|
1
|
The White House Office of the Press
Secretary. Remarks by the President in State of the Union.
(2015-01-20) [2015-03-20]. urihttps://www.whitehouse.gov/the-press-office/2015/01/20/remarks-president-state-union-address-january-20-2015simplehttps://www.whitehouse.gov/the-press-office/2015/01/20/remarks-president-state-union-address-january-20-2015.
|
|
2
|
The White House Office of the Press
Secretary. FACT SHEET: President Obama's Precision Medicine
Initiative. (2015-01-30) [2015-03-20]. urihttps://www.whitehouse.gov/the-press-office/2015/01/30/fact-sheet-president-obama's-precision-medicine-initiativesimplehttps://www.whitehouse.gov/the-press-office/2015/01/30/fact-sheet-president-obama's-precision-medicine-initiative.
|
|
3
|
Yang Y, Muzny DM, Reid JG, Bainbridge MN,
Willis A, Ward PA, Braxton A, Beuten J, Xia F, Niu Z, et al:
Clinical whole-exome sequencing for the diagnosis of mendelian
disorders. N Engl J Med. 369:1502–1511. 2013.PubMed/NCBI View Article : Google Scholar
|
|
4
|
Lee H, Deignan JL, Dorrani N, Strom SP,
Kantarci S, Quintero-Rivera F, Das K, Toy T, Harry B, Yourshaw M,
et al: Clinical exome sequencing for genetic identification of rare
Mendelian disorders. JAMA. 312:1880–1887. 2014.PubMed/NCBI View Article : Google Scholar
|
|
5
|
Dewey FE, Grove ME, Pan C, Goldstein BA,
Bernstein JA, Chaib H, Merker JD, Goldfeder RL, Enns GM, David SP,
et al: Clinical interpretation and implications of whole-genome
sequencing. JAMA. 311:1035–1045. 2014.PubMed/NCBI View Article : Google Scholar
|
|
6
|
Hayes DN and Kim WY: The next steps in
next-gen sequencing of cancer genomes. J Clin Invest. 125:462–468.
2015.PubMed/NCBI View
Article : Google Scholar
|
|
7
|
Garraway LA: Genomics-driven oncology:
Framework for an emerging paradigm. J Clin Oncol. 31:1806–1814.
2013.PubMed/NCBI View Article : Google Scholar
|
|
8
|
Good BM, Ainscough BJ, McMichael JF, Su AI
and Griffith OL: Organizing knowledge to enable personalization of
medicine in cancer. Genome Biol. 15(438)2014.PubMed/NCBI View Article : Google Scholar
|
|
9
|
Griffith M, Miller CA, Griffith OL,
Krysiak K, Skidmore ZL, Ramu A, Walker JR, Dang HX, Trani L, Larson
DE, et al: Optimizing cancer genome sequencing and analysis. Cell
Syst. 1:210–223. 2015.PubMed/NCBI View Article : Google Scholar
|
|
10
|
Hyman DM, Solit DB, Arcila ME, Cheng DT,
Sabbatini P, Baselga J, Berger MF and Ladanyi M: Precision medicine
at memorial sloan kettering cancer center: Clinical next generation
sequencing enabling next-generation targeted therapy trials. Drug
Discov Today. 20:1422–1428. 2015.PubMed/NCBI View Article : Google Scholar
|
|
11
|
Hu Z, Sun R and Curtis C: A population
genetics perspective on the determinants of intra-tumor
heterogeneity. Biochim Biophys Acta Rev Cancer. 1867:109–126.
2017.PubMed/NCBI View Article : Google Scholar
|
|
12
|
Jamal-Hanjani M, Hackshaw A, Ngai Y, Shaw
J, Dive C, Quezada S, Middleton G, de Bruin E, Le Quesne J, Shafi
S, et al: Tracking genomic cancer evolution for precision medicine:
The lung TRACERx Study. PLoS Biol. 12(e1001906)2014.PubMed/NCBI View Article : Google Scholar
|
|
13
|
Patel NM, Michelini VV, Snell JM, Balu S,
Hoyle AP, Parker JS, Hayward MC, Eberhard DA, Salazar AH, McNeillie
P, et al: Enhancing next-generation sequencing-guided cancer care
through cognitive computing. Oncologist. 23:179–185.
2018.PubMed/NCBI View Article : Google Scholar
|
|
14
|
Pabinger S, Dander A, Fischer M, Snajder
R, Sperk M, Efremova M, Krabichler B, Speicher MR, Zschocke J and
Trajanoski Z: A survey of tools for variant analysis of
next-generation genome sequencing data. Brief Bioinform.
15:256–278. 2014.PubMed/NCBI View Article : Google Scholar
|
|
15
|
Oncologists partner with Watson on
genomics. Cancer Discov. 5(788)2015.PubMed/NCBI View Article : Google Scholar
|
|
16
|
Wrzeszczynski KO, Frank MO, Koyama T,
Rhrissorrakrai K, Robine N, Utro F, Emde AK, Chen BJ, Arora K, Shah
M, et al: Comparing sequencing assays and human-machine analyses in
actionable genomics for glioblastoma. Neurol Genet.
3(e164)2017.PubMed/NCBI View Article : Google Scholar
|
|
17
|
Itahashi K, Kondo S, Kubo T, Fujiwara Y,
Kato M, Ichikawa H, Koyama T, Tokumasu R, Xu J, Huettner CS, et al:
Evaluating clinical genome sequence analysis by Watson for
genomics. Front Med (Lausanne). 5(305)2018.PubMed/NCBI View Article : Google Scholar
|
