cnvScan: a CNV screening and annotation tool to improve the clinical utility of computational CNV prediction from exome sequencing data
about
Detection of genomic rearrangements from targeted resequencing data in Parkinson's disease patientsIntegrating Epigenomic Elements and GWASs Identifies BDNF Gene Affecting Bone Mineral Density and Osteoporotic Fracture Risk.A potential founder variant in CARMIL2/RLTPR in three Norwegian families with warts, molluscum contagiosum, and T-cell dysfunction.iCopyDAV: Integrated platform for copy number variations-Detection, annotation and visualization.Ximmer: A system for improving accuracy and consistency of CNV calling from exome data
P2860
cnvScan: a CNV screening and annotation tool to improve the clinical utility of computational CNV prediction from exome sequencing data
description
2016 nî lūn-bûn
@nan
2016 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2016 թվականի հունվարին հրատարակված գիտական հոդված
@hy
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
name
cnvScan: a CNV screening and a ...... ion from exome sequencing data
@ast
cnvScan: a CNV screening and a ...... ion from exome sequencing data
@en
type
label
cnvScan: a CNV screening and a ...... ion from exome sequencing data
@ast
cnvScan: a CNV screening and a ...... ion from exome sequencing data
@en
prefLabel
cnvScan: a CNV screening and a ...... ion from exome sequencing data
@ast
cnvScan: a CNV screening and a ...... ion from exome sequencing data
@en
P2093
P2860
P1433
P1476
cnvScan: a CNV screening and a ...... ion from exome sequencing data
@en
P2093
Asbjørg Stray-Pedersen
Hanne Sørmo Sorte
Olaug Kristin Rødningen
Pubudu Saneth Samarakoon
Robert Lyle
P2860
P2888
P356
10.1186/S12864-016-2374-2
P407
P577
2016-01-14T00:00:00Z
P5875
P6179
1044184707