Shendure J - Search Results

1

Needles in stacks of needles: finding disease-causal variants in a wealth of genomic data.

Cooper GM, Shendure J. Cooper GM, et al. Among authors: shendure j. Nat Rev Genet. 2011 Aug 18;12(9):628-40. doi: 10.1038/nrg3046. Nat Rev Genet. 2011. PMID: 21850043 Review.

2

Identification of foreign gene sequences by transcript filtering against the human genome.

Weber G, Shendure J, Tanenbaum DM, Church GM, Meyerson M. Weber G, et al. Among authors: shendure j. Nat Genet. 2002 Feb;30(2):141-2. doi: 10.1038/ng818. Epub 2002 Jan 14. Nat Genet. 2002. PMID: 11788827

3

Advanced sequencing technologies: methods and goals.

Shendure J, Mitra RD, Varma C, Church GM. Shendure J, et al. Nat Rev Genet. 2004 May;5(5):335-44. doi: 10.1038/nrg1325. Nat Rev Genet. 2004. PMID: 15143316 Review. No abstract available.

4

Multiplex amplification of large sets of human exons.

Porreca GJ, Zhang K, Li JB, Xie B, Austin D, Vassallo SL, LeProust EM, Peck BJ, Emig CJ, Dahl F, Gao Y, Church GM, Shendure J. Porreca GJ, et al. Among authors: shendure j. Nat Methods. 2007 Nov;4(11):931-6. doi: 10.1038/nmeth1110. Epub 2007 Oct 14. Nat Methods. 2007. PMID: 17934468

5

Massively parallel exon capture and library-free resequencing across 16 genomes.

Turner EH, Lee C, Ng SB, Nickerson DA, Shendure J. Turner EH, et al. Among authors: shendure j. Nat Methods. 2009 May;6(5):315-6. doi: 10.1038/nmeth.f.248. Epub 2009 Apr 6. Nat Methods. 2009. PMID: 19349981 Free PMC article. No abstract available.

6

Methods for genomic partitioning.

Turner EH, Ng SB, Nickerson DA, Shendure J. Turner EH, et al. Among authors: shendure j. Annu Rev Genomics Hum Genet. 2009;10:263-84. doi: 10.1146/annurev-genom-082908-150112. Annu Rev Genomics Hum Genet. 2009. PMID: 19630561 Review.

7

Targeted capture and massively parallel sequencing of 12 human exomes.

Ng SB, Turner EH, Robertson PD, Flygare SD, Bigham AW, Lee C, Shaffer T, Wong M, Bhattacharjee A, Eichler EE, Bamshad M, Nickerson DA, Shendure J. Ng SB, et al. Among authors: shendure j. Nature. 2009 Sep 10;461(7261):272-6. doi: 10.1038/nature08250. Epub 2009 Aug 16. Nature. 2009. PMID: 19684571 Free PMC article.

8

Exome sequencing identifies the cause of a mendelian disorder.

Ng SB, Buckingham KJ, Lee C, Bigham AW, Tabor HK, Dent KM, Huff CD, Shannon PT, Jabs EW, Nickerson DA, Shendure J, Bamshad MJ. Ng SB, et al. Among authors: shendure j. Nat Genet. 2010 Jan;42(1):30-5. doi: 10.1038/ng.499. Epub 2009 Nov 13. Nat Genet. 2010. PMID: 19915526 Free PMC article.

9

Journal club. A geneticist discusses a way to assess the effects of disease-causing gene mutations.

Shendure J. Shendure J. Nature. 2010 Jan 28;463(7280):405. doi: 10.1038/463405e. Nature. 2010. PMID: 20110948 No abstract available.

10

Single-nucleotide evolutionary constraint scores highlight disease-causing mutations.

Cooper GM, Goode DL, Ng SB, Sidow A, Bamshad MJ, Shendure J, Nickerson DA. Cooper GM, et al. Among authors: shendure j. Nat Methods. 2010 Apr;7(4):250-1. doi: 10.1038/nmeth0410-250. Nat Methods. 2010. PMID: 20354513 Free PMC article. No abstract available.

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