

21 January 2018

Identifiers

DOI

10.1038/SDATA.2016.23

1 reference

Dimensions Publication ID

16 August 2017

0 references

1 reference

16 August 2017

PubMed publication ID

27070114

1 reference