Accurate clinical detection of exon copy number variants in a targeted NGS panel using DECoN.
about
The ICR96 exon CNV validation series: a resource for orthogonal assessment of exon CNV calling in NGS dataAssessment of the incorporation of CNV surveillance into gene panel next-generation sequencing testing for inherited retinal diseases.CoverView: a sequence quality evaluation tool for next generation sequencing data.A Whole Germline BRCA2 Gene Deletion: How to Learn from CNV In Silico Analysis.The ICR639 CPG NGS validation series: A resource to assess analytical sensitivity of cancer predisposition gene testing
P2860
Accurate clinical detection of exon copy number variants in a targeted NGS panel using DECoN.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
Accurate clinical detection of ...... argeted NGS panel using DECoN.
@en
type
label
Accurate clinical detection of ...... argeted NGS panel using DECoN.
@en
prefLabel
Accurate clinical detection of ...... argeted NGS panel using DECoN.
@en
P2093
P2860
P50
P1476
Accurate clinical detection of ...... argeted NGS panel using DECoN.
@en
P2093
Anna Fowler
Elise Ruark
Gerton Lunter
Matthew Clarke
Sheila Seal
P2860
P356
10.12688/WELLCOMEOPENRES.10069.1
P577
2016-11-25T00:00:00Z