You will get a predictive machine learning model (medical diagnosis,churn etc)

Project details
-Well-Commented code in python fro each step of the workflow
-Step by step instructions on how to update the model on new training data.
-Instructions on how to to obtain predictions for new data
-Unlimited Support through Upwork Messages
-Step by step instructions on how to update the model on new training data.
-Instructions on how to to obtain predictions for new data
-Unlimited Support through Upwork Messages
Machine Learning Tools
Azure Machine Learning, ChatGPT, Google AutoML, Google Data Studio, Google Sheets, H2O, Keras, KNIME, Microsoft Excel, Microsoft Power BI, Minitab, MLflow, NumPy, OpenCV, pandas, Python, Python Scikit-Learn, scikit-learn, SPSS, SQL, Stata, Tableau, TensorFlow, Word2vec, XGBoostWhat's included
| Service Tiers |
Starter
$800
|
Standard
$2,500
|
Advanced
$3,500
|
|---|---|---|---|
| Delivery Time | 20 days | 12 days | 1 day |
Number of Revisions | 2 | 3 | 4 |
Number of Model Variations | 1 | 2 | 3 |
Model Validation/Testing | |||
Model Documentation | |||
Data Source Connectivity | |||
Source Code |
Optional add-ons
You can add these on the next page.
Fast Delivery
+$400
APi
(+ 10 Days)
+$200
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About Robin
Bioinformatics Scientist | Cancer Genomics | Whole Exome Analysis
91%
Job Success
Delhi, India - 10:38 pm local time
🧬 About Me
Senior Bioinformatics Scientist at AIIMS Delhi with 5+ years of specialized experience in cancer genomics, NGS data analysis, and computational pipeline development. I translate complex genomic data into actionable biological insights for high-impact research and clinical applications.
Why Choose Me:
✅ Top-Rated Expert with proven track record in delivering publication-quality analyses
✅ Production-Ready Solutions - Scalable, reproducible pipelines deployed in clinical and research settings
✅ Academic Excellence - Active researcher at India's premier medical institution (AIIMS)
✅ End-to-End Expertise - From raw sequencing data to manuscript-ready figures
✅ Fast Turnaround - Efficient workflows optimized for HPC and cloud environments
🔬 Specialized Expertise
Cancer Genomics & Clinical Bioinformatics
Whole-Exome Sequencing (WES): Somatic mutation calling, CNV analysis, tumor evolution
Whole-Genome Sequencing (WGS): Structural variants, mutational signatures, driver gene identification
Multi-region tumor analysis: Clonal deconvolution, phylogenetic reconstruction, metastatic tracking
Clinical variant interpretation: ACMG guidelines, actionable biomarker identification
Transcriptomics & Single-Cell Analysis
Bulk RNA-seq: Differential expression, pathway enrichment, gene fusion detection
scRNA-seq: Cell type annotation, trajectory analysis, tumor microenvironment profiling
Multi-omics integration: ATAC-seq, ChIP-seq, spatial transcriptomics
Pipeline Development & Automation
Workflow Languages: Nextflow (DSL2), Snakemake, CWL
Containerization: Docker, Singularity for reproducible environments
Cloud & HPC: AWS (S3, EC2, Batch), GCP, SLURM clusters
CI/CD: Automated testing, version control, deployment pipelines
💻 Technical Stack
Programming & Analysis:
Python (Pandas, NumPy, Scanpy, Biopython) | R (Seurat, DESeq2, edgeR, ggplot2, Bioconductor) | Bash scripting
NGS Tools & Pipelines:
GATK | Mutect2 | VarScan2 | STAR | Kallisto | Salmon | Cell Ranger | FastQC | Picard | SAMtools | BWA | Bcftools
Variant Analysis:
VEP | ANNOVAR | SnpEff | CNVkit | FACETS | PyClone | SciClone
Machine Learning:
Scikit-learn | TensorFlow | Random Forests | Survival analysis | Predictive modeling
Visualization:
R Shiny | Plotly | ggplot2 | ComplexHeatmap | IGV | UCSC Genome Browser
DevOps & Collaboration:
Git/GitHub | Docker | CI/CD | Agile methodology | Technical documentation
📊 Services I Offer
🔹 Whole-Exome/Genome Analysis - Comprehensive variant calling, annotation, and clinical interpretation
🔹 Cancer Genomics - Tumor evolution, mutational signatures, clonal architecture
🔹 RNA-seq Analysis - Bulk and single-cell transcriptomics with biological interpretation
🔹 Pipeline Development - Custom, scalable Nextflow/Snakemake workflows
🔹 Multi-Omics Integration - Combined analysis of genomic, transcriptomic, and epigenomic data
🔹 Data Visualization - Publication-quality figures and interactive dashboards
🔹 Manuscript Preparation - Methods writing, results interpretation, figure generation
🔹 Consulting - Project design, tool selection, result interpretation
🎯 What You Can Expect
📈 Publication-Quality Work - Analyses meeting standards for top-tier journals
⚡ Efficient Delivery - Optimized workflows ensuring rapid turnaround
📝 Clear Communication - Regular updates, detailed documentation, comprehensive reports
🔄 Reproducible Research - Well-documented code, version-controlled pipelines
🤝 Collaborative Approach - Understanding your research goals and delivering tailored solutions
🏆 Project Highlights
✨ Multi-region tumor sequencing analysis for clonal evolution studies
✨ Clinical WES pipelines for pediatric cancer research at AIIMS
✨ Single-cell RNA-seq analysis for tumor microenvironment characterization
✨ Automated NGS pipelines processing 100+ samples with quality control
✨ Custom R Shiny dashboards for interactive data exploration
📬 Let's Collaborate
Whether you need comprehensive genomic analysis, custom pipeline development, or publication support, I bring the expertise and dedication to make your project a success.
Ready to transform your genomic data into breakthrough discoveries?
Let's discuss your project requirements today!
Available for: Long-term contracts | Short-term projects | Ongoing consultation
Response Time: Within 24 hours
Steps for completing your project
After purchasing the project, send requirements so Robin can start the project.
Delivery time starts when Robin receives requirements from you.
Robin works on your project following the steps below.
Revisions may occur after the delivery date.
Dataset
Model Accuracy