Computational Scientist I, Single-cell/Spatial Cancer Genomics, CGR
Frederick National Laboratory for Cancer Research · Rockville, MD · 1 wk ago
AnalystFull-time
Key Roles/Responsibilities
- Lead end-to-end analyses and discussions of single-cell, multiomics, spatial transcriptomics, and proteomics projects through close collaboration with DCEG investigators, CGR wet-lab scientists, MDPL scientists, and bioinformaticians.
- Demonstrate strong knowledge in experimental design, hypothesis formulation and sing, and development of analytical aims, leveraging expertise in cancer biology and spatial omics.
- Evaluate existing spatial infrastructure and analytical capabilities and build upon them by implementing state-of-the-art methods for single-cell RNA-seq, single-cell ATAC-seq, multi-omics, and spatial omics analyses.
- Use strong knowledge of community standards and best practices to benchmark existing and emerging software tools and incorporate them into workflows.
- Perform nuclear segmentation and expansion of high-resolution images by comparing various tools and optimize for different tissue and cancer types.
- Evaluate QC metrics and appropriate filtering criteria for downstream processing.
- Perform batch correction, data integration, cell clustering, and annotation.
- Identify and create new single-cell references across different cancer and tissue types.
- Study tumor microenvironments and immune cell infiltration.
- Apply statistical, machine learning, and deep learning approaches required for both upstream and downstream analyses.
- Develop clear, interpretable visualizations and analytical reports to communicate findings and support scientific discovery.
- Conduct reproducible scientific research through documentation of software versions, processes, and pipelines, along with the use of tools such as Markdown documents, Conda and R environments, Docker, Singularity, GitHub, and Snakemake/Nextflow.
- Use High-Performance Compute Clusters and the Slurm scheduler, optimize computational resources and data storage requirements to ensure scalability for large datasets.
- Summarize and interpret findings through clear visualizations and reports, and present results to senior leadership and scientists from diverse backgrounds.
- Contribute to manuscript preparation, submission, and revision processes, with strong opportunities for scientific co-authorship.
- Stay current with advances in the field through scientific literature review, seminars, workshops, and cross-disciplinary collaborations.
Basic Qualifications
- Possession of a PhD degree from an accredited college or university according to the Council for Higher Education Accreditation (CHEA) in Bioinformatics, Computational Biology, Biostatistics, or a related field. Foreign degrees must be evaluated for U.S. equivalency.
- Demonstrated experience with single-cell, single-nucleus multiomic, and spatial omics data analysis, including a solid understanding of statistical and analytical methods for biomarker discovery and spatial profiling.
- Experience working with both sequencing- and imaging-based spatial omics platforms.
- Strong publication record demonstrating the ability to analyze and interpret single-cell and spatial omics datasets.
- Strong programming skills in R and Python, with the ability to work in RStudio, VS Code, and Jupyter Notebooks.
- Strong knowledge of reproducibility practices and version control using Docker, Singularity, GitHub, workflow management systems (Snakemake/Nextflow), R and Conda environments, and Markdown documents.
- Proficiency in shell scripting (e.g., Bash, AWK, SED).
- Proficiency working in Linux-based HPC or cloud environments, with a strong understanding of Slurm and the ability to work with large datasets using best practices for algorithmic efficiency, parallelization, and scalability.
- Ability to work independently and collaboratively with internal and external investigators.
- Strong written, verbal, and presentation skills. Ability to work effectively in a multidisciplinary research environment and communicate technical findings clearly to non-specialist audiences through reports and presentations detailing methodologies and results.
- Efficient and organized data management for large projects.
- Strong work ethic and a proactive, solution-oriented mindset.
- Self-motivated, research-focused professional with a passion for advancing cancer genomics.
- Able to obtain and maintain a security clearance.
Preferred Qualifications
- Minimum of three years of postdoctoral or equivalent experience in academia or industry.
- Experience analyzing data from major single-cell and spatial platforms, including 10x Visium HD, Xenium, and Ultivue.
- Strong working knowledge of end-to-end processing and analysis of single-cell RNA-seq, single-cell ATAC-seq, single-nucleus multiomics, and spatial transcriptomics datasets.
- Proficiency in Cell Ranger, Space Ranger, StarDist, QuPath, and familiarity with HALO for evaluating tissue and data quality, nuclear segmentation, and image analysis.
- Familiarity with nuclear segmentation approaches such as CellPose, Baysor and Proseg, and cell-free spatial segmentation approaches such as FICTURE.
- Proficiency in Seurat, Bioconductor, SpatialData, Scanpy, and Squidpy frameworks for end-to-end analysis.
- Strong knowledge of:
- Harmony, FastMNN, and RPCA for batch correction
- Non-spatial (Leiden, Louvain) and spatial (Banksy, spaGCN) clustering algorithms
- RCTD, Azimuth, and SingleR for label transfer and cell annotation
- Cell-cell communication tools such as LIANA, CellChat, and CellPhoneDB
- DESeq2 for differential expression analysis
- Niche and pathway enrichment analysis (GSEA)
- Visualization tools such as Loupe Browser, IGV, and UCSC Genome Browser
- Major file formats such as BAM and Parquet
- Proficiency in creating high-quality visualizations using ggplot2 in R and data visualization libraries in Python (e.g., Matplotlib, Seaborn, Plotly).
- A public code portfolio (e.g., GitHub, GitLab) demonstrating relevant expertise.
- Additional experience analyzing bulk transcriptomics, proteomics, metabolomics, or cancer genomics data from next-generation sequencing platforms is a plus.