Variant identification in multi-sample pools by illumina genome analyzer sequencing.

Margraf, Rebecca L; Durtschi, Jacob D; Dames, Shale; Pattison, David C; Stephens, Jack E; Voelkerding, Karl V

Margraf, Rebecca L; Durtschi, Jacob D; Dames, Shale; Pattison, David C; Stephens, Jack E; Voelkerding, Karl V.

Affiliation

Margraf RL; ARUP Institute for Clinical & Experimental Pathology®, Salt Lake City, Utah, USA. rebecca.margraf@aruplab.com

J Biomol Tech ; 22(2): 74-84, 2011 Jul.

Article in En | MEDLINE | ID: mdl-21738440

Subject(s)

Sequence Analysis, DNA/instrumentation; Data Interpretation, Statistical; Genetic Variation; Humans; Proto-Oncogene Mas; Proto-Oncogene Proteins c-ret/genetics; Reference Values; Reproducibility of Results; Sequence Analysis, DNA/methods

Key words

Illumina Genome Analyzer; RET; massively parallel sequencing; next generation sequencing; pooling

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sequence Analysis, DNA Type of study: Diagnostic_studies / Guideline / Prognostic_studies Limits: Humans Language: En Journal: J Biomol Tech Journal subject: BIOTECNOLOGIA Year: 2011 Document type: Article Affiliation country: United States

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