Literature DB >> 20953175

Mutation discovery by targeted genomic enrichment of multiplexed barcoded samples.

Isaäc J Nijman1, Michal Mokry, Ruben van Boxtel, Pim Toonen, Ewart de Bruijn, Edwin Cuppen.   

Abstract

Targeted genomic enrichment followed by next-generation DNA sequencing has dramatically increased efficiency of mutation-discovery efforts. We describe a protocol for genomic enrichment of pooled barcoded samples in a single assay that increases experimental flexibility and efficiency. We screened 770 genes (1.4 megabases) in thirty N-ethyl-N-nitrosourea (ENU)-mutagenized rats and identified known variants at >96% sensitivity as well as new mutations at a false positive rate < 1 in 8 megabases.

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Year:  2010        PMID: 20953175     DOI: 10.1038/nmeth.1516

Source DB:  PubMed          Journal:  Nat Methods        ISSN: 1548-7091            Impact factor:   28.547


  14 in total

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2.  Mismatch cleavage by single-strand specific nucleases.

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Review 3.  Target-enrichment strategies for next-generation sequencing.

Authors:  Lira Mamanova; Alison J Coffey; Carol E Scott; Iwanka Kozarewa; Emily H Turner; Akash Kumar; Eleanor Howard; Jay Shendure; Daniel J Turner
Journal:  Nat Methods       Date:  2010-02       Impact factor: 28.547

4.  Mapping short DNA sequencing reads and calling variants using mapping quality scores.

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Journal:  Genome Res       Date:  2008-08-19       Impact factor: 9.043

5.  Massively parallel sequencing of ataxia genes after array-based enrichment.

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Journal:  Hum Mutat       Date:  2010-04       Impact factor: 4.878

6.  Combining microarray-based genomic selection (MGS) with the Illumina Genome Analyzer platform to sequence diploid target regions.

Authors:  David T Okou; Adam E Locke; Karyn M Steinberg; Katie Hagen; Prashanth Athri; Amol C Shetty; Viren Patel; Michael E Zwick
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7.  Hybrid selection of discrete genomic intervals on custom-designed microarrays for massively parallel sequencing.

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8.  Efficient target-selected mutagenesis in Caenorhabditis elegans: toward a knockout for every gene.

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10.  Improved generation of rat gene knockouts by target-selected mutagenesis in mismatch repair-deficient animals.

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Journal:  BMC Genomics       Date:  2008-10-07       Impact factor: 3.969

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  35 in total

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Journal:  Nat Protoc       Date:  2011-11-03       Impact factor: 13.491

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Journal:  Nat Genet       Date:  2012-05-18       Impact factor: 38.330

3.  Next-generation sequencing strategies enable routine detection of balanced chromosome rearrangements for clinical diagnostics and genetic research.

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Journal:  Am J Hum Genet       Date:  2011-04-08       Impact factor: 11.025

4.  Rare variant discovery and calling by sequencing pooled samples with overlaps.

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5.  Identification of gene mutations in autosomal dominant polycystic kidney disease through targeted resequencing.

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6.  Inferring the evolution of the major histocompatibility complex of wild pigs and peccaries using hybridisation DNA capture-based sequencing.

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7.  Characterization of a de novo SCN8A mutation in a patient with epileptic encephalopathy.

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Review 8.  Novel sequencing-based strategies for high-throughput discovery of genetic mutations underlying inherited antibody deficiency disorders.

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9.  Efficient Genome-Wide Detection and Cataloging of EMS-Induced Mutations Using Exome Capture and Next-Generation Sequencing.

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Review 10.  Next-generation sequencing for research and diagnostics in kidney disease.

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Journal:  Nat Rev Nephrol       Date:  2014-06-10       Impact factor: 28.314

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