Skip to Content

Pricing and Forms

Please be aware that the fees listed below are applicable only to investigators from MD Anderson, Baylor College of Medicine and other institutions with whom MD Anderson has a formal affiliation. Other external academic institutions or industry colleagues requesting services from the ncRNA Program are subject to a different pricing structure. All work is provided on a fee-for-service basis and is first come, first served.

Bioanalyzer and Nanodrop

  • Nanodrop™: $1 (per sample)
  • RNA 6000 Nano/Pico Assay  (1 to 12 samples): $35
  • Protein Assay  (1 to 10 samples): $35
  • DNA Assay  (1 to 12 samples): $35

miRNA/ncRNA Expression Profiling (Package)

  • 15K Human and Mouse miRNA/ncRNA/UCR Profiling: $350

SOLiD™ Next Generation Sequencing*

  • Please request quote*

Affymetrix GeneChip® - Sample Processing

  • GeneChip analysis from total RNA (transcription profiling): $350
  • GeneChip analysis from total RNA (exon profiling): $400
  • GeneChip analysis from cDNA (transcription profiling): $200
  • GeneChip analysis from cRNA (transcription profiling): $120
  • SNP Analysis from Genomic DNA (SNP 6.0 Genotyping): $400

Affymetrix GeneChip® - Chip Only

  • Human Genome U133 plus 2.0: $425
  • Mouse Genome 430 2.0: $425
  • Rat Genome 230 2.0: $400
  • Human Mapping SNP 6.0: $300
  • Other Chip type: Please request quote

Real-Time qRT-PCR

  • Real-Time qRT-PCR on ABI 7900HT (96 or 384 format): $40 (per run)

Expression Analysis

  • Visual Analysis of High-Dimensional Data/Partek Pro: No Charge
  • Data Change Calculation: No Charge
  • Pairwise Comparison: No Charge
  • Advanced Analysis of Microarray and Sequence Data: $70 (per hour)

*The service fee for SOLiD next generation sequencing is based on the number of sequences run and the number of sample libraries to be prepared in a multiplexing run. Each protocol (fragment library, mate-paired library and pair end library) for library preparation has a different fee. The number of samples to be multiplexed in a run depends on the complexity of the samples (genomic DNA-seq, whole transcriptome-seq, small RNA-seq, CHIP-seq, etc.) provided and data coverage per sample requested (5x, 10x, 15x or 20x).

The Sequencing and Non-Coding RNA Program will perform a project assessment for SOLiD next generation sequencing requests to determine a cost and time estimate based on the volume of proposed samples submitted by the investigator. For more information, please contact either Dr. Chang-gong Liu or Dr. Xiuping Liu at 713-745-8182.


© 2014 The University of Texas MD Anderson Cancer Center