Effect of Next-Generation Exome Sequencing Depth for Discovery of Diagnostic Variants.

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Amplicon-based semiconductor sequencing of human exomes: performance evaluation and optimization strategies Novel applications of next-generation sequencing in breast cancer research

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Effect of Next-Generation Exome Sequencing Depth for Discovery of Diagnostic Variants.

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2015 nî lūn-bûn

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Effect of Next-Generation Exome Sequencing Depth for Discovery of Diagnostic Variants.

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Effect of Next-Generation Exome Sequencing Depth for Discovery of Diagnostic Variants.

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Effect of Next-Generation Exome Sequencing Depth for Discovery of Diagnostic Variants.

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Effect of Next-Generation Exome Sequencing Depth for Discovery of Diagnostic Variants.

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Effect of Next-Generation Exome Sequencing Depth for Discovery of Diagnostic Variants.

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Effect of Next-Generation Exome Sequencing Depth for Discovery of Diagnostic Variants.

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P1476

Effect of Next-Generation Exome Sequencing Depth for Discovery of Diagnostic Variants.

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Jihyun Kim

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KiYoung Lee

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Kyung Kim

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Moon-Woo Seong

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Rae Woong Park

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Sangseob Leem

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Sung Sup Park

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Won Park

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Won-Hyong Chung

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Genetic diagnosis by whole exome capture and massively parallel DNA sequencing

Accurate and comprehensive sequencing of personal genomes

Targeted capture and massively parallel sequencing of 12 human exomes

Aspects of coverage in medical DNA sequencing

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

The Sequence Alignment/Map format and SAMtools

A donor splice site mutation in the parathyroid hormone gene is associated with autosomal recessive hypoparathyroidism

A splice-site mutation in GABRG2 associated with childhood absence epilepsy and febrile convulsions

Exome sequencing identifies frequent mutation of ARID1A in molecular subtypes of gastric cancer

Fast and accurate long-read alignment with Burrows-Wheeler transform

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31-39

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scholarly article

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10.5808/GI.2015.13.2.31

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Namshin Kim

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2015-06-30T00:00:00Z

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26175660

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Effect of Next-Generation Exome Sequencing Depth for Discovery of Diagnostic Variants.

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P2860

Effect of Next-Generation Exome Sequencing Depth for Discovery of Diagnostic Variants.

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P1476

P2093

P2860

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P577

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