San Diego, CA · On-site
$52.95 - $72.81/hr
Experience analyzing next-gen sequencing data from raw sequencing output (BCL/FASTQ) through alignment, variant calling, annotation, and prioritization for whole genome or exome sequencing data.
San Diego, CA · On-site
$52.95 - $72.81/hr
Experience analyzing next-gen sequencing data from raw sequencing output (BCL/FASTQ) through alignment, variant calling, annotation, and prioritization for whole genome or exome sequencing data.
The successful candidate will lead computational and statistical analyses of large-scale genomic datasets, including whole-genome, whole-exome, and transcriptomic sequencing, to advance projects in ...
The successful candidate will lead computational and statistical analyses of large-scale genomic datasets, including whole-genome, whole-exome, and transcriptomic sequencing, to advance projects in ...
... whole exome sequencing and RNA-seq-analysis of clonal evolution of cancer, dot blots, RNA modification-seq, ChIP-seq, RIP-seq, PAR-CLIP-seq, single-cell sequencing, spatial sequencing, metabolism ...
... whole exome sequencing and RNA-seq-analysis of clonal evolution of cancer, dot blots, RNA modification-seq, ChIP-seq, RIP-seq, PAR-CLIP-seq, single-cell sequencing, spatial sequencing, metabolism ...
... whole exome sequencing and RNA-seq-analysis of clonal evolution of cancer, dot blots, RNA modification-seq, ChIP-seq, RIP-seq, PAR-CLIP-seq, single-cell sequencing, spatial sequencing, metabolism ...
... whole exome sequencing and RNA-seq-analysis of clonal evolution of cancer, dot blots, RNA modification-seq, ChIP-seq, RIP-seq, PAR-CLIP-seq, single-cell sequencing, spatial sequencing, metabolism ...
... whole exome sequencing and RNA-seq-analysis of clonal evolution of cancer, dot blots, RNA modification-seq, ChIP-seq, RIP-seq, PAR-CLIP-seq, single-cell sequencing, spatial sequencing, metabolism ...
... whole exome sequencing and RNA-seq-analysis of clonal evolution of cancer, dot blots, RNA modification-seq, ChIP-seq, RIP-seq, PAR-CLIP-seq, single-cell sequencing, spatial sequencing, metabolism ...
San Diego, CA · On-site
$52.95 - $72.81/hr
Experience analyzing next-gen sequencing data from raw sequencing output (BCL/FASTQ) through alignment, variant calling, annotation, and prioritization for whole genome or exome sequencing data.
San Diego, CA · On-site
$52.95 - $72.81/hr
Experience analyzing next-gen sequencing data from raw sequencing output (BCL/FASTQ) through alignment, variant calling, annotation, and prioritization for whole genome or exome sequencing data.
... whole exome sequencing and RNA-seq-analysis of clonal evolution of cancer, dot blots, RNA modification-seq, ChIP-seq, RIP-seq, PAR-CLIP-seq, single-cell sequencing, spatial sequencing, metabolism ...
... whole exome sequencing and RNA-seq-analysis of clonal evolution of cancer, dot blots, RNA modification-seq, ChIP-seq, RIP-seq, PAR-CLIP-seq, single-cell sequencing, spatial sequencing, metabolism ...
... whole exome sequencing and RNA-seq-analysis of clonal evolution of cancer, dot blots, RNA modification-seq, ChIP-seq, RIP-seq, PAR-CLIP-seq, single-cell sequencing, spatial sequencing, metabolism ...
... whole exome sequencing and RNA-seq-analysis of clonal evolution of cancer, dot blots, RNA modification-seq, ChIP-seq, RIP-seq, PAR-CLIP-seq, single-cell sequencing, spatial sequencing, metabolism ...
Whole exome sequencing (WES) * Whole genome sequencing (WGS) * RNA sequencing * Single-cell ... Evaluate and implement cloud-based analytics platforms and scalable computational infrastructure.
Whole exome sequencing (WES) * Whole genome sequencing (WGS) * RNA sequencing * Single-cell ... Evaluate and implement cloud-based analytics platforms and scalable computational infrastructure.
... exome sequencing (WES), and emerging long-read sequencing technologies. In addition to data analysis, BiNGS develops bioinformatics tools, manages computational infrastructure, provides access to ...
... exome sequencing (WES), and emerging long-read sequencing technologies. In addition to data analysis, BiNGS develops bioinformatics tools, manages computational infrastructure, provides access to ...
