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Plos Genetics
|
September 13, 2006
Allele frequency matching between SNPs reveals an excess of linkage disequilibrium in genic regions of the human genome
Michael A Eberle, Mark J Rieder, Leonid Kruglyak, et al.
Nature
|
May 28, 2004
Mapping complex disease loci in whole-genome association studies
Christopher S Carlson, Michael A Eberle, Leonid Kruglyak, et al.
Bioinformatics (Oxford, England)
|
October 23, 2009
Targeted interrogation of copy number variation using SCIMMkit
Troy Zerr, Gregory M Cooper, Evan E Eichler, et al.
Human Molecular Genetics
|
September 18, 2010
Massively parallel sequencing and rare disease
Sarah B Ng, Deborah A Nickerson, Michael J Bamshad, et al.
Drug Metabolism Reviews
|
May 9, 2008
The environmental genome project: reference polymorphisms for drug metabolism genes and genome-wide association studies
Mark J Rieder, Robert J Livingston, Ian B Stanaway, et al.
Human Molecular Genetics
|
November 5, 2004
Comprehensive identification and characterization of diallelic insertion-deletion polymorphisms in 330 human candidate genes
Tushar R Bhangale, Mark J Rieder, Robert J Livingston, et al.
Clinical Pharmacology and Therapeutics
|
June 18, 2019
Calling Star Alleles With Stargazer in 28 Pharmacogenes With Whole Genome Sequences
Seung-Been Lee, Marsha M Wheeler, Kenneth E Thummel, et al.
Human Genetics
|
May 9, 2006
Efficient selection of tagging single-nucleotide polymorphisms in multiple populations
Bryan N Howie, Christopher S Carlson, Mark J Rieder, et al.
Nature Methods
|
April 8, 2009
Massively parallel exon capture and library-free resequencing across 16 genomes
Emily H Turner, Choli Lee, Sarah B Ng, et al.
Nature Genetics
|
February 24, 2006
Automating sequence-based detection and genotyping of SNPs from diploid samples
Matthew Stephens, James S Sloan, P D Robertson, et al.
Page
of 38
Search research articles
Search
Showing results (11-20 of 380) with videos related to
Sort By:
Page
of 38
Plos Genetics
|
September 13, 2006
Allele frequency matching between SNPs reveals an excess of linkage disequilibrium in genic regions of the human genome
Michael A Eberle, Mark J Rieder, Leonid Kruglyak, et al.
Nature
|
May 28, 2004
Mapping complex disease loci in whole-genome association studies
Christopher S Carlson, Michael A Eberle, Leonid Kruglyak, et al.
Bioinformatics (Oxford, England)
|
October 23, 2009
Targeted interrogation of copy number variation using SCIMMkit
Troy Zerr, Gregory M Cooper, Evan E Eichler, et al.
Human Molecular Genetics
|
September 18, 2010
Massively parallel sequencing and rare disease
Sarah B Ng, Deborah A Nickerson, Michael J Bamshad, et al.
Drug Metabolism Reviews
|
May 9, 2008
The environmental genome project: reference polymorphisms for drug metabolism genes and genome-wide association studies
Mark J Rieder, Robert J Livingston, Ian B Stanaway, et al.
Human Molecular Genetics
|
November 5, 2004
Comprehensive identification and characterization of diallelic insertion-deletion polymorphisms in 330 human candidate genes
Tushar R Bhangale, Mark J Rieder, Robert J Livingston, et al.
Clinical Pharmacology and Therapeutics
|
June 18, 2019
Calling Star Alleles With Stargazer in 28 Pharmacogenes With Whole Genome Sequences
Seung-Been Lee, Marsha M Wheeler, Kenneth E Thummel, et al.
Human Genetics
|
May 9, 2006
Efficient selection of tagging single-nucleotide polymorphisms in multiple populations
Bryan N Howie, Christopher S Carlson, Mark J Rieder, et al.
Nature Methods
|
April 8, 2009
Massively parallel exon capture and library-free resequencing across 16 genomes
Emily H Turner, Choli Lee, Sarah B Ng, et al.
Nature Genetics
|
February 24, 2006
Automating sequence-based detection and genotyping of SNPs from diploid samples
Matthew Stephens, James S Sloan, P D Robertson, et al.
Page
of 38