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Medical School-affiliated hospitals. Requirements The postdoctoral fellow will perform computational analyses of novel single-cell epigenomic datasets (incl. DNA methylation) generated from different
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The University of Texas MD Anderson Cancer Center | Houston, Texas | United States | about 18 hours ago
), combined DNA methylation and genomic alterations in lung cancer evolution (Gimeno-Valiente et al., Nature Genetics 2025), benchmarking methods for subclonal reconstruction (Salcedo et al., Nature
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Cancer Gene Panel assay, a molecular test profiling DNA from tumor and normal tissue to identify mutations that may drive a patient’s cancer and aid in diagnosis and treatment, and a related RNAseq
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and optimizing algorithms. Lab experience analyzing DTI / DSI brain tractography in DS vs Normals. Analyzing 7 intercellular databases ( DNA Methylation, RNA -seq, miRNA, Protein, Phosphoprotein
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research strategy. 2. Undertake laboratory-based analyses and perform molecular biology techniques including nucleic acid extraction, gene expression analyses, histological assessments and DNA methylation
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/sample preparation for RNA-seq, ATAC-seq and DNA methylation analyses Coordinate genomic, transcriptomic, lipidomic, metabolomic analyses with our internal and external collaborating laboratories and take
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types of omics data from high throughput technologies such as single-cell, bulk and spatial RNA-seq, ChIP-seq, CUT&RUN, DNA methylation, eQTL mapping, and immune repertoire sequencing, both in
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publications and grant applications. The Fellow may contribute to projects involving: multi-omics analyses (single-cell, cell-free RNA/DNA, methylation, proteomics); biomarker discovery for pregnancy
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, RNA -seq, and DNA methylation data. Develop and implement state-of-the-art computational and statistical methods for integrative analysis of multi-omics datasets. Utilize high-performance computing
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Diagnostic Laboratory of Dr. Arupa Ganguly. You will perform routine and complex laboratory techniques/procedures including, but not exclusive, all aspects of DNA isolation, mutation detection in human