M
Michael Snyder
Researcher at Stanford University
Publications - 938
Citations - 150929
Michael Snyder is an academic researcher from Stanford University. The author has contributed to research in topics: Gene & Genome. The author has an hindex of 169, co-authored 840 publications receiving 130225 citations. Previous affiliations of Michael Snyder include Wyss Institute for Biologically Inspired Engineering & Public Health Research Institute.
Papers
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Journal ArticleDOI
A dynamic approach to mapping coordinates between microplates and microarrays
Kei-Hoi Cheung,Janet Hager,Kenneth Nelson,Kevin P. White,Yuli Li,Michael Snyder,Kenneth R. Williams,Perry L. Miller +7 more
TL;DR: A general algorithm that correlates the well positions of DNA samples in each microplate to the positions of the spots on each array slide is described and a flexible and platform-independent program named MicroArray Convolutor (MAC) is implemented.
Posted ContentDOI
NF90/ILF3 is a transcription factor that promotes proliferation over differentiation by hierarchical regulation in K562 erythroleukemia cells
Ting-Hsuan Wu,Lingfang Shi,Jessika Adrian,Minyi Shi,Ramesh V. Nair,Michael Snyder,Peter N. Kao +6 more
TL;DR: ENCODE ChIP-seq identified 9,081 genomic sites specifically bound by NF90/110 in K562 cells and revealed that NF90 directly activates transcription factors that drive growth and proliferation (EGR1, MYC), while attenuating differentiation along erythroid lineage (KLF1).
Posted ContentDOI
Evolution of diapause in the African turquoise killifish by remodeling ancient gene regulatory landscape
Param Priya Singh,G. Adam Reeves,Kévin Contrepois,Kévin Contrepois,Mathew Ellenberger,Chi-Kuo Hu,Michael Snyder,Michael Snyder,Anne Brunet +8 more
TL;DR: In this paper, the African turquoise killifish has evolved diapause as a form of suspended development to survive the complete drought that occurs every year in its habitat.
Journal ArticleDOI
Analyzing In Vivo Metabolite‐Protein Interactions by Large‐Scale Systematic Analyses
Xiyan Li,Michael Snyder +1 more
TL;DR: This procedure couples protein affinity purification and mass spectrometry to identify metabolite‐protein interactions in vivo and can be completed within 1 day and scaled to process hundreds of samples in a batch.
Book ChapterDOI
Global analysis of transcription factor-binding sites in yeast using ChIP-Seq.
TL;DR: This chapter describes a ChIP-Seq strategy adapted for budding yeast to enable the genome-wide characterization of binding sites of transcription factors (TFs) and other DNA-binding proteins in an efficient and cost-effective way.