Rare variant discovery by deep whole-genome sequencing of 1,070 Japanese individuals (Q28607995)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26292667%20AND%20SRC:MED&resulttype=core&format=json

22 February 2020

title

Rare variant discovery by deep whole-genome sequencing of 1,070 Japanese individuals (English)

1 reference

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22 February 2020

main subject

whole genome sequencing

1 reference

2

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22 February 2020

Hideyasu Kiyomoto

22

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22 February 2020

23

Atsushi Hozawa

1 reference

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22 February 2020

28

Nobuo Yaegashi

1 reference

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22 February 2020

author name string

Masao Nagasaki

1

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22 February 2020

Fumiki Katsuoka

3

1 reference

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22 February 2020

Naoki Nariai

4

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22 February 2020

Kaname Kojima

5

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22 February 2020

Yosuke Kawai

6

1 reference

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22 February 2020

Yumi Yamaguchi-Kabata

7

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22 February 2020

Junji Yokozawa

8

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22 February 2020

Inaho Danjoh

9

1 reference

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22 February 2020

Sakae Saito

10

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22 February 2020

Yukuto Sato

11

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22 February 2020

Takahiro Mimori

12

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22 February 2020

Kaoru Tsuda

13

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22 February 2020

Rumiko Saito

14

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22 February 2020

Xiaoqing Pan

15

1 reference

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22 February 2020

Satoshi Nishikawa

16

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22 February 2020

Shin Ito

17

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22 February 2020

Yoko Kuroki

18

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22 February 2020

Osamu Tanabe

19

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22 February 2020

Nobuo Fuse

20

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22 February 2020

Shinichi Kuriyama

21

1 reference

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22 February 2020

Naoko Minegishi

24

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22 February 2020

James Douglas Engel

25

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22 February 2020

Kengo Kinoshita

26

1 reference

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22 February 2020

Shigeo Kure

27

1 reference

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22 February 2020

Masayuki Yamamoto

30

1 reference

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22 February 2020

ToMMo Japanese Reference Panel Project

29

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22 February 2020

language of work or name

English

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publication date

21 August 2015

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22 February 2020

published in

Nature Communications

1 reference

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22 February 2020

volume

6

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22 February 2020

page(s)

8018

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Creative Commons Attribution 4.0 International

22 February 2020

copyright license

start time

21 August 2015

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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29 September 2017

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29 September 2017

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29 September 2017

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29 September 2017

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29 September 2017

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29 September 2017

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29 September 2017

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29 September 2017

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Long insert whole genome sequencing for copy number variant and translocation detection

29 September 2017

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29 September 2017

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29 September 2017

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29 September 2017

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29 September 2017

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ChromHMM: automating chromatin-state discovery and characterization

29 September 2017

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Analyzing and minimizing PCR amplification bias in Illumina sequencing libraries

29 September 2017

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A genome-wide association study identifies RNF213 as the first Moyamoya disease gene.

29 September 2017

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29 September 2017

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Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's disease

29 September 2017

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The HLA genomic loci map: expression, interaction, diversity and disease

29 September 2017

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Challenges and standards in integrating surveys of structural variation

29 September 2017

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A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC.

29 September 2017

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29 September 2017

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Simultaneous inference of selection and population growth from patterns of variation in the human genome

29 September 2017

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Reconstituting the frequency spectrum of ascertained single-nucleotide polymorphism data

29 September 2017

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Estimation of linkage between the Lutheran and the Lewis blood groups

29 September 2017

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The human gene mutation database

29 September 2017

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Immunobiological determinants in organ transplantation

29 September 2017

1 reference

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A genome wide association study of genetic loci that influence tumour biomarkers cancer antigen 19-9, carcinoembryonic antigen and α fetoprotein and their associations with cancer risk

29 September 2017

1 reference

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Improved whole-chromosome phasing for disease and population genetic studies

27 November 2018

1 reference

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27 November 2018

The IMGT/HLA database

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Birth prevalence of disorders detectable through newborn screening by race/ethnicity.

27 November 2018

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An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people

27 November 2018

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Heritability and familiality of type 2 diabetes and related quantitative traits in the Botnia Study

27 November 2018

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Newborn screening in Japan: restructuring for the new era.

27 November 2018

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Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction

27 November 2018

1 reference

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Genome-wide association study identifies novel loci associated with serum level of vitamin B12 in Chinese men

27 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26292667

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NCOMMS9018

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26292667%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

22 February 2020

ADS bibcode

2015NatCo...6.8018.

0 references

1029523624

0 references

1 reference

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26292667%20AND%20SRC:MED&resulttype=core&format=json

22 February 2020

PubMed publication ID

26292667

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26292667%20AND%20SRC:MED&resulttype=core&format=json