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Biomedical Publication Projects | NTHRYS | Industry Oriented

Biomedical publication projects help you turn research into publishable papers—study design, data analysis, writing, figures, journal selection, and submission support—so your work meets ethical, statistical, and reporting standards.

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Biomedical Publication Projects

Biomedical publication projects help you turn research into publishable papers—study design, data analysis, writing, figures, journal selection, and submission support—so your work meets ethical, statistical, and reporting standards.

Choose your interested focused area and tap WhatsApp Chat to start a conversation. Our team will guide you through the joining process, fees, timelines, and the documents needed for enrollment.
Focused Areas
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    Oncology & Cancer Biology

  1. Pan-cancer biomarker discovery using multi-omics integration
  2. Tumor microenvironment deconvolution from bulk RNA-seq
  3. Single-cell atlas of immune states for a chosen cancer
  4. ctDNA minimal residual disease (MRD) detection model design
  5. Neoantigen prediction and immunogenicity ranking pipeline
  6. Copy-number instability scoring and prognosis association study
  7. DNA methylation signatures for early cancer detection
  8. Cancer stemness index modeling and therapy response linkage
  9. Driver pathway analysis for targeted therapy hypotheses
  10. Spatial transcriptomics workflow for tumor–stroma interfaces
  11. Radiogenomics: linking imaging features to molecular subtypes
  12. Liquid biopsy miRNA panel selection with nested cross-validation
  13. Drug synergy prediction for combination therapy design
  14. CRISPR essentiality integration for target prioritization
  15. Mutational signature analysis for etiology inference
  16. HRD scoring and PARP-inhibitor response modeling
  17. Immune checkpoint response predictors with calibration analysis
  18. Organoid assay QC framework for translational screening
  19. Metastasis network modeling and inhibitor shortlisting
  20. Fusion gene discovery and validation plan
  21. Clinical Genomics & Precision Diagnostics

  22. Clinical-grade variant calling and annotation pipeline (research-use)
  23. ACMG-style variant interpretation automation (research-use)
  24. Rare disease phenotype-to-gene prioritization workflow
  25. Copy-number variation (CNV) detection from WES/WGS
  26. Structural variant detection and reporting framework
  27. Trio analysis for de novo variant discovery
  28. Mitochondrial variant analysis and heteroplasmy reporting
  29. Pharmacogenomics panel curation and genotype–phenotype mapping
  30. Hereditary cancer panel design and validation checklist
  31. Somatic tumor-only variant calling and filtering SOP
  32. Microsatellite instability (MSI) scoring workflow
  33. Tumor mutational burden (TMB) pipeline and harmonization checks
  34. HRD score computation and quality controls
  35. Liquid biopsy targeted panel design (amplicon/capture) plan
  36. Variant reclassification monitoring logic (research governance)
  37. De-identified clinical report template + evidence grading rubric
  38. Assay LOD/LOQ planning for ddPCR/qPCR diagnostic prototypes
  39. Contamination and sample-swap detection using SNP fingerprints
  40. Batch effect detection for clinical sequencing runs
  41. Family segregation analysis and penetrance modeling
  42. Single-Cell & Spatial Omics

  43. scRNA-seq QC, doublet removal, and integration benchmark
  44. Cell-type annotation using reference mapping + marker validation
  45. Differential state analysis across conditions with confounder control
  46. Trajectory inference for differentiation or activation programs
  47. Cell–cell communication inference using ligand–receptor methods
  48. scATAC-seq peak calling and gene activity scoring workflow
  49. Multiome (RNA+ATAC) integration and regulatory network inference
  50. Spatial transcriptomics segmentation and spot deconvolution pipeline
  51. Spatially resolved immune infiltration scoring
  52. Cell neighborhood analysis and microenvironment zoning
  53. Batch correction comparison study (Harmony vs Seurat vs Scanpy)
  54. Cell cycle regression impact assessment on clustering outcomes
  55. Rare cell state detection and validation strategy
  56. Reference atlas construction for a chosen tissue
  57. Cross-cohort integration across platforms and protocols
  58. scRNA-seq data imputation benchmarking (with metrics)
  59. Pseudobulk differential expression vs cell-level DE comparison
  60. Gene regulatory network inference from scRNA-seq (SCENIC-style)
  61. Spatial pathway activity mapping and heatmaps
  62. Single-cell signature transfer to bulk cohorts for stratification
  63. Infectious Diseases & Clinical Microbiology

