Nelson SF - Search Results

1

Resolving individuals contributing trace amounts of DNA to highly complex mixtures using high-density SNP genotyping microarrays.

Homer N, Szelinger S, Redman M, Duggan D, Tembe W, Muehling J, Pearson JV, Stephan DA, Nelson SF, Craig DW. Homer N, et al. Among authors: nelson sf. PLoS Genet. 2008 Aug 29;4(8):e1000167. doi: 10.1371/journal.pgen.1000167. PLoS Genet. 2008. PMID: 18769715 Free PMC article.

2

Multimarker analysis and imputation of multiple platform pooling-based genome-wide association studies.

Homer N, Tembe WD, Szelinger S, Redman M, Stephan DA, Pearson JV, Nelson SF, Craig D. Homer N, et al. Among authors: nelson sf. Bioinformatics. 2008 Sep 1;24(17):1896-902. doi: 10.1093/bioinformatics/btn333. Epub 2008 Jul 10. Bioinformatics. 2008. PMID: 18617537 Free PMC article.

3

Local alignment of two-base encoded DNA sequence.

Homer N, Merriman B, Nelson SF. Homer N, et al. Among authors: nelson sf. BMC Bioinformatics. 2009 Jun 9;10:175. doi: 10.1186/1471-2105-10-175. BMC Bioinformatics. 2009. PMID: 19508732 Free PMC article.

4

BFAST: an alignment tool for large scale genome resequencing.

Homer N, Merriman B, Nelson SF. Homer N, et al. Among authors: nelson sf. PLoS One. 2009 Nov 11;4(11):e7767. doi: 10.1371/journal.pone.0007767. PLoS One. 2009. PMID: 19907642 Free PMC article.

5

Improving the efficiency of genomic loci capture using oligonucleotide arrays for high throughput resequencing.

Lee H, O'Connor BD, Merriman B, Funari VA, Homer N, Chen Z, Cohn DH, Nelson SF. Lee H, et al. Among authors: nelson sf. BMC Genomics. 2009 Dec 31;10:646. doi: 10.1186/1471-2164-10-646. BMC Genomics. 2009. PMID: 20043857 Free PMC article.

6

U87MG decoded: the genomic sequence of a cytogenetically aberrant human cancer cell line.

Clark MJ, Homer N, O'Connor BD, Chen Z, Eskin A, Lee H, Merriman B, Nelson SF. Clark MJ, et al. Among authors: nelson sf. PLoS Genet. 2010 Jan 29;6(1):e1000832. doi: 10.1371/journal.pgen.1000832. PLoS Genet. 2010. PMID: 20126413 Free PMC article.

7

Local alignment of generalized k-base encoded DNA sequence.

Homer N, Nelson SF, Merriman B. Homer N, et al. Among authors: nelson sf. BMC Bioinformatics. 2010 Jun 24;11:347. doi: 10.1186/1471-2105-11-347. BMC Bioinformatics. 2010. PMID: 20576157 Free PMC article.

8

Improved variant discovery through local re-alignment of short-read next-generation sequencing data using SRMA.

Homer N, Nelson SF. Homer N, et al. Among authors: nelson sf. Genome Biol. 2010;11(10):R99. doi: 10.1186/gb-2010-11-10-r99. Epub 2010 Oct 8. Genome Biol. 2010. PMID: 20932289 Free PMC article.

9

Correction: U87MG Decoded: The Genomic Sequence of a Cytogenetically Aberrant Human Cancer Cell Line.

Clark MJ, Homer N, O'Connor BD, Chen Z, Eskin A, Lee H, Merriman B, Nelson SF. Clark MJ, et al. Among authors: nelson sf. PLoS Genet. 2018 May 16;14(5):e1007392. doi: 10.1371/journal.pgen.1007392. eCollection 2018 May. PLoS Genet. 2018. PMID: 29768410 Free PMC article.

10

Congenital myasthenic syndrome caused by a frameshift insertion mutation in GFPT1.

Szelinger S, Krate J, Ramsey K, Strom SP, Shieh PB, Lee H, Belnap N, Balak C, Siniard AL, Russell M, Richholt R, Both M, Claasen AM, Schrauwen I, Nelson SF, Huentelman MJ, Craig DW, Yang SP, Moore SA, Sivakumar K, Narayanan V, Rangasamy S; UCLA Clinical Genomics Center. Szelinger S, et al. Among authors: nelson sf. Neurol Genet. 2020 Jun 30;6(4):e468. doi: 10.1212/NXG.0000000000000468. eCollection 2020 Aug. Neurol Genet. 2020. PMID: 32754643 Free PMC article.

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