Genetic Resources Core Facility DNA Services

For 8 channel or less pipettes.

For pipettes with 9 or more channels.

Full service includes:

• Pretesting with the ability to replace/drop poor performing samples
• 2 controls per plate
• Study duplicates at no additional cost
• Individual sample reruns in the lab for poor performance (repeated 1X)
• Full data release, which includes hapmap concordance, reproducibility of genotype calculations broken down by MAF bin for each sample pair, GenomeStudio project, SNP and samples tables, full SNP technical filter applied, samples reclustered on own data, final reports, PLINK file and README docs explaining the data in each directory

This service level includes:

• Pretesting with the ability to replace/drop poor performing samples
• Study duplicates at no additional cost
• Full data release, which includes hapmap concordance, reproducibility of genotype calculations broken down by MAF bin for each sample pair, GenomeStudio project, SNP and samples tables, full SNP technical filter applied, samples reclustered on own data, final reports, PLINK file and README docs explaining the data in each directory

We will not supply any controls nor will we redo any samples that fail.  Each sample will be run once in the lab.

This service level includes:

• Study duplicates at no additional cost
• 2 controls per plate
• Individual sample reruns in the lab for poor performance (repeated 1X)
• Full data release, which includes hapmap concordance, reproducibility of genotype calculations broken down by MAF bin for each sample pair, GenomeStudio project, SNP and samples tables, full SNP technical filter applied, samples reclustered on own data, final reports, PLINK file and README docs explaining the data in each directory

Samples will be run as submitted, with no pretesting.

This service level includes:

• Study duplicates at no additional cost
• 2 Controls per plate
• Individual sample reruns in the lab for poor performance (repeated 1X)
• idtats, a GenomeStudio project and a PLINK file.  

We will not run a technical filter on your data, so you will need to clean and remove all failed assays from the provided data set.  To visualize and clean the data you will need access to a copy of GenomeStudio from Illumina or similar software from a 3rd party vendor that uses .idat files as input.  Our data release will include the standard .egt file from Illumina, but it will not have been optimized for your specific data.  

You should expect an FTE data analyst to spend at least two weeks cleaning the data after you receive it from us.

This service level includes:

• Study duplicates at no additional cost
• 2 Controls per plate
• Individual sample reruns in the lab for poor performance (repeated 1X)
• idtats, a GenomeStudio project and a PLINK file.  

We will not run a technical filter on your data, so you will need to clean and remove all failed assays from the provided data set.  To visualize and clean the data you will need access to a copy of GenomeStudio from Illumina or similar software from a 3rd party vendor that uses .idat files as input.  Our data release will include the standard .egt file from Illumina, but it will not have been optimized for your specific data.  

You should expect an FTE data analyst to spend at least two weeks cleaning the data after you receive it from us.

Covaris truXTRAC Covaris truXTRAC or Qiagen 

Full service includes:

• Pretesting with the ability to replace/drop poor performing samples
• 2 Controls per plate
• Study duplicates at no additional cost
• Individual sample reruns in the lab for poor performance (repeated 1X)
• Full data release which includes hapmap concordance, reproducibility of genotype calculations broken down by MAF bin for each sample pair, GenomeStudio project, SNP and samples tables, full SNP technical filter applied, samples reclustered on own data, final reports, PLINK file and README docs explaining the data in each directory

(~200mm2 for a 5µm section), Covaris truXTRAC or Qiagen 

(~200mm2 for a 5µm section), Covaris truXTRAC or Qiagen 

This service level includes:

• 2 controls per plate
• Study duplicates at no additional cost
• Individual sample reruns in the lab for poor performance (repeated 1X)
• Full data release, which includes hapmap concordance, reproducibility of genotype calculations broken down by MAF bin for each sample pair, GenomeStudio project, SNP and samples tables, full SNP technical filter applied, samples reclustered on own data, final reports, PLINK file and README docs explaining the data in each directory

This service level includes:

