Zwick ME - Search Results

1

PEMapper and PECaller provide a simplified approach to whole-genome sequencing.

Johnston HR, Chopra P, Wingo TS, Patel V; International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome; Epstein MP, Mulle JG, Warren ST, Zwick ME, Cutler DJ. Johnston HR, et al. Among authors: zwick me. Proc Natl Acad Sci U S A. 2017 Mar 7;114(10):E1923-E1932. doi: 10.1073/pnas.1618065114. Epub 2017 Feb 21. Proc Natl Acad Sci U S A. 2017. PMID: 28223510 Free PMC article.

2

Haplotype inference in random population samples.

Lin S, Cutler DJ, Zwick ME, Chakravarti A. Lin S, et al. Among authors: zwick me. Am J Hum Genet. 2002 Nov;71(5):1129-37. doi: 10.1086/344347. Epub 2002 Oct 17. Am J Hum Genet. 2002. PMID: 12386835 Free PMC article.

3

Discrepancies in dbSNP confirmation rates and allele frequency distributions from varying genotyping error rates and patterns.

Mitchell AA, Zwick ME, Chakravarti A, Cutler DJ. Mitchell AA, et al. Among authors: zwick me. Bioinformatics. 2004 May 1;20(7):1022-32. doi: 10.1093/bioinformatics/bth034. Epub 2004 Feb 5. Bioinformatics. 2004. PMID: 14764571

4

Microarray-based resequencing of multiple Bacillus anthracis isolates.

Zwick ME, Mcafee F, Cutler DJ, Read TD, Ravel J, Bowman GR, Galloway DR, Mateczun A. Zwick ME, et al. Genome Biol. 2005;6(1):R10. doi: 10.1186/gb-2004-6-1-r10. Epub 2004 Dec 17. Genome Biol. 2005. PMID: 15642093 Free PMC article.

5

Microarray-based genomic selection for high-throughput resequencing.

Okou DT, Steinberg KM, Middle C, Cutler DJ, Albert TJ, Zwick ME. Okou DT, et al. Among authors: zwick me. Nat Methods. 2007 Nov;4(11):907-9. doi: 10.1038/nmeth1109. Epub 2007 Oct 14. Nat Methods. 2007. PMID: 17934469

6

Microarray-based mutation detection in the dystrophin gene.

Hegde MR, Chin EL, Mulle JG, Okou DT, Warren ST, Zwick ME. Hegde MR, et al. Among authors: zwick me. Hum Mutat. 2008 Sep;29(9):1091-9. doi: 10.1002/humu.20831. Hum Mutat. 2008. PMID: 18663755 Free PMC article.

7

Combining microarray-based genomic selection (MGS) with the Illumina Genome Analyzer platform to sequence diploid target regions.

Okou DT, Locke AE, Steinberg KM, Hagen K, Athri P, Shetty AC, Patel V, Zwick ME. Okou DT, et al. Among authors: zwick me. Ann Hum Genet. 2009 Sep;73(Pt 5):502-13. doi: 10.1111/j.1469-1809.2009.00530.x. Epub 2009 Jul 1. Ann Hum Genet. 2009. PMID: 19573206 Free PMC article.

8

Array-based FMR1 sequencing and deletion analysis in patients with a fragile X syndrome-like phenotype.

Collins SC, Coffee B, Benke PJ, Berry-Kravis E, Gilbert F, Oostra B, Halley D, Zwick ME, Cutler DJ, Warren ST. Collins SC, et al. Among authors: zwick me. PLoS One. 2010 Mar 5;5(3):e9476. doi: 10.1371/journal.pone.0009476. PLoS One. 2010. PMID: 20221430 Free PMC article.

9

Empirical evaluation of oligonucleotide probe selection for DNA microarrays.

Mulle JG, Patel VC, Warren ST, Hegde MR, Cutler DJ, Zwick ME. Mulle JG, et al. Among authors: zwick me. PLoS One. 2010 Mar 29;5(3):e9921. doi: 10.1371/journal.pone.0009921. PLoS One. 2010. PMID: 20360966 Free PMC article.

10

Identification of novel FMR1 variants by massively parallel sequencing in developmentally delayed males.

Collins SC, Bray SM, Suhl JA, Cutler DJ, Coffee B, Zwick ME, Warren ST. Collins SC, et al. Among authors: zwick me. Am J Med Genet A. 2010 Oct;152A(10):2512-20. doi: 10.1002/ajmg.a.33626. Am J Med Genet A. 2010. PMID: 20799337 Free PMC article.

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