Senior Bioinformatics Scientist

Net2Source (N2S); Cambridge (MA); On-site; USD 140,000 - 200,000; Full time

Job summary

Net2Source (N2S) invites applications for a Senior Bioinformatics Scientist III in Cambridge, MA. This 2-year contract role focuses on integrating human genetic data with multi-omics, applying ML to biomarker discovery and patient stratification, and supporting target identification.

The candidate will lead data ingestion, QC, imputation, GWAS/QTL analyses, and multi-omics integration using HPC and AWS, with emphasis on reproducibility and collaboration.

Qualifications

• Ph.D. in Genetics, Genomics, Statistical Genetics, Computational Biology, or a related field.
• A proven track record of over 5 years in genetic data analysis.
• Strong understanding of statistical methods and genetic data analysis and integration.
• Experience applying machine learning to high-dimensional biological data.
• Hands-on experience integrating multi-omics data with genetic data.
• Proficiency in R, Python, and Bash; reproducible analyses.
• Experience with HPC and AWS Cloud Computing.

Responsibilities

• Data Ingestion: query and harmonize external resources for genetic and multi-omics datasets.
• Genetic/Genomic Data Analysis: QC, imputation, variant calling and annotation.
• Statistical Genetics: GWAS/PheWAS, fine-mapping, colocalization, polygenic scores.
• QTL Analysis: eQTL, sQTL, pQTL mapping with tensorQTL/PLINK/R/qtl.
• Population Genetics Analysis: allele frequencies, LD, ancestry structure.
• Machine Learning: build/benchmark models for variant effect prediction and patient stratification.
• Multi-Omics Data Integration: integrate transcriptomics, proteomics, epigenomics with genetics.
• Documentation: reproducible workflows using Git, Nextflow, Snakemake.

Skills

R

Python

Bash

HPC

AWS

ML for genomics

Multi-omics integration

Statistical genetics

GWAS / QTL

Education

Ph.D. in Genetics

Tools

GATK

bcftools

samtools

ANNOVAR

VEP

PLINK

REGENIE

Job description

Job Title: Senior Bioinformatics Scientist III

Location: Cambridge, MA 02141

100% onsite

Duration: 2 Years Contract

Shift: Monday Thru Friday (8 AM to 5 PM) - 40 Hours/Week

Position Summary:

The Precision Genetics group within the Data and Genome Sciences Department is seeking a skilled Contractor to join our Computational Precision Genetics team. We are looking for a data scientist who combines deep expertise in human genetic data analysis with strong machine learning capabilities and hands-on experience integrating multi-omics data, to support our target identification, patient stratification, and biomarker discovery efforts.

Key Responsibilities:

• Data Ingestion: Query and harmonize external resources to acquire relevant genetic, genomic, and multi-omics datasets (e.g., dbSNP, 1000 Genomes Project, gnomAD, GTEx, Ensembl, Open Targets, ClinVar, GWAS Catalog, UK Biobank, Gene Expression Omnibus).
• Genetic/Genomic Data Analysis: Perform quality control (QC) and analysis of genetic/genomic data, including genotype imputation from array data, variant calling and annotation using state-of-the-art methods (e.g., IMPUTE, Minimac, Eagle, BEAGLE, GATK, bcftools, samtools, ANNOVAR, VEP).
• Statistical Genetics: Conduct genetic association analyses at scale, including GWAS/PheWAS, rare-variant burden and collapsing tests, fine-mapping, colocalization, polygenic scores, and Mendelian randomization (e.g., PLINK, REGENIE, SAIGE, GCTA, SuSiE, coloc, LDSC).
• QTL Analysis: Conduct QTL analysis to identify genetic loci associated with quantitative and molecular traits, including eQTL, sQTL, and pQTL mapping, utilizing tools such as tensorQTL, FastQTL, PLINK, or R/qtl.
• Population Genetics Analysis: Analyze genetic variation across populations, including allele frequency estimation, linkage disequilibrium, relatedness, and ancestry/population structure analysis.
• Machine Learning: Develop, benchmark, and validate machine learning models on high-dimensional genetic and molecular data for tasks such as variant effect prediction, patient stratification, and biomarker or treatment-response prediction; apply rigorous cross-validation, control for batch and ancestry confounding, and use interpretability methods to translate models into testable biological hypotheses (e.g., scikit-learn, XGBoost, PyTorch, SHAP).
• Multi-Omics Data Integration: Integrate genetic datasets with other omics layers, including transcriptomic (bulk and single-cell RNA-seq), epigenomic, proteomic (e.g., OLINK, mass spectrometry), and spatial data, to provide comprehensive insights into gene function and disease biology (e.g., DESeq2, limma, Seurat, scanpy).
• Documentation and Reproducibility: Prepare detailed documentation of analysis methods and results in a timely manner, and deliver version-controlled, reproducible analysis workflows (e.g., Git, Nextflow, Snakemake).

Required Qualifications:

• Ph.D. in Genetics, Genomics, Statistical Genetics, Computational Biology, or a related field.
• A proven track record of over 5 years in genetic data analysis.
• Strong understanding of statistical methods and genetic data analysis and integration (e.g., variant analysis, GWAS and QTL mapping, population genetics, genomic annotations).
• Demonstrated experience applying machine learning to high-dimensional biological data, including feature engineering, model selection, validation, and avoidance of overfitting and confounding.
• Hands-on experience integrating multi-omics data (e.g., transcriptomics, proteomics, epigenomics) with genetic data.
• Proficiency in R, Python, and Bash, with the ability to establish best practices for reproducible data analyses.
• Experience with high-performance computing (HPC) systems and AWS Cloud Computing (e.g., IAM, S3 buckets).
• A collaborative and self-motivated individual with a strong work ethic, capable of managing multiple objectives in a dynamic environment and adapting to changing priorities.
• Excellent written and verbal communication skills.

Preferred Qualifications:

• Experience with real-world and large-scale biobank genetic data (e.g., UK Biobank, All of Us, FinnGen, electronic health record-linked cohorts).
• Experience with deep learning approaches for genomics, including sequence-based and variant-effect prediction models.
• Familiarity with single-cell and spatial transcriptomics analysis.
• Experience supporting drug target identification and validation, or biomarker discovery in a pharmaceutical or biotechnology setting.
• Familiarity with workflow managers (e.g., Nextflow, Snakemake) and containerization (e.g., Docker, Singularity).
• Proficient in human genetic/human genomic data analysis tools and techniques-e.g., variant analysis, population genetics, genomic annotations.
• Multi-Omics Data Integration
• Proficiency in R, Python, and Bash.
• High-performance computing (HPC) systems and AWS Cloud Computing (e.g., IAM, S3 buckets).