VEGAWES: variational segmentation on whole exome sequencing for copy number detection

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VEGAWES: variational segmentation on whole exome sequencing for copy number detection

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VEGAWES: variational segmentation on whole exome sequencing for copy number detection

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VEGAWES: variational segmentation on whole exome sequencing for copy number detection

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VEGAWES: variational segmentation on whole exome sequencing for copy number detection

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VEGAWES: variational segmentation on whole exome sequencing for copy number detection

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VEGAWES: variational segmentation on whole exome sequencing for copy number detection

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VEGAWES: variational segmentation on whole exome sequencing for copy number detection

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P1476

VEGAWES: variational segmentation on whole exome sequencing for copy number detection

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P2093

Samreen Anjum

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P2860

Computational tools for copy number variation (CNV) detection using next-generation sequencing data: features and perspectives

VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing

Strong association of de novo copy number mutations with autism

Fast and accurate short read alignment with Burrows-Wheeler transform

Fast gapped-read alignment with Bowtie 2

The somatic genomic landscape of glioblastoma

The landscape of somatic copy-number alteration across human cancers.

Integrated detection and population-genetic analysis of SNPs and copy number variation

Circular binary segmentation for the analysis of array-based DNA copy number data

Using XHMM Software to Detect Copy Number Variation in Whole-Exome Sequencing Data.

P2888

s12859-015-0748-0

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315

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P31

scholarly article

P356

10.1186/S12859-015-0748-0

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P478

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P50

P577

2015-09-29T00:00:00Z

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282334001

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1019560439

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26416038

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4587906

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