AbCD: arbitrary coverage design for sequencing-based genetic studies. - Wikidata - awgldk - TriplyDB

AbCD: arbitrary coverage design for sequencing-based genetic studies.

AbCD: arbitrary coverage design for sequencing-based genetic studies.

http://www.wikidata.org/entity/Q41143684

about

Imputation of coding variants in African Americans: better performance using data from the exome sequencing project Exploring the occurrence of classic selective sweeps in humans using whole-genome sequencing data sets.Likelihood-based complex trait association testing for arbitrary depth sequencing data.Association studies with imputed variants using expectation-maximization likelihood-ratio tests.Advances in biotechnology and informatics to link variation in the genome to phenotypes in plants and animals Systematic review of next-generation sequencing simulators: computational tools, features and perspectives.Low-, high-coverage, and two-stage DNA sequencing in the design of the genetic association study.Analysis of genetic and nongenetic factors influencing triglycerides-lowering drug effects based on paired observations

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P2860

AbCD: arbitrary coverage design for sequencing-based genetic studies.

http://www.wikidata.org/entity/Q41143684

description

2013 nî lūn-bûn

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2013年の論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年论文

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2013年论文

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2013年论文

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name

AbCD: arbitrary coverage design for sequencing-based genetic studies.

@en

AbCD: arbitrary coverage design for sequencing-based genetic studies.

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type

label

AbCD: arbitrary coverage design for sequencing-based genetic studies.

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AbCD: arbitrary coverage design for sequencing-based genetic studies.

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AbCD: arbitrary coverage design for sequencing-based genetic studies.

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AbCD: arbitrary coverage design for sequencing-based genetic studies.

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AbCD: arbitrary coverage design for sequencing-based genetic studies.

@en

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Kuan-Chieh Huang

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

Yun Li

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

Yunfei Wang

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

Zheng Xu

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

P2860

Exome sequencing identifies the cause of a mendelian disorder

MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes

Sequencing technologies - the next generation

Next-generation DNA sequencing methods

Exome sequencing as a tool for Mendelian disease gene discovery

Linkage disequilibrium in humans: models and data.

Accurate detection and genotyping of SNPs utilizing population sequencing data

Finding disease variants in Mendelian disorders by using sequence data: methods and applications.

Efficiency and power as a function of sequence coverage, SNP array density, and imputation.

Next-generation DNA sequencing techniques.

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799-801

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scholarly article

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10.1093/BIOINFORMATICS/BTT041

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6

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29

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Gonçalo Abecasis

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2013-01-28T00:00:00Z

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235379415

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