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Items: 4

1.

Precise detection of de novo single nucleotide variants in human genomes.

Gómez-Romero L, Palacios-Flores K, Reyes J, García D, Boege M, Dávila G, Flores M, Schatz MC, Palacios R.

Proc Natl Acad Sci U S A. 2018 May 22;115(21):5516-5521. doi: 10.1073/pnas.1802244115. Epub 2018 May 7.

2.

A Perfect Match Genomic Landscape Provides a Unified Framework for the Precise Detection of Variation in Natural and Synthetic Haploid Genomes.

Palacios-Flores K, García-Sotelo J, Castillo A, Uribe C, Aguilar L, Morales L, Gómez-Romero L, Reyes J, Garciarubio A, Boege M, Dávila G.

Genetics. 2018 Apr;208(4):1631-1641. doi: 10.1534/genetics.117.300589. Epub 2018 Jan 24.

3.

Assessing noise sources at synchrotron infrared ports.

Lerch P, Dumas P, Schilcher T, Nadji A, Luedeke A, Hubert N, Cassinari L, Boege M, Denard JC, Stingelin L, Nadolski L, Garvey T, Albert S, Gough Ch, Quack M, Wambach J, Dehler M, Filhol JM.

J Synchrotron Radiat. 2012 Jan;19(Pt 1):1-9. doi: 10.1107/S0909049511041884. Epub 2011 Nov 25.

4.

Context-dependent individualization of nucleotides and virtual genomic hybridization allow the precise location of human SNPs.

Reyes J, Gómez-Romero L, Ibarra-Soria X, Palacios-Flores K, Arriola LR, Wences A, García D, Boege M, Dávila G, Flores M, Palacios R.

Proc Natl Acad Sci U S A. 2011 Sep 13;108(37):15294-9. doi: 10.1073/pnas.1112567108. Epub 2011 Aug 29.

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