Robust identification of deletions in exome and genome sequence data based on clustering of Mendelian errors.

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Robust identification of deletions in exome and genome sequence data based on clustering of Mendelian errors.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年學術文章

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2018年學術文章

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Robust identification of delet ...... lustering of Mendelian errors.

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Robust identification of delet ...... lustering of Mendelian errors.

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label

Robust identification of delet ...... lustering of Mendelian errors.

@en

Robust identification of delet ...... lustering of Mendelian errors.

@nl

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Robust identification of delet ...... lustering of Mendelian errors.

@en

Robust identification of delet ...... lustering of Mendelian errors.

@nl

P1476

Robust identification of delet ...... clustering of Mendelian errors

@en

P2093

Andrew J Sharp

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Angela C Tai

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Bruce D Gelb

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Christine E Seidman

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Deepak Srivastava

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Elizabeth Goldmuntz

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Jason Homsy

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Jonathan G Seidman

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Joshua Gorham

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Marko T Boskovski

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P2860

LUMPY: a probabilistic framework for structural variant discovery.

Extensive sequencing of seven human genomes to characterize benchmark reference materials.

The 15q11.2 BP1-BP2 microdeletion syndrome: a review

Detection of Genomic Structural Variants from Next-Generation Sequencing Data

The contribution of de novo coding mutations to autism spectrum disorder

CNVnator: an approach to discover, genotype, and characterize typical and atypical CNVs from family and population genome sequencing

Origins and functional impact of copy number variation in the human genome

De novo mutations revealed by whole-exome sequencing are strongly associated with autism

Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations

Genome-wide mapping and assembly of structural variant breakpoints in the mouse genome

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870-881

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P31

scholarly article

P356

10.1002/HUMU.23419

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P433

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P478

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

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Kathryn B Manheimer

Felix Richter

P577

2018-03-22T00:00:00Z

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P698

29527824

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P932

6022753

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