(Q35548929)

8 August 2017

title

Sequence variants from whole genome sequencing a large group of Icelanders (English)

1 reference

8 August 2017

main subject

whole genome sequencing

1 reference

based on heuristic

inferred from title

author

Unnur Þorsteinsdóttir

16

Unnur Thorsteinsdottir

0 references

Augustine Kong

Augustine Kong

12

0 references

Patrick Sulem

Patrick Sulem

2

1 reference

8 August 2017

Daníel F. Guðbjartsson

1

Daniel F Gudbjartsson

1 reference

8 August 2017

17

Kari Stefansson

1 reference

8 August 2017

Hannes Helgason

3

1 reference

8 August 2017

Arnaldur Gylfason

4

1 reference

8 August 2017

Sigurjon A Gudjonsson

5

1 reference

8 August 2017

Florian Zink

6

1 reference

8 August 2017

Asmundur Oddson

7

1 reference

8 August 2017

Gisli Magnusson

8

1 reference

8 August 2017

Bjarni V Halldorsson

9

1 reference

8 August 2017

Eirikur Hjartarson

10

1 reference

8 August 2017

Gunnar Th Sigurdsson

11

1 reference

8 August 2017

Agnar Helgason

13

1 reference

8 August 2017

Gisli Masson

14

1 reference

8 August 2017

Olafur Th Magnusson

15

1 reference

8 August 2017

language of work or name

1 reference

25 March 2015

1 reference

8 August 2017

1 reference

8 August 2017

volume

2

1 reference

8 August 2017

page(s)

150011

1 reference

Creative Commons Attribution 4.0 International

8 August 2017

copyright license

start time

25 March 2015

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

exact match

https://scigraph.springernature.com/pub.10.1038/sdata.2015.11

0 references

cites work

Large-scale whole-genome sequencing of the Icelandic population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4413226

Whole-genome sequence variation, population structure and demographic history of the Dutch population

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4413226

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4413226

Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4413226

Huvariome: a web server resource of whole genome next-generation sequencing allelic frequencies to aid in pathological candidate gene selection

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4413226

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4413226

Evolution and functional impact of rare coding variation from deep sequencing of human exomes

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4413226

NCBI Reference Sequences (RefSeq): current status, new features and genome annotation policy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4413226

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4413226

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4413226

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4413226

Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4413226

Parental origin of sequence variants associated with complex diseases

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4413226

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4413226

Fast and accurate short read alignment with Burrows-Wheeler transform

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4413226

Detection of sharing by descent, long-range phasing and haplotype imputation

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4413226

Genome-wide nucleotide-level mammalian ancestor reconstruction

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4413226

Enredo and Pecan: genome-wide mammalian consistency-based multiple alignment with paralogs

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4413226

A second generation human haplotype map of over 3.1 million SNPs

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4413226

A new multipoint method for genome-wide association studies by imputation of genotypes

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4413226

The Sequence Ontology: a tool for the unification of genome annotations

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4413226

The human genome browser at UCSC

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4413226

dbSNP: the NCBI database of genetic variation

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4413226

Tandem repeats finder: a program to analyze DNA sequences

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4413226

Fine-scale recombination rate differences between sexes, populations and individuals

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4413226

Gene expression divergence in yeast is coupled to evolution of DNA-encoded nucleosome organization

26 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FSDATA.2015.11

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/SDATA.2015.11

1 reference

Dimensions Publication ID

8 August 2017

1026621968

0 references

Fatcat ID

release_6i6y6sn4ofgzblmqhdfito7b5a

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/6i6y6sn4ofgzblmqhdfito7b5a

mapped directly with Wikidata item

24 November 2022

based on heuristic

PMC publication ID

4413226

1 reference

8 August 2017

1 reference