Molecular characterization of ring chromosome 18 by low-coverage next generation sequencing.

about

Clinical application of whole-genome low-coverage next-generation sequencing to detect and characterize balanced chromosomal translocations.

P2860

Q52674026-50038C5B-5177-451C-8DC0-966F67DF21EA

P2860

Molecular characterization of ring chromosome 18 by low-coverage next generation sequencing.

Item

http://www.wikidata.org/entity/Q35724944

description

2015 nî lūn-bûn

@nan

2015年の論文

@ja

2015年論文

@yue

2015年論文

@zh-hant

2015年論文

@zh-hk

2015年論文

@zh-mo

2015年論文

@zh-tw

2015年论文

@wuu

2015年论文

@zh

2015年论文

@zh-cn

name

Molecular characterization of ...... ge next generation sequencing.

@ast

Molecular characterization of ...... ge next generation sequencing.

@en

type

Item

label

Molecular characterization of ...... ge next generation sequencing.

@ast

Molecular characterization of ...... ge next generation sequencing.

@en

prefLabel

Molecular characterization of ...... ge next generation sequencing.

@ast

Molecular characterization of ...... ge next generation sequencing.

@en

P1476

Molecular characterization of ...... ge next generation sequencing.

@en

P2093

Cuiyun Liu

http://www.w3.org/2001/XMLSchema#string

Dingyuan Ma

http://www.w3.org/2001/XMLSchema#string

Dong Liang

http://www.w3.org/2001/XMLSchema#string

Ping Hu

http://www.w3.org/2001/XMLSchema#string

Ruihong Sun

http://www.w3.org/2001/XMLSchema#string

Xiuqing Ji

http://www.w3.org/2001/XMLSchema#string

Yan Wang

http://www.w3.org/2001/XMLSchema#string

Zhengfeng Xu

http://www.w3.org/2001/XMLSchema#string

P2860

Characterization of complex chromosomal rearrangements by targeted capture and next-generation sequencing

Fast and accurate short read alignment with Burrows-Wheeler transform

Characterization of human chromosomal material exchange with regard to the chromosome translocations using next-generation sequencing data

Bellerophon: a hybrid method for detecting interchromosomal rearrangements at base pair resolution using next-generation sequencing data

Next-generation sequencing strategies enable routine detection of balanced chromosome rearrangements for clinical diagnostics and genetic research.

Breakpoint analysis of balanced chromosome rearrangements by next-generation paired-end sequencing.

Observation and prediction of recurrent human translocations mediated by NAHR between nonhomologous chromosomes.

A robust approach for blind detection of balanced chromosomal rearrangements with whole-genome low-coverage sequencing.

Mechanisms for recurrent and complex human genomic rearrangements.

Clinical and molecular-cytogenetic studies in seven patients with ring chromosome 18.

P2888

s12881-015-0206-x

P304

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1186/S12881-015-0206-X

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P577

2015-07-30T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

280585616

http://www.w3.org/2001/XMLSchema#string

P6179

1033901731

http://www.w3.org/2001/XMLSchema#string

P698

26224010

http://www.w3.org/2001/XMLSchema#string

P932

4557216

http://www.w3.org/2001/XMLSchema#string

Molecular characterization of ring chromosome 18 by low-coverage next generation sequencing.

about

P2860

P2860

Molecular characterization of ring chromosome 18 by low-coverage next generation sequencing.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P478

P577

P5875

P6179

P698

P932

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P478

P577

P5875

P6179

P698

P932