  64. AMR gene detection from WGS with phenotype concordance analysis
  65. Outbreak cluster inference using SNP distances and timelines
  66. Phylogenomic pipeline for hospital surveillance isolates
  67. Metagenomic pathogen detection pipeline (research-use)
  68. Viral genome assembly and lineage assignment workflow
  69. Within-host viral diversity analysis (iSNV tracking)
  70. Transmission chain reconstruction using genomics + metadata
  71. qPCR primer/probe design and in-silico specificity checks
  72. Serology data analysis: neutralization titers and correlates
  73. Host transcriptomic signatures distinguishing viral vs bacterial
  74. Pathogen load modeling across timepoints and outcomes
  75. Sepsis biomarker signature development from public cohorts
  76. Microbial virulence factor profiling and risk scoring
  77. Plasmid reconstruction and AMR mobility analysis
  78. Strain-level metagenomics for gut colonization tracking
  79. Infection-control intervention impact evaluation (before/after)
  80. TB resistance mutation cataloging and decision rules (research)
  81. Fungal pathogen genomics and antifungal resistance mapping
  82. Microbiome–infection susceptibility association study
  83. Clinical isolate QC: contamination, mixed infection detection
  84. Cardio-Metabolic & Endocrine Health

  85. Risk prediction model for diabetes onset using clinical + lab data
  86. Metabolic syndrome clustering and subtype discovery
  87. NAFLD/NASH transcriptomic signature discovery and validation
  88. Atherosclerosis pathway enrichment and key driver analysis
  89. Polygenic risk score construction and calibration (research)
  90. HbA1c trajectory modeling and complication prediction
  91. Hypertension medication response modeling (observational)
  92. Lipidomics signature exploration for CVD outcomes
  93. Obesity microbiome associations with confounder correction
  94. Metformin response biomarker modeling (cohort-based)
  95. Cardiac imaging feature extraction and outcome linkage (research)
  96. Heart failure readmission prediction from EHR time series
  97. Renal function decline modeling in diabetic cohorts
  98. Inflammation markers and cardio-metabolic risk mediation analysis
  99. Glycemic variability metrics and hospitalization outcomes
  100. Thyroid function patterns and cardiovascular endpoints study
  101. PCOS phenotyping using labs + symptoms + ML clustering
  102. Drug safety signal detection for statins using observational data
  103. Diet intervention effects meta-analysis with subgroup modeling
  104. Biomarker panel for early CVD risk (research validation)
  105. Neurology & Psychiatry

  106. Alzheimer’s multi-omics signature integration and staging models
  107. Parkinson’s pathway network analysis and target hypotheses
  108. Epilepsy gene panel curation and evidence mapping
  109. Neuroinflammation transcriptomic signatures across disorders
  110. Depression biomarker modeling using proteomics/transcriptomics
  111. Schizophrenia GWAS-to-gene prioritization workflow
  112. Autism rare variant enrichment and pathway analysis
  113. Brain imaging feature extraction (MRI) and cognition prediction
  114. Sleep pattern modeling from wearable data and symptom links
  115. Stroke outcome prediction using clinical + imaging covariates
  116. CSF biomarker panel validation plan (research-grade)
  117. Neurodegeneration subtype discovery using clustering on omics
  118. Seizure forecasting from EEG feature engineering (research)
  119. Medication adherence prediction using EHR patterns
  120. Suicide risk model evaluation: calibration and fairness checks
  121. Genetic correlation and pleiotropy analysis across traits
  122. Microbiome–gut–brain axis association study (confounder-aware)
  123. Drug repurposing network analysis for neurodegenerative diseases
  124. Longitudinal symptom trajectory modeling for bipolar disorder
  125. Digital phenotyping: smartphone sensor features and mood states
  126. Immunology & Autoimmune Diseases

