Detection of genomic variations in BRCA1 and BRCA2 genes by long-range PCR and next-generation sequencing.

Detection of genomic variations in BRCA1 and BRCA2 genes by long-range PCR and next-generation sequencing.

Item
http://www.wikidata.org/entity/Q34198843
Cracking the Code of Human Diseases Using Next-Generation Sequencing: Applications, Challenges, and PerspectivesNext-generation sequencing of BRCA1/2 in breast cancer patients: potential effects on clinical decision-making using rapid, high-accuracy genetic results.Genetic testing in hereditary breast and ovarian cancer using massive parallel sequencingNext-generation sequencing meets genetic diagnostics: development of a comprehensive workflow for the analysis of BRCA1 and BRCA2 genes.Detection of novel mutations that cause autosomal dominant retinitis pigmentosa in candidate genes by long-range PCR amplification and next-generation sequencingThe highly prolific phenotype of Lacaune sheep is associated with an ectopic expression of the B4GALNT2 gene within the ovaryA reliable method for the detection of BRCA1 and BRCA2 mutations in fixed tumour tissue utilising multiplex PCR-based targeted next generation sequencingComparison of targeted next-generation sequencing and Sanger sequencing for the detection of PIK3CA mutations in breast cancergDNA enrichment by a transposase-based technology for NGS analysis of the whole sequence of BRCA1, BRCA2, and 9 genes involved in DNA damage repair.Application of next-generation sequencing in clinical oncology to advance personalized treatment of cancerOverview of molecular genetic diagnosis.A massive parallel sequencing workflow for diagnostic genetic testing of mismatch repair genes.Clinical impact on ovarian cancer patients of massive parallel sequencing for BRCA mutation detection: the experience at Gemelli hospital and a literature review.Clinical Applications of Next-Generation Sequencing in Cancer Diagnosis.Longrange PCR-based next-generation sequencing in pharmacokinetics and pharmacodynamics study of propofol among patients under general anaesthesia.Systematic detection of pathogenic alu element insertions in NGS-based diagnostic screens: the BRCA1/BRCA2 example.High-frequency, low-coverage "false positives" mutations may be true in GS Junior sequencing studies.
P2860

Detection of genomic variations in BRCA1 and BRCA2 genes by long-range PCR and next-generation sequencing.

Item
http://www.wikidata.org/entity/Q34198843
description
2012 nî lūn-bûn
@nan
2012 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի մարտին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
Detection of genomic variation ...... nd next-generation sequencing.
@ast
Detection of genomic variation ...... nd next-generation sequencing.
@en
Detection of genomic variation ...... nd next-generation sequencing.
@nl
type
label
Detection of genomic variation ...... nd next-generation sequencing.
@ast
Detection of genomic variation ...... nd next-generation sequencing.
@en
Detection of genomic variation ...... nd next-generation sequencing.
@nl
prefLabel
Detection of genomic variation ...... nd next-generation sequencing.
@ast
Detection of genomic variation ...... nd next-generation sequencing.
@en
Detection of genomic variation ...... nd next-generation sequencing.
@nl
P1433
P1476
P2093
P304
P31
P356
P433
P478
P577
P5875
P698
P356
P1433
P1476
Detection of genomic variation ...... nd next-generation sequencing.
@en
P2093
P304
P31
P356
10.1016/J.JMOLDX.2012.01.013
P433
P478
P577
P5875
P698