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Subramanian S Ajay

Showing results (1-10 of 15) with videos related to

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BMC Genomics|March 9, 2010
Unified translation repression mechanism for microRNAs and upstream AUGsSubramanian S Ajay, Brian D Athey, Inhan Lee
Genome Research|June 12, 2012
Genome-wide DNA methylation profiles in hematopoietic stem and progenitor cells reveal overrepresentation of ETS transcription factor binding sitesAmber Hogart, Jens Lichtenberg, Subramanian S Ajay, et al.
Plos One|August 23, 2011
A bioinformatics approach for determining sample identity from different lanes of high-throughput sequencing dataRachel L Goldfeder, Stephen C J Parker, Subramanian S Ajay, et al.
Nucleic Acids Research|January 23, 2008
Discriminating single-base difference miRNA expressions using microarray Probe Design Guru (ProDeG)Inhan Lee, Subramanian S Ajay, Haiming Chen, et al.
Genome Research|July 21, 2011
Accurate and comprehensive sequencing of personal genomesSubramanian S Ajay, Stephen C J Parker, Hatice Ozel Abaan, et al.
Genome Research|April 2, 2009
New class of microRNA targets containing simultaneous 5'-UTR and 3'-UTR interaction sitesInhan Lee, Subramanian S Ajay, Jong In Yook, et al.
Blood|September 9, 2011
Genome-wide ChIP-Seq reveals a dramatic shift in the binding of the transcription factor erythroid Kruppel-like factor during erythrocyte differentiationAndre M Pilon, Subramanian S Ajay, Swathi Ashok Kumar, et al.
NPJ Genomic Medicine|February 23, 2019
Clinical whole genome sequencing as a first-tier test at a resource-limited dysmorphology clinic in MexicoAlicia Scocchia, Kristen M Wigby, Diane Masser-Frye, et al.
Plos Genetics|August 23, 2012
Mutational signatures of de-differentiation in functional non-coding regions of melanoma genomesStephen C J Parker, Jared Gartner, Isabel Cardenas-Navia, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 9, 2018
Copy-number variants in clinical genome sequencing: deployment and interpretation for rare and undiagnosed diseaseAndrew M Gross, Subramanian S Ajay, Vani Rajan, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
BMC Genomics|March 9, 2010
Unified translation repression mechanism for microRNAs and upstream AUGsSubramanian S Ajay, Brian D Athey, Inhan Lee
Genome Research|June 12, 2012
Genome-wide DNA methylation profiles in hematopoietic stem and progenitor cells reveal overrepresentation of ETS transcription factor binding sitesAmber Hogart, Jens Lichtenberg, Subramanian S Ajay, et al.
Plos One|August 23, 2011
A bioinformatics approach for determining sample identity from different lanes of high-throughput sequencing dataRachel L Goldfeder, Stephen C J Parker, Subramanian S Ajay, et al.
Nucleic Acids Research|January 23, 2008
Discriminating single-base difference miRNA expressions using microarray Probe Design Guru (ProDeG)Inhan Lee, Subramanian S Ajay, Haiming Chen, et al.
Genome Research|July 21, 2011
Accurate and comprehensive sequencing of personal genomesSubramanian S Ajay, Stephen C J Parker, Hatice Ozel Abaan, et al.
Genome Research|April 2, 2009
New class of microRNA targets containing simultaneous 5'-UTR and 3'-UTR interaction sitesInhan Lee, Subramanian S Ajay, Jong In Yook, et al.
Blood|September 9, 2011
Genome-wide ChIP-Seq reveals a dramatic shift in the binding of the transcription factor erythroid Kruppel-like factor during erythrocyte differentiationAndre M Pilon, Subramanian S Ajay, Swathi Ashok Kumar, et al.
NPJ Genomic Medicine|February 23, 2019
Clinical whole genome sequencing as a first-tier test at a resource-limited dysmorphology clinic in MexicoAlicia Scocchia, Kristen M Wigby, Diane Masser-Frye, et al.
Plos Genetics|August 23, 2012
Mutational signatures of de-differentiation in functional non-coding regions of melanoma genomesStephen C J Parker, Jared Gartner, Isabel Cardenas-Navia, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 9, 2018
Copy-number variants in clinical genome sequencing: deployment and interpretation for rare and undiagnosed diseaseAndrew M Gross, Subramanian S Ajay, Vani Rajan, et al.
Pageof 2