30 structures-"https:"-"https:"-"https:"-"https:"-"https:" positions at Baylor College of Medicine
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Job Description Apply now Job Title: Medical Director, Structural Heart Disease (Associate Professor or Professor) Division: Medicine Work Arrangement: Location: Houston, TX Salary Range: FLSA
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homeostasis. Responsibilities include recombinant protein expression and purification, development and execution of enzyme and biophysical assays, and quantitative data analysis to support structure–function
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PacBio HiFi, Oxford Nanopore, and graph-based genome technologies. Job Duties Develops, implements, and optimizes algorithms and computational methods for structural variant (SV), tandem repeat (TR), and
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collaboration and coordination within a complex organizational and implementation structure. Gains an understanding of global health programs and interventions in a variety of countries. Gains exposure to global
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retrievability. Uploads digital files to our internal shared drive system, ensuring proper folder structure and permissions. Coordinates with lab staff to identify and appropriately handle sensitive
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commitment to fostering a collaborative lab environment and promoting positive group dynamics. Minimum Qualifications Ph.D. in Chemistry, Computational Sciences, Computational Biology, Structural Biology
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genetics. Genomic analyses: next generation sequencing - DNA and transcriptome, chromosomal microarrays, cell culture, qPCR, gene regulation assays, 3D chromatin structure. Prior experience in the area of
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field. No experience required. Preferred Qualifications Ph.D. in Chemistry, Computational Sciences, Computational Biology, Structural Biology, Computer Science, Bioinformatics, Statistics, or related
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specialized construction jobs as needed such as HVAC, plumbing, and architectural construction. Performs energy management system configuration and maintenance. Performs other job-related duties as assigned
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for structural variant (SV), tandem repeat (TR), and methylation analysis in long-read sequencing data. Lead population-scale analyses involving thousands of long-read genomes, including data QC, variant calling