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Library Preparation only
CGC Service Center Internal1 Academic2 mRNA-seq $114/sample $149/sample Total RNA-seq $162/sample $209/sample sRNA-seq (small RNA-seq) for micro RNA $144/sample $179/sample ChIP-seq $144/sample $189/sample ATAC-seq $199/sample $249/sample Ultra-low Input mRNA-seq $164/sample $209/sample Ultra-low input total RNA-seq $179/sample $249/sample Ultra-low input small RNA-seq $194/sample $249/sample scRNA-seq (1st sample) $2499/sample $3299/sample scRNA-seq (2nd-8th samples) $1999/sample $2499/sample scRNA-seq+CRISPR (1st sample) $2639/sample $3299/sample scRNA-seq+CRISPR (2nd-8th samples) $2139/sample $2699/sample Multiome (snATAC-seq +snRNA-seq) (1st sample) $3899/sample $4899/sample Multiome (snATAC-seq +snRNA-seq) (2nd 8th sample) $3499/sample $4399/sample 5’ scRNA-seq (GEX only, 1st sample) $2799/sample $3399/sample 5’ scRNA-seq (GEX only, 2nd-8th samples) $2099/sample $2599/sample 5’ scRNA-seq (GEX +TCR or BCR, 1st sample) $2899/sample $3599/sample 5’ scRNA-seq (GEX +TCR or BCR, 2nd-8th samples) $2199/sample $2799/sample 5’ scRNA-seq (GEX +TCR +BCR, 1st sample) $2999/sample $3699/sample 5’ scRNA-seq (GEX +TCR +BCR, 2nd-8th samples) $2319/sample $2899/sample Flex scRNA-seq (4 samples, 10000 cells/sample) $4899/reaction $6099/reaction Visium CytAssist (spatial transcriptomics, 6.5mm) $2199/sample $2799/sample Visium CytAssist (spatial transcriptomics, 11mm) $4299/sample $5399/sample Visium CytAssist HD (spatial transcriptomics, 6.5mm) $3699/section $4699/section Parse scRNAseq inquiry inquiry -
Xenium Assay (user provides 10x Genomics kits)
Internal1 Academic2 Samples handling fees (2 slides for 1 run) $500/run $600/run Xenium Analyzer Operation fee $350/day $420/day -
Library and Sequencing **
Internal1 Academic2 WES (human 100x) $349/sample $379/sample WGS (30x) $600/sample $720/sample mRNA-seq (>= 20 samples) $159/sample $209/sample mRNA-seq (< 20 samples) $179/sample $239/sample sRNA-seq (>= 20 samples, 10M reads, 75SE) $189/sample $249/sample sRNA-seq (< 20 samples, 10M reads, 75SE) $209/sample $279/sample ChIP-seq (>= 20 samples) $189/sample $249/sample ChIP-seq (<20 samples) $209/sample $279/sample Total RNA-seq (>= 20 samples, 30M reads, 150PE) $229/sample $299/sample Total RNA-seq (<20 samples, 30M reads, 150PE) $259/sample $329/sample Ultra-low Input mRNA-seq (>=20 samples) $209/sample $269/sample Ultra-low Input mRNA-seq (<20 samples) $239/sample $299/sample Ultra-low Input total RNA-seq (40M, 150PE) $269/sample $339/sample Ultra-low Input small RNA-seq(>=20 samples, 10M reads, 75SE) $239/sample $249/sample Ultra-low Input small RNA-seq(<20 samples, 10M reads, 75SE) $269/sample $349/sample ATAC-seq (60M, 150PE) $339/sample $424/sample -
Sequencing
Internal1 Academic2 NextSeq 400M reads 75SE***/36PE $2499 $3199 NextSeq 400M reads 75PE**** $4499 $5699 NextSeq 130M reads 75PE $1999 $2499 Novaseq 1000M reads 150PE $2100 $2600 -
Other *****
Internal1 Academic2 RNA RIN assay $50/11 samples $60/11 samples DNA bioanalyzer assay $100/11 samples $125/11 samples -
Bioinformatics Service (hourly rate)
Internal1 Academic2 Standard Analysis for bulk RNAseq Fastq QC $5/sample $8/sample Fastq Trimming $5/sample $8/sample Alignment, gene counts & Normalization
(human or mouse only)$25/sample $30/sample NGS customized analysis (currently unavailable) $150/hour $180/hour Sequencing consultation No charge No charge Bioinformatics consultation No charge No charge
The prices listed are under adjustment by the core at any time, and the core has the right to interpret these prices.
- Internal: The price provided to all the faculties in UTHealth at Houston and the faculties in academic institutes within Texas with a cancer project after registering as a CGC user.
- Academic: The price provided to all academic institutes inside United States.
- * The prices of scRNA-seq depend on the targeted cell number and the sequencing depth.
- ** If not indicated, the sequencing depth is 20M paired reads of 150PE.
- *** SE: single-end sequencing.
- **** PE: paired-end sequencing.
- ***** If library preparation or/and sequencing services are not included in the project, a handling fee may apply for these services.
Please don't hesitate to contact us for more information if the targeted cell number and the sequencing depth differ from the list.