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Genome-Wide Copy Number Variation Detection Using NGS: Data Analysis and Interpretation.
Shen, Wei; Szankasi, Philippe; Durtschi, Jacob; Kelley, Todd W; Xu, Xinjie.
Affiliation
  • Shen W; Department of Pathology, University of Utah School of Medicine, Salt Lake City, UT, USA.
  • Szankasi P; ARUP Laboratories, Salt Lake City, UT, USA.
  • Durtschi J; ARUP Laboratories, Salt Lake City, UT, USA.
  • Kelley TW; Department of Pathology, University of Utah School of Medicine, Salt Lake City, UT, USA.
  • Xu X; Department of Pathology, University of Utah School of Medicine, Salt Lake City, UT, USA. xinjie.xu@aruplab.com.
Methods Mol Biol ; 1908: 113-124, 2019.
Article in En | MEDLINE | ID: mdl-30649724
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Software / Sequence Analysis, DNA / Loss of Heterozygosity / DNA Copy Number Variations / High-Throughput Nucleotide Sequencing / Neoplasms Type of study: Diagnostic_studies / Guideline Limits: Humans Language: En Journal: Methods Mol Biol Journal subject: BIOLOGIA MOLECULAR Year: 2019 Document type: Article Affiliation country: United States Country of publication: United States
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Software / Sequence Analysis, DNA / Loss of Heterozygosity / DNA Copy Number Variations / High-Throughput Nucleotide Sequencing / Neoplasms Type of study: Diagnostic_studies / Guideline Limits: Humans Language: En Journal: Methods Mol Biol Journal subject: BIOLOGIA MOLECULAR Year: 2019 Document type: Article Affiliation country: United States Country of publication: United States