  127. Autoimmune disease subtype discovery using transcriptomics
  128. Immune repertoire (TCR/BCR) diversity analysis and clonality metrics
  129. Antigen-specific T cell signature modeling from scRNA/TCR
  130. Cytokine panel selection and validation framework (research)
  131. HLA association analysis and fine-mapping workflow
  132. Immune checkpoint gene networks in autoimmunity
  133. Interferon signature quantification and clinical correlation
  134. Cell-state shifts in lupus using single-cell datasets
  135. Rheumatoid arthritis synovial scRNA-seq cell atlas analysis
  136. Multiple sclerosis lesion transcriptomic signature study
  137. Vaccine response predictors from baseline immune profiles
  138. Immune aging (immunosenescence) score development
  139. Allergy sensitization molecular signature discovery
  140. Immune adverse event prediction for immunotherapy (research)
  141. Complement pathway dysregulation modeling in autoimmunity
  142. Autoantibody signature clustering and disease phenotyping
  143. Single-cell ligand–receptor networks in inflamed tissues
  144. Immune cell deconvolution benchmarking across methods
  145. Immunometabolism pathway analysis in chronic inflammation
  146. Immune risk score calibration and external validation
  147. Pharmacology, Drug Discovery & Repurposing

  148. Connectivity mapping for drug repurposing using disease signatures
  149. Network pharmacology target–pathway–drug triad scoring
  150. Virtual screening workflow with docking + consensus scoring
  151. ADMET filtering pipeline and candidate prioritization rubric
  152. Polypharmacology modeling for multi-target drug design
  153. Drug–drug interaction prediction using graph ML (research)
  154. Mechanism-of-action classification from transcriptomic perturbations
  155. Off-target risk mapping using protein networks and alerts
  156. Drug synergy prediction using cell line screening data
  157. PK/PD model template for dose-response interpretation (research)
  158. Target tractability scoring with structural + literature evidence
  159. Clinical trial endpoint ontology mapping for repurposing searches
  160. Real-world evidence cohort emulation for drug effectiveness (research)
  161. Adverse event signal detection from pharmacovigilance datasets
  162. Formulation decision support using physicochemical property models
  163. Drug resistance modeling using longitudinal omics profiles
  164. Protein–ligand interaction feature learning with deep learning (research)
  165. Multi-task ML for predicting bioactivity across targets (research)
  166. Knowledge graph for drug repurposing with evidence weights
  167. Systematic review + meta-analysis automation for drug candidates
  168. Regenerative Medicine & Stem Cells

  169. Stem cell differentiation QC marker panel design
  170. Potency scoring framework for cell therapy batches
  171. Batch effect control for multi-batch differentiation experiments
  172. Single-cell QC of stem-cell derived products (state purity)
  173. Organoid maturation staging and signature development
  174. Scaffold biomaterial selection decision matrix for tissue engineering
  175. iPSC reprogramming efficiency predictors (metadata-driven)
  176. Gene editing QC checklist for cell therapy products (research)
  177. Longitudinal differentiation trajectory modeling (omics-based)
  178. Cell identity authentication pipeline (SNP + expression)
  179. Mycoplasma/contamination risk governance SOP set (research lab)
  180. Release criteria template for non-clinical cell products
  181. Mesenchymal stem cell immunomodulatory signature analysis
  182. Cardiomyocyte differentiation metrics and functional correlations
  183. Neuronal differentiation electrophysiology data analysis plan
  184. 3D bioprinting parameter optimization experiment matrix
  185. Organoid drug screening QC and hit definition SOP
  186. HLA matching strategy primer for allogeneic products (research)
  187. Stability studies design for cell product storage conditions
  188. Reproducibility pack design for regenerative medicine manuscripts
  189. Digital Health, EHR Analytics & Clinical AI

  190. Sepsis early warning model with calibration + drift checks
  191. ICU deterioration prediction using time-series vitals/labs
  192. Readmission risk modeling and subgroup performance audit
  193. Medication error prediction using order patterns (research)
  194. Clinical note NLP for phenotype extraction and validation
  195. Lab result outlier detection and alert triage workflow
  196. Length-of-stay prediction with interpretable models
  197. Bias/fairness audit for a clinical AI model
  198. Model monitoring dashboard design for hospital deployment (research)
  199. Phenotyping via ICD + labs + meds: rules vs ML comparison
  200. Cohort discovery tool using embeddings (privacy-aware)
  201. Adverse drug event detection from notes + structured data
  202. Clinical pathway mining from sequences of care events
  203. Federated learning protocol design for multi-hospital studies
  204. De-identification pipeline evaluation for clinical text
  205. Wearable-derived feature engineering for arrhythmia prediction (research)
  206. Symptom monitoring app analytics and adherence modeling
  207. Clinical trial matching using NLP on eligibility criteria (research)
  208. Explainability study: SHAP vs counterfactuals for EHR models
  209. Outcome definition and label quality audit for EHR studies