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Sajani Swamy

Showing results (1-10 of 8) with videos related to

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Molecular & Cellular Proteomics : MCP|January 25, 2008
Comparison of Mascot and X!Tandem performance for low and high accuracy mass spectrometry and the development of an adjusted Mascot thresholdMarkus Brosch, Sajani Swamy, Tim Hubbard, et al.
Bioinformatics (Oxford, England)|May 15, 2012
Strelka: accurate somatic small-variant calling from sequenced tumor-normal sample pairsChristopher T Saunders, Wendy S W Wong, Sajani Swamy, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 20, 2013
Whole-genome haplotyping by dilution, amplification, and sequencingFiona Kaper, Sajani Swamy, Brandy Klotzle, et al.
RNA (New York, N.Y.)|May 24, 2013
Thermostable group II intron reverse transcriptase fusion proteins and their use in cDNA synthesis and next-generation RNA sequencingSabine Mohr, Eman Ghanem, Whitney Smith, et al.
Biostatistics (Oxford, England)|October 20, 2009
PICNIC: an algorithm to predict absolute allelic copy number variation with microarray cancer dataChris D Greenman, Graham Bignell, Adam Butler, et al.
Science Signaling|April 30, 2009
Neurotransmitters drive combinatorial multistate postsynaptic density networksMarcelo P Coba, Andrew J Pocklington, Mark O Collins, et al.
Nature|February 19, 2010
Signatures of mutation and selection in the cancer genomeGraham R Bignell, Chris D Greenman, Helen Davies, et al.
Molecular Genetics & Genomic Medicine|October 17, 2022
Scalable detection of technically challenging variants through modified next-generation sequencingSusan Rojahn, Tina Hambuch, Jessika Adrian, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Molecular & Cellular Proteomics : MCP|January 25, 2008
Comparison of Mascot and X!Tandem performance for low and high accuracy mass spectrometry and the development of an adjusted Mascot thresholdMarkus Brosch, Sajani Swamy, Tim Hubbard, et al.
Bioinformatics (Oxford, England)|May 15, 2012
Strelka: accurate somatic small-variant calling from sequenced tumor-normal sample pairsChristopher T Saunders, Wendy S W Wong, Sajani Swamy, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 20, 2013
Whole-genome haplotyping by dilution, amplification, and sequencingFiona Kaper, Sajani Swamy, Brandy Klotzle, et al.
RNA (New York, N.Y.)|May 24, 2013
Thermostable group II intron reverse transcriptase fusion proteins and their use in cDNA synthesis and next-generation RNA sequencingSabine Mohr, Eman Ghanem, Whitney Smith, et al.
Biostatistics (Oxford, England)|October 20, 2009
PICNIC: an algorithm to predict absolute allelic copy number variation with microarray cancer dataChris D Greenman, Graham Bignell, Adam Butler, et al.
Science Signaling|April 30, 2009
Neurotransmitters drive combinatorial multistate postsynaptic density networksMarcelo P Coba, Andrew J Pocklington, Mark O Collins, et al.
Nature|February 19, 2010
Signatures of mutation and selection in the cancer genomeGraham R Bignell, Chris D Greenman, Helen Davies, et al.
Molecular Genetics & Genomic Medicine|October 17, 2022
Scalable detection of technically challenging variants through modified next-generation sequencingSusan Rojahn, Tina Hambuch, Jessika Adrian, et al.
Pageof 1