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BMC Medical Genomics
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June 18, 2015
High-resolution characterization of sequence signatures due to non-random cleavage of cell-free DNA
Dineika Chandrananda, Natalie P Thorne, Melanie Bahlo
Briefings in Bioinformatics
|
November 3, 2016
Evaluation of computational programs to predict HLA genotypes from genomic sequencing data
Denis C Bauer, Armella Zadoorian, Laurence O W Wilson, et al.
BMC Genomics
|
October 8, 2010
The cost of reducing starting RNA quantity for Illumina BeadArrays: a bead-level dilution experiment
Andy G Lynch, James Hadfield, Mark J Dunning, et al.
BMC Bioinformatics
|
January 27, 2007
Missing channels in two-colour microarray experiments: combining single-channel and two-channel data
Andy G Lynch, David E Neal, John D Kelly, et al.
Plos One
|
July 12, 2014
Harnessing gene expression networks to prioritize candidate epileptic encephalopathy genes
Karen L Oliver, Vesna Lukic, Natalie P Thorne, et al.
Plos One
|
February 4, 2014
Investigating and correcting plasma DNA sequencing coverage bias to enhance aneuploidy discovery
Dineika Chandrananda, Natalie P Thorne, Devika Ganesamoorthy, et al.
Nucleic Acids Research
|
July 26, 2008
Tissue-specific splicing factor gene expression signatures
Ana Rita Grosso, Anita Q Gomes, Nuno L Barbosa-Morais, et al.
Cell Cycle (Georgetown, Tex.)
|
November 13, 2008
AURKA overexpression accompanies dysregulation of DNA-damage response genes in invasive urothelial cell carcinoma
Abhi Veerakumarasivam, Leonard D Goldstein, Kasra Saeb-Parsy, et al.
Nucleic Acids Research
|
October 17, 2006
MMASS: an optimized array-based method for assessing CpG island methylation
Ashraf E K Ibrahim, Natalie P Thorne, Katie Baird, et al.
Cancer Research
|
August 4, 2006
Metabolic consequences of p300 gene deletion in human colon cancer cells
Jacob G Bundy, N Gopalakrishna Iyer, Michelle S Gentile, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 20) with videos related to
Sort By:
Page
of 2
BMC Medical Genomics
|
June 18, 2015
High-resolution characterization of sequence signatures due to non-random cleavage of cell-free DNA
Dineika Chandrananda, Natalie P Thorne, Melanie Bahlo
Briefings in Bioinformatics
|
November 3, 2016
Evaluation of computational programs to predict HLA genotypes from genomic sequencing data
Denis C Bauer, Armella Zadoorian, Laurence O W Wilson, et al.
BMC Genomics
|
October 8, 2010
The cost of reducing starting RNA quantity for Illumina BeadArrays: a bead-level dilution experiment
Andy G Lynch, James Hadfield, Mark J Dunning, et al.
BMC Bioinformatics
|
January 27, 2007
Missing channels in two-colour microarray experiments: combining single-channel and two-channel data
Andy G Lynch, David E Neal, John D Kelly, et al.
Plos One
|
July 12, 2014
Harnessing gene expression networks to prioritize candidate epileptic encephalopathy genes
Karen L Oliver, Vesna Lukic, Natalie P Thorne, et al.
Plos One
|
February 4, 2014
Investigating and correcting plasma DNA sequencing coverage bias to enhance aneuploidy discovery
Dineika Chandrananda, Natalie P Thorne, Devika Ganesamoorthy, et al.
Nucleic Acids Research
|
July 26, 2008
Tissue-specific splicing factor gene expression signatures
Ana Rita Grosso, Anita Q Gomes, Nuno L Barbosa-Morais, et al.
Cell Cycle (Georgetown, Tex.)
|
November 13, 2008
AURKA overexpression accompanies dysregulation of DNA-damage response genes in invasive urothelial cell carcinoma
Abhi Veerakumarasivam, Leonard D Goldstein, Kasra Saeb-Parsy, et al.
Nucleic Acids Research
|
October 17, 2006
MMASS: an optimized array-based method for assessing CpG island methylation
Ashraf E K Ibrahim, Natalie P Thorne, Katie Baird, et al.
Cancer Research
|
August 4, 2006
Metabolic consequences of p300 gene deletion in human colon cancer cells
Jacob G Bundy, N Gopalakrishna Iyer, Michelle S Gentile, et al.
Page
of 2