Houston Methodist variant viewer: An application to support clinical laboratory interpretation of next-generation sequencing data for cancer

Introduction: Next-generation-sequencing (NGS) is increasingly used in clinical and research protocols for patients with cancer. NGS assays are routinely used in clinical laboratories to detect mutations bearing on cancer diagnosis, prognosis and personalized therapy. A typical assay may interrogate...

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Main Authors: Paul A Christensen (Author), Yunyun Ni (Author), Feifei Bao (Author), Heather L Hendrickson (Author), Michael Greenwood (Author), Jessica S Thomas (Author), S Wesley Long (Author), Randall J Olsen (Author)
Formato: Libro
Publicado: Elsevier, 2017-01-01T00:00:00Z.
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Número de Clasificación: A1234.567
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