Literature DB >> 25762419

Whole-Exome Enrichment with the Roche NimbleGen SeqCap EZ Exome Library SR Platform.

Rui Chen1, Hogune Im1, Michael Snyder1.   

Abstract

Multiple platforms are available for whole-exome enrichment and sequencing (WES). This protocol is based on the Roche NimbleGen SeqCap EZ Exome Library SR platform, which enriches for ∼44 Mb of the human exonic regions. The SeqCap system uses 55- to 105-base DNA probes to capture known coding DNA sequences (CDS) from the NCBI Consensus CDS Database, RefSeq, and Sanger miRBase. The protocol can be performed at the benchside without the need for automation, and the resulting library can be used for targeted next-generation sequencing on an Illumina HiSeq 2000 sequencer.
© 2015 Cold Spring Harbor Laboratory Press.

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Year:  2015        PMID: 25762419      PMCID: PMC4490009          DOI: 10.1101/pdb.prot084855

Source DB:  PubMed          Journal:  Cold Spring Harb Protoc        ISSN: 1559-6095


  3 in total

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Authors:  Rui Chen; Hogune Im; Michael Snyder
Journal:  Cold Spring Harb Protoc       Date:  2015-03-11

2.  Whole-Exome Enrichment with the Agilent SureSelect Human All Exon Platform.

Authors:  Rui Chen; Hogune Im; Michael Snyder
Journal:  Cold Spring Harb Protoc       Date:  2015-03-11

3.  Performance comparison of exome DNA sequencing technologies.

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  3 in total
  7 in total

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Journal:  Cancer Res       Date:  2022-04-01       Impact factor: 13.312

3.  Whole-Exome Enrichment with the Illumina TruSeq Exome Enrichment Platform.

Authors:  Rui Chen; Hogune Im; Michael Snyder
Journal:  Cold Spring Harb Protoc       Date:  2015-03-11

4.  Whole-Exome Enrichment with the Agilent SureSelect Human All Exon Platform.

Authors:  Rui Chen; Hogune Im; Michael Snyder
Journal:  Cold Spring Harb Protoc       Date:  2015-03-11

5.  LIFE-Seq: a universal Large Integrated DNA Fragment Enrichment Sequencing strategy for deciphering the transgene integration of genetically modified organisms.

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Journal:  Mol Med Rep       Date:  2017-02-17       Impact factor: 2.952

7.  Novel variants in the KERA gene cause autosomal recessive cornea plana in a Chinese family: A case report.

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  7 in total

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