Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1975 1
2005 1
2006 1
2007 1
2009 2
2010 1
2011 2
2012 3
2013 2
2014 2
2015 2
2016 2
2018 2
2021 2
Text availability
Article attribute
Article type
Publication date

Search Results

22 results
Results by year
Filters applied: . Clear all
Page 1
Detecting ultralow-frequency mutations by Duplex Sequencing.
Kennedy SR, Schmitt MW, Fox EJ, Kohrn BF, Salk JJ, Ahn EH, Prindle MJ, Kuong KJ, Shen JC, Risques RA, Loeb LA. Kennedy SR, et al. Among authors: schmitt mw. Nat Protoc. 2014 Nov;9(11):2586-606. doi: 10.1038/nprot.2014.170. Epub 2014 Oct 9. Nat Protoc. 2014. PMID: 25299156 Free PMC article.
Detection of ultra-rare mutations by next-generation sequencing.
Schmitt MW, Kennedy SR, Salk JJ, Fox EJ, Hiatt JB, Loeb LA. Schmitt MW, et al. Proc Natl Acad Sci U S A. 2012 Sep 4;109(36):14508-13. doi: 10.1073/pnas.1208715109. Epub 2012 Aug 1. Proc Natl Acad Sci U S A. 2012. PMID: 22853953 Free PMC article.
Risks of double-counting in deep sequencing.
Schmitt MW, Fox EJ, Salk JJ. Schmitt MW, et al. Proc Natl Acad Sci U S A. 2014 Apr 22;111(16):E1560. doi: 10.1073/pnas.1400941111. Epub 2014 Mar 20. Proc Natl Acad Sci U S A. 2014. PMID: 24706907 Free PMC article. No abstract available.
Implications of genetic heterogeneity in cancer.
Schmitt MW, Prindle MJ, Loeb LA. Schmitt MW, et al. Ann N Y Acad Sci. 2012 Sep;1267:110-6. doi: 10.1111/j.1749-6632.2012.06590.x. Ann N Y Acad Sci. 2012. PMID: 22954224 Free PMC article.
22 results
You have reached the last page of results. A maximum of 10,000 results are available.
Jump to page