about
Integrating next-generation sequencing into clinical oncology: strategies, promises and pitfallsBig Data Analytics for Genomic MedicineLeveraging splice-affecting variant predictors and a minigene validation system to identify Mendelian disease-causing variants among exon-captured variants of uncertain significance.Accurate clinical detection of exon copy number variants in a targeted NGS panel using DECoN.OpEx - a validated, automated pipeline optimised for clinical exome sequence analysis.MECP2 variation in Rett syndrome - an overview of current coverage of genetic and phenotype data within existing databasesWhole-Exome Sequencing Reveals Uncaptured Variation and Distinct Ancestry in the Southern African Population of Botswana.A machine learning model to determine the accuracy of variant calls in capture-based next generation sequencing.
P2860
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P2860
description
2016 nî lūn-bûn
@nan
2016 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2016 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2016年の論文
@ja
2016年学术文章
@wuu
2016年学术文章
@zh-cn
2016年学术文章
@zh-hans
2016年学术文章
@zh-my
2016年学术文章
@zh-sg
2016年學術文章
@yue
name
Novel bioinformatic developments for exome sequencing
@ast
Novel bioinformatic developments for exome sequencing
@en
Novel bioinformatic developments for exome sequencing
@nl
type
label
Novel bioinformatic developments for exome sequencing
@ast
Novel bioinformatic developments for exome sequencing
@en
Novel bioinformatic developments for exome sequencing
@nl
prefLabel
Novel bioinformatic developments for exome sequencing
@ast
Novel bioinformatic developments for exome sequencing
@en
Novel bioinformatic developments for exome sequencing
@nl
P2860
P3181
P1433
P1476
Novel bioinformatic developments for exome sequencing
@en
P2093
Stefan H Lelieveld
P2860
P2888
P304
P3181
P356
10.1007/S00439-016-1658-6
P407
P577
2016-06-01T00:00:00Z
P6179
1043091107