Hagerstown, MD · On-site
$350K - $400K/yr
Whole genome or exome sequencing and polygenic risk scoring across cardiovascular, oncologic ... Microbiome analysis, nutrient profiling, heavy metal testing * Frailty index, cognitive function ...
Hagerstown, MD · On-site
$350K - $400K/yr
Whole genome or exome sequencing and polygenic risk scoring across cardiovascular, oncologic ... Microbiome analysis, nutrient profiling, heavy metal testing * Frailty index, cognitive function ...
... exome sequencing (WES), and emerging long-read sequencing technologies. In addition to data analysis, BiNGS develops bioinformatics tools, manages computational infrastructure, provides access to ...
... exome sequencing (WES), and emerging long-read sequencing technologies. In addition to data analysis, BiNGS develops bioinformatics tools, manages computational infrastructure, provides access to ...
Phoenix, AZ · On-site
This position provides high-level scientific expertise in the analysis of genetic testing data, including next-generation sequencing (NGS) panels, whole exome sequencing (WES), and whole genome ...
Phoenix, AZ · On-site
This position provides high-level scientific expertise in the analysis of genetic testing data, including next-generation sequencing (NGS) panels, whole exome sequencing (WES), and whole genome ...
Hagerstown, MD · On-site
$350K - $400K/yr
Whole genome or exome sequencing and polygenic risk scoring across cardiovascular, oncologic ... Microbiome analysis, nutrient profiling, heavy metal testing * Frailty index, cognitive function ...
Hagerstown, MD · On-site
$350K - $400K/yr
Whole genome or exome sequencing and polygenic risk scoring across cardiovascular, oncologic ... Microbiome analysis, nutrient profiling, heavy metal testing * Frailty index, cognitive function ...
Phoenix, AZ · On-site
This position provides high-level scientific expertise in the analysis of genetic testing data including next-generation sequencing (NGS) such including NGS panels, whole exome sequencing (WES), and ...
Phoenix, AZ · On-site
This position provides high-level scientific expertise in the analysis of genetic testing data including next-generation sequencing (NGS) such including NGS panels, whole exome sequencing (WES), and ...
Lead analyses supporting biomarker discovery, patient selection, pharmacodynamic assessments, and ... Whole exome sequencing (WES) * Whole genome sequencing (WGS) * RNA sequencing * Single-cell ...
Lead analyses supporting biomarker discovery, patient selection, pharmacodynamic assessments, and ... Whole exome sequencing (WES) * Whole genome sequencing (WGS) * RNA sequencing * Single-cell ...
Experience with exome and/or genome sequencing, analysis and interpretation of genetic variants, and functional characterization of disease-associated variants is also preferred. Applicants must have ...
Experience with exome and/or genome sequencing, analysis and interpretation of genetic variants, and functional characterization of disease-associated variants is also preferred. Applicants must have ...
San Carlos, CA · On-site
... HT/HTLs in analyzing specimens and maintaining equipment in good condition. PRIMARY ... exome sequencing laboratory with little to no errors Duties may include but not limited to ...
San Carlos, CA · On-site
... HT/HTLs in analyzing specimens and maintaining equipment in good condition. PRIMARY ... exome sequencing laboratory with little to no errors Duties may include but not limited to ...
Develop and apply computational, statistical, and AI/ML approaches to analyze diverse biological datasets, including: * GWAS, whole-genome/exome sequencing * DNA methylation and epigenomic profiling
Develop and apply computational, statistical, and AI/ML approaches to analyze diverse biological datasets, including: * GWAS, whole-genome/exome sequencing * DNA methylation and epigenomic profiling
Whole genome or exome sequencing and polygenic risk scoring across cardiovascular, oncologic ... Microbiome analysis, nutrient profiling, heavy metal testing * Frailty index, cognitive function ...
Whole genome or exome sequencing and polygenic risk scoring across cardiovascular, oncologic ... Microbiome analysis, nutrient profiling, heavy metal testing * Frailty index, cognitive function ...
$35K - $43.7K
2% of jobs
$43.7K - $52.5K
17% of jobs
$54.7K is the 25th percentile. Wages below this are outliers.
$52.5K - $61.2K
23% of jobs
The median wage is $65.9K / yr.
$61.2K - $69.9K
15% of jobs
$69.9K - $78.6K
13% of jobs
$83.7K is the 75th percentile. Wages above this are outliers.
