Accurate whole genome sequencing and haplotyping from10-20 human cells

Recent advances in whole genome sequencing have brought the vision of personal genomics and genomic medicine closer to reality. However, current methods lack clinical accuracy and the ability to describe the context (haplotypes) in which genome variants co-occur in a cost-effective manner. Here we d...

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Bibliografiske detaljer
Main Authors: Peters, Brock A., Kermani, Bahram G., Sparks, Andrew B., Alferov, Oleg, Hong, Peter, Alexeev, Andrei, Jiang, Yuan, Dahl, Fredrik, Tang, Y. Tom, Haas, Juergen, Robasky, Kimberly, Zaranek, Alexander Wait, Lee, Je-Hyuk, Ball, Madeleine Price, Peterson, Joseph E., Perazich, Helena, Yeung, George, Liu, Jia, Chen, Linsu, Kennemer, Michael I., Pothuraju, Kaliprasad, Konvicka, Karel, Tsoupko-Sitnikov, Mike, Pant, Krishna P., Ebert, Jessica C., Nilsen, Geoffrey B., Baccash, Jonathan, Halpern, Aaron L., Church, George M., Drmanac, Radoje
Format: Artigo
Sprog:Inglês
Udgivet: 2012
Fag:
Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3397394/
https://ncbi.nlm.nih.gov/pubmed/22785314
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nature11236
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