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NGS method for parallel processing of high quality, damaged or fragmented input material using target enrichment

Lyander, Anna (author)
KTH,Genteknologi,Science for Life Laboratory, SciLifeLab,Science for Life Laboratory, KTH Royal Institute of Technology, Clinical Genomics Stockholm, School of Engineering Sciences in Chemistry, Biotechnology and Health, Stockholm, Sweden; Department of Microbiology, Science for Life Laboratory, Karolinska Institutet, Clinical Genomics Stockholm Tumor and Cell Biology, Stockholm, Sweden
Gellerbring, Anna (author)
Department of Microbiology, Science for Life Laboratory, Karolinska Institutet, Clinical Genomics Stockholm Tumor and Cell Biology, Stockholm, Sweden
Hägglund, Moa (author)
Department of Microbiology, Science for Life Laboratory, Karolinska Institutet, Clinical Genomics Stockholm Tumor and Cell Biology, Stockholm, Sweden
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Elhami, Keyvan (author)
Department of Microbiology, Science for Life Laboratory, Karolinska Institutet, Clinical Genomics Stockholm Tumor and Cell Biology, Stockholm, Sweden
Wirta, Valtteri (author)
KTH,Genteknologi,Science for Life Laboratory, SciLifeLab,Science for Life Laboratory, KTH Royal Institute of Technology, Clinical Genomics Stockholm, School of Engineering Sciences in Chemistry, Biotechnology and Health, Stockholm, Sweden; Department of Microbiology, Science for Life Laboratory, Karolinska Institutet, Clinical Genomics Stockholm Tumor and Cell Biology, Stockholm, Sweden
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 (creator_code:org_t)
Public Library of Science, 2024
2024
English.
In: PLOS ONE. - : Public Library of Science. - 1932-6203. ; 19:5 May
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Next-generation sequencing (NGS) has been increasingly popular in genomics studies over the last decade and is now commonly used in clinical applications for precision diagnostics. Many disease areas typically involve different kinds of sample specimens, sample qualities and quantities. The quality of the DNA can range from intact, high molecular weight molecules to degraded, damaged and very short molecules. The differences in quality and quantity pose challenges for downstream molecular analyses. To overcome the challenge with the need of different molecular methods for different types of samples, we have developed a joint procedure for preparing enriched DNA libraries from high molecular weight DNA and DNA from formalin-fixed, paraffin-embedded tissue, fresh frozen tissue material, as well as cell-free DNA.

Subject headings

NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)

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