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Deep Sequencing of Patient Genomes for Disease Diagnosis: When Will It Become Routine? by Stephen F. Kingsmore, and Carol J. Saunders Sci Transl Med Volume.

Published byJosephine Fleming Modified over 8 years ago

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Presentation on theme: "Deep Sequencing of Patient Genomes for Disease Diagnosis: When Will It Become Routine? by Stephen F. Kingsmore, and Carol J. Saunders Sci Transl Med Volume."— Presentation transcript:

1 Deep Sequencing of Patient Genomes for Disease Diagnosis: When Will It Become Routine? by Stephen F. Kingsmore, and Carol J. Saunders Sci Transl Med Volume 3(87):87ps23-87ps23 June 15, 2011 Published by AAAS

2 Fig. 1. Contrasting technologies. Stephen F. Kingsmore and Carol J. Saunders Sci Transl Med 2011;3:87ps23 Published by AAAS

3 Fig. 2. Fast forward? Shown are the major similarities and differences in refinements needed for diagnostic use (DX) of WGS, exome-seq, and targeted NGS. The average depth of coverage differs in each approach. Stephen F. Kingsmore and Carol J. Saunders Sci Transl Med 2011;3:87ps23 Published by AAAS

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