Enriching targeted sequencing experiments for rare disease alleles.
about
Single Nucleotide Polymorphism (SNP) Detection and Genotype Calling from Massively Parallel Sequencing (MPS) DataGWAS to Sequencing: Divergence in Study Design and AnalysisSEQCHIP: a powerful method to integrate sequence and genotype data for the detection of rare variant associations.SeqSIMLA: a sequence and phenotype simulation tool for complex disease studiesThe impact of genomics on pediatric research and medicine.Optimized selection of unrelated subjects for whole-genome sequencing studies of rare high-penetrance alleles.
P2860
Enriching targeted sequencing experiments for rare disease alleles.
description
2011 nî lūn-bûn
@nan
2011 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Enriching targeted sequencing experiments for rare disease alleles.
@ast
Enriching targeted sequencing experiments for rare disease alleles.
@en
type
label
Enriching targeted sequencing experiments for rare disease alleles.
@ast
Enriching targeted sequencing experiments for rare disease alleles.
@en
prefLabel
Enriching targeted sequencing experiments for rare disease alleles.
@ast
Enriching targeted sequencing experiments for rare disease alleles.
@en
P2860
P356
P1433
P1476
Enriching targeted sequencing experiments for rare disease alleles
@en
P2093
Todd L Edwards
P2860
P304
P356
10.1093/BIOINFORMATICS/BTR324
P407
P50
P577
2011-06-23T00:00:00Z