• 2 controls per plate
• Study duplicates at no additional cost
• Individual sample reruns in the lab for poor performance (repeated 1X)
• Full data release, which includes hapmap concordance, reproducibility of genotype calculations broken down by MAF bin for each sample pair, GenomeStudio project, SNP and samples tables, full SNP technical filter applied, samples reclustered on own data, final reports, PLINK file and README docs explaining the data in each directory

This service level includes:

• Study duplicates at no additional cost
• Full data release, which includes hapmap concordance, reproducibility of genotype calculations broken down by MAF bin for each sample pair, GenomeStudio project, SNP and samples tables, full SNP technical filter applied, samples reclustered on own data, final reports, PLINK file and README docs explaining the data in each directory

We will not supply any controls nor will we redo any samples that fail.  Each sample will be run once in the lab.

This service level includes:

• Study duplicates at no additional cost
• Full data release, which includes hapmap concordance, reproducibility of genotype calculations broken down by MAF bin for each sample pair, GenomeStudio project, SNP and samples tables, full SNP technical filter applied, samples reclustered on own data, final reports, PLINK file and README docs explaining the data in each directory

We will not supply any controls nor will we redo any samples that fail.  Each sample will be run once in the lab.

This service level includes:

• Study duplicates at no additional cost
• idtats, a GenomeStudio project and a PLINK file.  

We will not run a technical filter on your data, so you will need to clean and remove all failed assays from the provided data set.  To visualize and clean the data you will need access to a copy of GenomeStudio from Illumina or similar software from a 3rd party vendor that uses .idat files as input.  Our data release will include the standard .egt file from Illumina, but it will not have been optimized for your specific data.  

You should expect an FTE data analyst to spend at least two weeks cleaning the data after you receive it from us.

This service level includes:

• Study duplicates at no additional cost
• idtats, a GenomeStudio project and a PLINK file.  

We will not run a technical filter on your data, so you will need to clean and remove all failed assays from the provided data set.  To visualize and clean the data you will need access to a copy of GenomeStudio from Illumina or similar software from a 3rd party vendor that uses .idat files as input.  Our data release will include the standard .egt file from Illumina, but it will not have been optimized for your specific data.  

You should expect an FTE data analyst to spend at least two weeks cleaning the data after you receive it from us.

This service level includes:

• Study duplicates at no additional cost
• idtats, a GenomeStudio project and a PLINK file.  

We will not run a technical filter on your data, so you will need to clean and remove all failed assays from the provided data set.  To visualize and clean the data you will need access to a copy of GenomeStudio from Illumina or similar software from a 3rd party vendor that uses .idat files as input.  Our data release will include the standard .egt file from Illumina, but it will not have been optimized for your specific data.  

You should expect an FTE data analyst to spend at least two weeks cleaning the data after you receive it from us.

This service level includes:

• Study duplicates at no additional cost
• idtats, a GenomeStudio project and a PLINK file.  

We will not run a technical filter on your data, so you will need to clean and remove all failed assays from the provided data set.  To visualize and clean the data you will need access to a copy of GenomeStudio from Illumina or similar software from a 3rd party vendor that uses .idat files as input.  Our data release will include the standard .egt file from Illumina, but it will not have been optimized for your specific data.  

You should expect an FTE data analyst to spend at least two weeks cleaning the data after you receive it from us.

This special process repairs highly fragmented DNA (such as from FFPE or CF DNA) so that it is usuable on any Illumina array.

