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Automating sequence-based detection and genotyping of SNPs from diploid samples

autor

Deborah A Nickerson

1954 - 2021

publicado en: Nature Genetics

fecha de publicación: 2006-02-19

idioma: inglés

tema principal: automatización

Cites articles 15

Fecha

Título

Autores

2005-03-01

novoSNP, a novel computational tool for sequence variation discovery

Christine Van Broeckhoven, Peter De Rijk, Rosa Rademakers
2005-02-01

Whole-genome patterns of common DNA variation in three human populations

David A Hinds, Kelly A. Frazer
2005-10-27

A haplotype map of the human genome
2004-11-03

Comprehensive identification and characterization of diallelic insertion-deletion polymorphisms in 330 human candidate genes

Deborah A Nickerson
2003-03-24

Additional SNPs and linkage-disequilibrium analyses are necessary for whole-genome association studies in humans

Deborah A Nickerson, Leonid Kruglyak
2001-02-01

SNPing in the human genome
2001-10

SSAHA: a fast search method for large DNA databases
2000-11-01

Environmental health and genomics: visions and implications
1999-07

Characterization of single-nucleotide polymorphisms in coding regions of human genes

David Altshuler, Kristin Ardlie, Eric Lander
1999-12-01

A general approach to single-nucleotide polymorphism discovery.

Pui-Yan Kwok
1998-03

Base-calling of automated sequencer traces using phred. II. Error probabilities
1998-03

Base-calling of automated sequencer traces using phred. I. Accuracy assessment
1998-03

Consed: a graphical tool for sequence finishing
1997-07-15

PolyPhred: automating the detection and genotyping of single nucleotide substitutions using fluorescence-based resequencing
1994-09

Comparative Analysis of Human DNA Variations by Fluorescence-Based Sequencing of PCR Products

Pui-Yan Kwok

Artículo - wd:Q36403396

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