$78.6K - $87.4K
9% of jobs
$87.4K - $96.1K
7% of jobs
$96.1K - $104.8K
4% of jobs
$104.8K - $113.5K
3% of jobs
$113.5K - $122.3K
4% of jobs
$122.3K - $131K
2% of jobs
$35K
$75.5K
$131K
| Aspect | Exome Sequencing Analyst | Genetic Data Analyst |
|---|---|---|
| Required Credentials | Bachelor's or Master's in Genetics, Molecular Biology, or related field; experience with sequencing technologies | Bachelor's or Master's in Bioinformatics, Genetics, or related; strong data analysis skills |
| Work Environment | Laboratories, research institutions, biotech companies | Healthcare, research, biotech firms, data-focused environments |
| Industry Usage | Genomics, personalized medicine, research labs | Healthcare analytics, research, biotech industry |
While both roles involve genetic data analysis, Exome Sequencing Analysts focus specifically on sequencing data from exomes, interpreting genetic variants, and working closely with laboratory technologies. Genetic Data Analysts may work with broader genetic datasets, including genome-wide data, and often emphasize data management and statistical analysis. Both roles require strong bioinformatics skills but differ in their specific focus and work environment.
For Exome Sequencing Analyst jobs, the most frequently searched job titles are:
San Diego, CA • On-site
$52.95 - $72.81/hr
Full-time
Re-posted yesterday
8.1
Based on 47 frontline employees who took The Breakroom Quiz
119th of 1,066 rated hospitals
Hybrid role.
JOB SUMMARY:
Join a pioneering team of clinicians, bioinformaticians, and software engineers defining the future of rapid clinical genomics. As a Senior Bioinformaticist, you will serve as a core computational lead responsible for scaling, hardening, and evolving our high-throughput, ultra-rapid whole genome sequencing (WGS) framework.
This role sits at the intersection of production-grade engineering, clinical practice, and cutting-edge discovery. You will work side-by-side with hospital clinicians to analyze patient genomic data directly, transforming complex computational findings into real-time clinical decisions that directly impact patient outcomes. Beyond maintaining fast, reliable production pipelines, you will drive our expanding technical roadmap: deeply integrating AI/ML workflows across genomic domains, tackling complex structural variant analysis, and building out multi-omics computational frameworks.
If you are eager to build production biocomputing systems while leveraging next-generation algorithms, and want your daily work to directly change patient lives, this position offers an extraordinary platform for growth, industry collaboration, and real-world impact.
MINMUM QUALIFICATIONS:
Master's Degree
Area of study in a field related to the position.
Experience analyzing next-gen sequencing data from raw sequencing output (BCL/FASTQ) through alignment, variant calling, annotation, and prioritization for whole genome or exome sequencing data.
Experience developing, maintaining, and troubleshooting automated bioinformatics pipelines supporting high-throughput genomic analysis in production or research environments.
Experience working with and understanding of NGS analysis tools like Dragen, BWA,, GATK, DeepVariant, Samtools, bcftools, Picard, Annovar, VEP, or similar tools.
Experience with Unix/Linux operating system and software development using any of Ruby, Python, Perl, Bash.
Experience working with large-scale computational environments, including HPC or distributed compute systems, and workflow orchestration tools (e.g., Nextflow, Snakemake, WDL, Cromwell, or similar frameworks).
PREFERRED QUALIFICATIONS:
Ph.D.
Experience in CNV and SV detection tools and interpretation of complex genomic variation.
Previous experience working in a CAP/CLIA environment.
Previous experience with cloud-based development or analysis and performing benchmarking of bioinformatics tools.
Experience applying machine learning or AI approaches to genomics, phenomics, or biomedical datasets.
Experience analyzing multi-omics datasets, including RNA-seq, long-read sequencing, transcriptomics, proteomics, or related genomic technologies.
The current salary range for this position is $52.95 to $72.81
Rady Children’s Hospital is committed to compensation that is externally competitive and internally equitable. We demonstrate this commitment by conducting regular market reviews to remain competitive with organizations of similar size in the nonprofit, healthcare sector. The range listed above does not represent the full salary range for the position but is the expected hiring range for qualified candidates. Compensation decisions consider a variety of factors including experience, education, licensure, unique skillsets, organizational need, and internal equity. This posting will remain open from the “date posted” until the hiring manager has determined there is a sufficient applicant pool or until the position is filled.
Get the full story on Breakroom
Sourced by ZipRecruiter
Hospitals
5,001 - 10,000 Employees
San Diego, CA, US
1954
