UNMC_Acronym_Vert_sm_4c
University of Nebraska Medical Center

Pricing

The Bioinformatics and System Biology Core offers the initial consultation for free. The services required will be discussed during the initial consultation phase. The time required for the service will be estimated during the first consultation. For each project, a cost center number should be provided before we initiate the work.

Hourly Charges (Non-Sample Based)

Services provided by Rate
Analyst $60/hour
System Administrator $70/hour
Director $80/hour

Sample-Based Services and Charges:

Type of service Rate
RNA sequencing Up to 12 samples: $100 per sample
Additional samples: $75 per sample (see note 4 below)
Exome sequencing Up to 12 samples: $100 per sample
Additional samples: $75 per sample
Whole-genome sequencing Up to 12 samples: $150 per sample
Additional samples: $125 per sample
RNA sequencing / DNA sequencing for specific gene panel Up to 50 samples: $50 per sample
51-100 samples: $40 per sample
Additional samples: $30 per sample
10x Genomics single cell First library: $250 (within one run)
Additional libraries: $100 per library (within one run)
Aggregation for multiple libraries: $50 per library
Metagenomics – Whole-genome sequencing Up to 12 samples: $100 per sample
Additional samples: $75 per sample
Metagenomics – 16s $50 per sample
Microbial de novo assembly $50 per sample
Ingenuity Pathways Analysis $100 per comparison
Gene Set Enrichment Analysis $100 per comparison
NIH Gene Expression Omnibus submission (RNA sequencing or microarray data) Up to 12 samples: $100 per submission
Additional samples: additional hourly basis / submission
NIH Sequence Read Archive submission (DNA sequencing exome or whole-genome data) Hourly basis

Notes:

  1. The rates mentioned above are a subsidized rate for the services provided to UNMC investigators.
  2. The rates for other academic institutions and corporations are 1.5X and 2X the mentioned rate respectively.
  3. For RNA-seq and metagenomics statistical comparisons, the N (sample size)/three comparisons are included in the sample-size based quote. More comparisons will be charged by 0.5 hour per comparison.
  4. Additional samples should be a part of the same batch and aligned to the same reference genome. If the batch has more than 12 samples, but needs to be aligned to the different reference genomes, it is charged at a regular rate.