Joint genotype calling with array and sequence data. - Wikidata - awgldk - TriplyDB

Joint genotype calling with array and sequence data.

Joint genotype calling with array and sequence data.

http://www.wikidata.org/entity/Q34347497

about

Fast imputation using medium or low-coverage sequence data.A general approach for haplotype phasing across the full spectrum of relatedness Genotype calling and phasing using next-generation sequencing reads and a haplotype scaffold.

P2860

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P2860

Joint genotype calling with array and sequence data.

http://www.wikidata.org/entity/Q34347497

description

2012 nî lūn-bûn

@nan

2012 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2012 թվականի հուլիսին 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

Joint genotype calling with array and sequence data.

@ast

Joint genotype calling with array and sequence data.

@en

Joint genotype calling with array and sequence data.

@nl

type

label

Joint genotype calling with array and sequence data.

@ast

Joint genotype calling with array and sequence data.

@en

Joint genotype calling with array and sequence data.

@nl

prefLabel

Joint genotype calling with array and sequence data.

@ast

Joint genotype calling with array and sequence data.

@en

Joint genotype calling with array and sequence data.

@nl

P1433

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P1476

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P2093

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P2860

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P698

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P356

P1433

Genetic Epidemiology

P1476

Joint genotype calling with array and sequence data.

@en

P2093

Jared O'Connell

http://www.w3.org/2001/XMLSchema#string

P2860

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

Hundreds of variants clustered in genomic loci and biological pathways affect human height

Stampy: a statistical algorithm for sensitive and fast mapping of Illumina sequence reads

Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke.

Comparing genotyping algorithms for Illumina's Infinium whole-genome SNP BeadChips.

Improving SNP discovery by base alignment quality.

A genotype calling algorithm for the Illumina BeadArray platform

GenoSNP: a variational Bayes within-sample SNP genotyping algorithm that does not require a reference population.

P304

527-537

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1002/GEPI.21657

http://www.w3.org/2001/XMLSchema#string

P433

6

http://www.w3.org/2001/XMLSchema#string

P478

36

http://www.w3.org/2001/XMLSchema#string

P50

Jonathan Marchini

P577

2012-07-20T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

229437404

http://www.w3.org/2001/XMLSchema#string

P698

22821426

http://www.w3.org/2001/XMLSchema#string