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Methods in Molecular Biology (Clifton, N.J.)
|
December 20, 2002
Nanoelectrospray tandem mass spectrometry and sequence similarity searching for identification of proteins from organisms with unknown genomes
Anna Shevchenko, Shamil Sunyaev, Adam Liska, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 2, 2018
A literature review at genome scale: improving clinical variant assessment
Christopher A Cassa, Daniel M Jordan, Ivan Adzhubei, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 7, 2009
Triplet repeat length bias and variation in the human transcriptome
Michael Molla, Arthur Delcher, Shamil Sunyaev, et al.
American Journal of Human Genetics
|
December 24, 2021
Overcoming constraints on the detection of recessive selection in human genes from population frequency data
Daniel J Balick, Daniel M Jordan, Shamil Sunyaev, et al.
Analytical Chemistry
|
March 28, 2003
MultiTag: multiple error-tolerant sequence tag search for the sequence-similarity identification of proteins by mass spectrometry
Shamil Sunyaev, Adam J Liska, Alexander Golod, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 29, 2026
Incorporation of Clinical and Molecular Variant Properties Improves the Performance of in silico Pathogenicity Prediction Tools
Ofer Isakov, Reut Fluss, Dina Marek-Yagel, et al.
Nature Genetics
|
January 13, 2015
No evidence that selection has been less effective at removing deleterious mutations in Europeans than in Africans
Ron Do, Daniel Balick, Heng Li, et al.
Proteomics
|
August 27, 2005
Error-tolerant EST database searches by tandem mass spectrometry and multiTag software
Adam J Liska, Shamil Sunyaev, Ignat N Shilov, et al.
Bioinformatics (Oxford, England)
|
September 1, 2018
novoCaller: a Bayesian network approach for de novo variant calling from pedigree and population sequence data
Anwoy Kumar Mohanty, Dana Vuzman, Laurent Francioli, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
October 30, 2008
SNP2RFLP: a computational tool to facilitate genetic mapping using benchtop analysis of SNPs
Wesley A Beckstead, Bryan C Bjork, Rolf W Stottmann, et al.
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Search research articles
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Showing results (21-30 of 75) with videos related to
Sort By:
Page
of 8
Methods in Molecular Biology (Clifton, N.J.)
|
December 20, 2002
Nanoelectrospray tandem mass spectrometry and sequence similarity searching for identification of proteins from organisms with unknown genomes
Anna Shevchenko, Shamil Sunyaev, Adam Liska, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 2, 2018
A literature review at genome scale: improving clinical variant assessment
Christopher A Cassa, Daniel M Jordan, Ivan Adzhubei, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 7, 2009
Triplet repeat length bias and variation in the human transcriptome
Michael Molla, Arthur Delcher, Shamil Sunyaev, et al.
American Journal of Human Genetics
|
December 24, 2021
Overcoming constraints on the detection of recessive selection in human genes from population frequency data
Daniel J Balick, Daniel M Jordan, Shamil Sunyaev, et al.
Analytical Chemistry
|
March 28, 2003
MultiTag: multiple error-tolerant sequence tag search for the sequence-similarity identification of proteins by mass spectrometry
Shamil Sunyaev, Adam J Liska, Alexander Golod, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 29, 2026
Incorporation of Clinical and Molecular Variant Properties Improves the Performance of in silico Pathogenicity Prediction Tools
Ofer Isakov, Reut Fluss, Dina Marek-Yagel, et al.
Nature Genetics
|
January 13, 2015
No evidence that selection has been less effective at removing deleterious mutations in Europeans than in Africans
Ron Do, Daniel Balick, Heng Li, et al.
Proteomics
|
August 27, 2005
Error-tolerant EST database searches by tandem mass spectrometry and multiTag software
Adam J Liska, Shamil Sunyaev, Ignat N Shilov, et al.
Bioinformatics (Oxford, England)
|
September 1, 2018
novoCaller: a Bayesian network approach for de novo variant calling from pedigree and population sequence data
Anwoy Kumar Mohanty, Dana Vuzman, Laurent Francioli, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
October 30, 2008
SNP2RFLP: a computational tool to facilitate genetic mapping using benchtop analysis of SNPs
Wesley A Beckstead, Bryan C Bjork, Rolf W Stottmann, et al.
Page
of 8