SMASH, a fragmentation and sequencing method for genomic copy number analysis.

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Utility of single cell genomics in diagnostic evaluation of prostate cancer.iCopyDAV: Integrated platform for copy number variations-Detection, annotation and visualization.

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SMASH, a fragmentation and sequencing method for genomic copy number analysis.

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http://www.wikidata.org/entity/Q36022873

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2016 nî lūn-bûn

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2016年の論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年论文

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2016年论文

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2016年论文

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name

SMASH, a fragmentation and sequencing method for genomic copy number analysis.

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SMASH, a fragmentation and sequencing method for genomic copy number analysis.

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SMASH, a fragmentation and sequencing method for genomic copy number analysis.

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SMASH, a fragmentation and sequencing method for genomic copy number analysis.

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SMASH, a fragmentation and sequencing method for genomic copy number analysis.

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SMASH, a fragmentation and sequencing method for genomic copy number analysis.

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P1476

SMASH, a fragmentation and sequencing method for genomic copy number analysis.

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P2093

Beicong Ma

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

Dan Levy

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

Inessa Hakker

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

Jude Kendall

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

Linda Rodgers

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

Michael Ronemus

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

Peter Andrews

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

Zihua Wang

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

P2860

Ultrafast and memory-efficient alignment of short DNA sequences to the human genome

Strong association of de novo copy number mutations with autism

Structural variation of chromosomes in autism spectrum disorder

CNVs: harbingers of a rare variant revolution in psychiatric genetics

Serial analysis of gene expression

The Sequence Alignment/Map format and SAMtools

Detection of large-scale variation in the human genome

Large-scale copy number polymorphism in the human genome

Strong association of de novo copy number mutations with sporadic schizophrenia

Tumour evolution inferred by single-cell sequencing

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844-851

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scholarly article

P356

10.1101/GR.201491.115

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P478

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Michael Wigler

P577

2016-04-14T00:00:00Z

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27197213

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P932

4889966

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SMASH, a fragmentation and sequencing method for genomic copy number analysis.

about

P2860

P2860

SMASH, a fragmentation and sequencing method for genomic copy number analysis.

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P1476

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P2860

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P1476

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P932