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Targeted resequencing of candidate genes using Selector Probes

Johansson, Henrik (author)
Uppsala universitet,Institutionen för immunologi, genetik och patologi
Isaksson, Magnus (author)
Uppsala universitet,Institutionen för immunologi, genetik och patologi
Sörqvist, Elin Falk (author)
Uppsala universitet,Molekylära verktyg,Forskargrupp Mats Nilsson
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Roos, F. (author)
Uppsala universitet,Institutionen för immunologi, genetik och patologi
Stenberg, Johan (author)
Uppsala universitet,Institutionen för immunologi, genetik och patologi
Sjöblom, Tobias (author)
Uppsala universitet,Genomik,Forskargrupp Sjöblom
Botling, Johan (author)
Uppsala universitet,Molekylär och morfologisk patologi,Forskargrupp Botling
Micke, Patrick (author)
Uppsala universitet,Molekylär och morfologisk patologi,Forskargrupp Botling
Edlund, Karolina (author)
Uppsala universitet,Molekylär och morfologisk patologi,Forskargrupp Botling
Fredriksson, S. (author)
Göransson Kultima, Hanna (author)
Uppsala universitet,Institutionen för medicinska vetenskaper,Cancer Pharmacology and Computational medicine
Ericsson, Olle (author)
Uppsala universitet,Institutionen för immunologi, genetik och patologi
Nilsson, Mats (author)
Uppsala universitet,Molekylära verktyg,Forskargrupp Mats Nilsson
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 (creator_code:org_t)
2010-11-08
2011
English.
In: Nucleic Acids Research. - : Oxford University Press (OUP). - 0305-1048 .- 1362-4962. ; 39:2, s. e8-
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Targeted genome enrichment is a powerful tool for making use of the massive throughput of novel DNA-sequencing instruments. We herein present a simple and scalable protocol for multiplex amplification of target regions based on the Selector technique. The updated version exhibits improved coverage and compatibility with next-generation-sequencing (NGS) library-construction procedures for shotgun sequencing with NGS platforms. To demonstrate the performance of the technique, all 501 exons from 28 genes frequently involved in cancer were enriched for and sequenced in specimens derived from cell lines and tumor biopsies. DNA from both fresh frozen and formalin-fixed paraffin-embedded biopsies were analyzed and 94 specificity and 98 coverage of the targeted region was achieved. Reproducibility between replicates was high (R 2=0, 98) and readily enabled detection of copy-number variations. The procedure can be carried out in <24 h and does not require any dedicated instrumentation.

Keyword

Resequencing
Targeted
Next generation sequencing
Selectors
Cancer
Tumor
FFPE
MEDICINE
MEDICIN
Medical Genetics
Medicinsk genetik

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ref (subject category)
art (subject category)

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