Multiplexed array-based and in-solution genomic enrichment for flexible and cost-effective targeted next-generation sequencing (Q34066566)

30 July 2017

Multiplexed array-based and in-solution genomic enrichment for flexible and cost-effective targeted next-generation sequencing (English)

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30 July 2017

Barbara Hrdlickova

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Michal Mokry

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Michal Mokry

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Isaac J Nijman

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Isaac J Nijman

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author name string

Magdalena Harakalova

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30 July 2017

Ivo Renkens

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30 July 2017

Karen Duran

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30 July 2017

Henk van Roekel

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30 July 2017

Nico Lansu

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30 July 2017

Mark van Roosmalen

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30 July 2017

Ewart de Bruijn

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30 July 2017

Wigard P Kloosterman

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30 July 2017

Edwin Cuppen

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30 July 2017

3 November 2011

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30 July 2017

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30 July 2017

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30 July 2017

1870-1886

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https://scigraph.springernature.com/pub.10.1038/nprot.2011.396

30 July 2017

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cites work

The diploid genome sequence of an Asian individual

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Resequencing of 200 human exomes identifies an excess of low-frequency non-synonymous coding variants

21 January 2018

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https://api.crossref.org/works/10.1038%2FNPROT.2011.396

Sequencing technologies - the next generation

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A de novo paradigm for mental retardation.

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A map of human genome variation from population-scale sequencing

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Target-enrichment strategies for next-generation sequencing

21 January 2018

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https://api.crossref.org/works/10.1038%2FNPROT.2011.396

Hybrid selection of discrete genomic intervals on custom-designed microarrays for massively parallel sequencing

21 January 2018

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https://api.crossref.org/works/10.1038%2FNPROT.2011.396

Mutation discovery by targeted genomic enrichment of multiplexed barcoded samples

21 January 2018

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https://api.crossref.org/works/10.1038%2FNPROT.2011.396

Frequent mutation of BAP1 in metastasizing uveal melanomas

21 January 2018

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https://api.crossref.org/works/10.1038%2FNPROT.2011.396

Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2011.396

Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2011.396

Exome sequencing identifies WDR35 variants involved in Sensenbrenner syndrome

21 January 2018

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https://api.crossref.org/works/10.1038%2FNPROT.2011.396

Exome sequencing, ANGPTL3 mutations, and familial combined hypolipidemia

21 January 2018

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Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations

21 January 2018

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Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome

21 January 2018

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https://api.crossref.org/works/10.1038%2FNPROT.2011.396

Combining target enrichment with barcode multiplexing for high throughput SNP discovery

21 January 2018

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https://api.crossref.org/works/10.1038%2FNPROT.2011.396

Systematic comparison of three genomic enrichment methods for massively parallel DNA sequencing

21 January 2018

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https://api.crossref.org/works/10.1038%2FNPROT.2011.396

Genomic DNA pooling strategy for next-generation sequencing-based rare variant discovery in abdominal aortic aneurysm regions of interest-challenges and limitations

21 January 2018

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https://api.crossref.org/works/10.1038%2FNPROT.2011.396

A scalable, fully automated process for construction of sequence-ready human exome targeted capture libraries

21 January 2018

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https://api.crossref.org/works/10.1038%2FNPROT.2011.396

Accurate SNP and mutation detection by targeted custom microarray-based genomic enrichment of short-fragment sequencing libraries

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2011.396

Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2011.396

Whole exome capture in solution with 3 Gbp of data

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2011.396

Microarray-based genomic selection for high-throughput resequencing.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2011.396

Targeted resequencing of candidate genes using selector probes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2011.396

Improving the efficiency of genomic loci capture using oligonucleotide arrays for high throughput resequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2011.396

Targeted enrichment of specific regions in the human genome by array hybridization

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2011.396

31 March 2020

Identifiers

DOI

10.1038/NPROT.2011.396

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Dimensions Publication ID

30 July 2017

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