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Services and Fees

Next Generation Library Preparation


Library Type Max number of samples that can be multiplexed in one lane WVU Users Non-WVU Users
Each Sample Each Sample
Bead Purification NA $2 $3
Custom Build NA $1 $1
KAPA Hyper DNA Library Prep NA $75 $105
KAPA PCR Reaction NA $2.50 $3.75
Metagenomic Primer Aliquot (50uL at 5uM) NA $2 $3
Illumina compatible gDNA >400 $75 $105
Illumina compatible Stranded mRNA 24 $80 $150
Illumina compatible Small RNA 48 $150 $250
Nextera XT small genome DNA Library Prep
96 $70 $110
Script Seq Epidemiology RNA Library Prep 
24 $225 $315
Script Seq Gold Bacterial RNA Library Prep 
24 $225 $315


MiSeq sequencing

Run Type

Length

WVU User
Non-WVU User
V2 Chemistry


Paired-end 150bp Micro
(2-4 million clusters)
150bp $525 $750
Paired-end 150bp Nano (600k-1million clusters) 150bp $375 $550
Paired-end 250bp Nano 
(600k-1million clusters)
250bp $460 $640
Single-end 50bp 
(~10million clusters)
50bp $830 $1,220
Paired-end 150bp 
(~10million clusters)
150bp $1,300 $1,750
Paired-end 250bp
(~10million clusters)
250bp $1,420 $1,950
V3 Chemistry


Paired-end 75bp
(~20million clusters)
75bp $1,150 $1,650
Paired-end 300bp
(~20million clusters)
300bp $1,850 $2,550


We have a collaborative relationship with the  Marshall University Genomics Core Facility which provides Illumina HiSeq 2500 sequencing for libraries prepared in our facility. Please inquire for pricing. 

Other Sequencing Services



Service Level Single Sample*
(WVU User/Non-WVU User)


Group of 16 Samples** (WVU User/Non-WVU User) Group of 96 Samples** (WVU User/Non-WVU User)
Full Service Sanger Sequencing - includes sequencing reaction†, cleanup, and run on 3130xl $7.50/$12.00 $90/$125 $380/$550
Partial Service Sanger Sequencing - cleanup and reaction performed by user $3.00/$5.00 $25/$32 $90/$115
Fragment Analysis Samples on 3130xl - User performs reaction and provides size standard $3.00/$5.00 $25/$32 $90/$115
RNA Nano (50-500 ng/uL) 6000 Analysis on Agilent 2100 Bioanalyzer‡
(12 sample chip)
$60/$75
RNA Pico (0.5-5 ng/uL) 6000 Analysis on Agilent 2100  Bioanalyzer‡
(12 sample chip)
$60/$75

Bioanalyzer High Sensitivity (0.5-5 ng/uL) DNA Chip‡
(11 sample chip)
$75/$125
Covaris DNA shearing $8/$10
Illumina Library QC via qPCR
(1-12 samples)
$100/$150
Qubit Quantification
Quantify dsDNA or RNA
$3/$5

DNA Size Selection on Blue Pippen $60/$120

* All samples not submitted in multiples of 16 will be charged the single sample price (e.g., if 19 samples are submitted, 16 will be charged at the bulk rate and 3 will be charged at the single sample rate). Such samples may experience a processing delay.
** We ask that you leave one well available for the inclusion of a positive control.
† Assumes M13 or other standard primers. Custom primers should be provided by individual researchers. Submission conditions vary depending on sample type. Please contact the lab manager for details.
‡ Please provide at least one week advance notice for use of the BioAnalyzer to allow time for ordering, if necessary.

Available Primers


Primer Name Sequence
SP6_Promoter TACGATTTAGGTGACACTATAG
BGH_Reverse TAGAAGGCACAGTCGAGG
CMV_Forward CGCAAATGGGCGGTAGGCGTG
T3_Promoter AATTAACCCTCACTAAAGGG
T7_Promoter TAATACGACTCACTATAGGG
M13_Forward (-20)   GTAAAACGACGGCCAGT
M13_Reverse (-27) CAGGAAACAGCTATGAC
Luc_F AGTCAAGTAACAACCGCGA
LKO.15-Human U6 promoter GACTATCATATGCTTACCGT
SV40pA-R GAAATTTGTGATGCTATTGC
TRIPZ/GIPZ_HairpinSeq GTTTGTTTGAATGAGGCTTC
pGEX_F GGGCTGGCAAGCCACGTTTGGTG
pGEX_R CCGGGAGCTGCATGTGTCAGAGG
CMV_Prom_F TAGGCGTGTACGGTGGGAG



Bioinformatics


All bioinformatics services are charged at an hourly rate of $30/hr for WVU users and $35/hr for external users. This time includes just the time a bioinformatician is actively engaged with your data. There is currently no charge for computational time. Below is a list of common tasks and an estimate for how long they will take. Note that this is by no means a comprehensive list of available services; it's just a few easily quantifiable tasks. A few things we can also help with include:

  • Experiment design
  • Grant writing
  • Large data sets
  • Mining public databases
  • Automation of repetitive tasks
  • Publication quality figures
  • Interactive visualizations
  • Custom analyses
  • Training


Service Estimate
(hours)
RNA-seq
With reference genome in Ensembl, one comparison, identified samples, less than 16 samples 6
Extra Comparisons + 1
Without a reference 20-40
Metagenomics
16S Metagenomics: classify strains, PCoA, rarefaction, diversity 5
Fungal ITS: classify strains, PCoA, rarefaction, diversity 5
Identify significantly different species + 2
All prices subject to change 

Last updated March 2018.