(Q44030648)

29 November 2017

title

Multiplexed resequencing analysis to identify rare variants in pooled DNA with barcode indexing using next-generation sequencer (English)

1 reference

29 November 2017

Jun Mitsui

1

1 reference

29 November 2017

Yoko Fukuda

2

1 reference

29 November 2017

Kyo Azuma

3

1 reference

29 November 2017

Hirokazu Tozaki

4

1 reference

29 November 2017

Hiroyuki Ishiura

5

1 reference

29 November 2017

Yuji Takahashi

6

1 reference

29 November 2017

Jun Goto

7

1 reference

29 November 2017

Shoji Tsuji

8

1 reference

29 November 2017

publication date

20 May 2010

1 reference

Journal of Human Genetics

29 November 2017

published in

1 reference

29 November 2017

volume

55

1 reference

29 November 2017

issue

7

1 reference

29 November 2017

page(s)

448-455

1 reference

https://scigraph.springernature.com/pub.10.1038/jhg.2010.46

29 November 2017

exact match

0 references

cites work

Genetic mapping in human disease

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.46

Human genetic variation and its contribution to complex traits

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.46

Mutations in the glucocerebrosidase gene and Parkinson's disease in Ashkenazi Jews

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.46

Glucocerebrosidase mutations in subjects with parkinsonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.46

Mutations for Gaucher disease confer high susceptibility to Parkinson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.46

Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.46

Next-generation DNA sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.46

Identification of genetic variants using bar-coded multiplexed sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.46

Analysis and classification of 304 mutant alleles in patients with type 1 and type 3 Gaucher disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.46

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.46

Quantification of rare allelic variants from pooled genomic DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.46

21 January 2018

Identifiers

DOI

10.1038/JHG.2010.46

1 reference

29 November 2017

1 reference