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Field
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postdoctoral research position is open in the LTS4 laboratory of EPFL in the context of the SATURNA research initiative, dedicated to decoding the dynamic choreography of RNA, and to understanding how
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positions in the professional ranks. Preferred Qualifications: Experience with protein expression and purification, and\or molecular microbiology (RNA-Seq, gene-knockout and mutation) Perks of Working at UNR
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feeding into the MNase-defined cistrome occupancy (MOA-seq) analysis of transcription factor binding of tomato promoter elements controlling the Zn and Fe deficiency responsive gene expression. You will
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lab techniques: classical diagnostic parasitology techniques, microscopy, parasite culture, in vitro assays, DNA and RNA extraction, PCR, RTPCR, qPCR, qRT-PCR, digital PCR, and ELISA. Experience with
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datasets, including scRNA-seq, scATAC-seq, scCUT&Tag, HiC, and proteomics, with an emphasis on trajectory inference, regulatory dynamics, and cell fate decisions. A key goal is to integrate multimodal data
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confocal microscopy ● Protein, RNA and DNA preparation, molecular cloning and purification of recombinant protein from e.coli, insect cells etc. and analyses; mammalian cell culture with sterile
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non-coding RNAs in the Nakanishi Lab (http://u.osu.edu/nakanishilab/ ). We are looking for a highly motivated scientist to join us in exploring the diverse roles of non-coding RNAs. Responsibilities
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, DNA/RNA extraction, Sanger and amplicon sequencing, and analysis of editing outcomes. Track record of first-author peer-reviewed publications. Strong written and oral communication in English, and the
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development, progression, metastasis, and prognosis. The Postdoc should have experience in processing and analyzing data from the next-generation sequencing and single-cell technologies (e.g., scRNA-seq
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. The team uses quantitative RNA measurements, immunohistochemistry and confocal imaging techniques, and is developing measurements using HPLC, enzymatic assays, and chemiluminescence. In-vivo human studies