Full service includes:

• Pretesting with the ability to replace/drop poor performing samples
• 2 Controls per plate
• Study duplicates at no additional cost
• Individual sample reruns in the lab for poor performance (repeated 1X)
• Full data release which includes hapmap concordance, reproducibility of genotype calculations broken down by MAF bin for each sample pair, GenomeStudio project, SNP and samples tables, full SNP technical filter applied, samples reclustered on own data, final reports, PLINK file and README docs explaining the data in each directory

Full service includes:

• Pretesting with the ability to replace/drop poor performing samples
• 2 Controls per plate
• Study duplicates at no additional cost
• Individual sample reruns in the lab for poor performance (repeated 1X)
• Full data release which includes hapmap concordance, reproducibility of genotype calculations broken down by MAF bin for each sample pair, GenomeStudio project, SNP and samples tables, full SNP technical filter applied, samples reclustered on own data, final reports, PLINK file and README docs explaining the data in each directory

This service level includes:

• Pretesting with the ability to replace/drop poor performing samples
• Study duplicates at no additional cost
• Full data release, which includes hapmap concordance, reproducibility of genotype calculations broken down by MAF bin for each sample pair, GenomeStudio project, SNP and samples tables, full SNP technical filter applied, samples reclustered on own data, final reports, PLINK file and README docs explaining the data in each directory

We will not supply any controls nor will we redo any samples that fail.  Each sample will be run once in the lab.

This service level includes:

• Study duplicates at no additional cost
• 2 controls per plate
• Individual sample reruns in the lab for poor performance (repeated 1X)
• Full data release, which includes hapmap concordance, reproducibility of genotype calculations broken down by MAF bin for each sample pair, GenomeStudio project, SNP and samples tables, full SNP technical filter applied, samples reclustered on own data, final reports, PLINK file and README docs explaining the data in each directory

Samples will be run as submitted, with no pretesting.

This service level includes:

• Study duplicates at no additional cost
• 2 Controls per plate
• Individual sample reruns in the lab for poor performance (repeated 1X)
• idtats, a GenomeStudio project and a PLINK file.  

We will not run a technical filter on your data, so you will need to clean and remove all failed assays from the provided data set.  To visualize and clean the data you will need access to a copy of GenomeStudio from Illumina or similar software from a 3rd party vendor that uses .idat files as input.  Our data release will include the standard .egt file from Illumina, but it will not have been optimized for your specific data.  

You should expect an FTE data analyst to spend at least two weeks cleaning the data after you receive it from us.

This service level includes:

• Study duplicates at no additional cost
• 2 Controls per plate
• Individual sample reruns in the lab for poor performance (repeated 1X)
• idtats, a GenomeStudio project and a PLINK file.  

We will not run a technical filter on your data, so you will need to clean and remove all failed assays from the provided data set.  To visualize and clean the data you will need access to a copy of GenomeStudio from Illumina or similar software from a 3rd party vendor that uses .idat files as input.  Our data release will include the standard .egt file from Illumina, but it will not have been optimized for your specific data.  

You should expect an FTE data analyst to spend at least two weeks cleaning the data after you receive it from us.

This service level includes:

• Pretesting with the ability to replace/drop poor performing samples
• Study duplicates at no additional cost
• Full data release, which includes hapmap concordance, reproducibility of genotype calculations broken down by MAF bin for each sample pair, GenomeStudio project, SNP and samples tables, full SNP technical filter applied, samples reclustered on own data, final reports, PLINK file and README docs explaining the data in each directory

We will not supply any controls nor will we redo any samples that fail.  Each sample will be run once in the lab.

This service level includes:

• Pretesting with the ability to replace/drop poor performing samples
• Study duplicates at no additional cost
• idtats, a GenomeStudio project and a PLINK file.  

We will not run a technical filter on your data, so you will need to clean and remove all failed assays from the provided data set.  To visualize and clean the data you will need access to a copy of GenomeStudio from Illumina or similar software from a 3rd party vendor that uses .idat files as input.  Our data release will include the standard .egt file from Illumina, but it will not have been optimized for your specific data.  

You should expect an FTE data analyst to spend at least two weeks cleaning the data after you receive it from us.

This service level includes:

• Pretesting with the ability to replace/drop poor performing samples
• Study duplicates at no additional cost
• idtats, a GenomeStudio project and a PLINK file.  

We will not run a technical filter on your data, so you will need to clean and remove all failed assays from the provided data set.  To visualize and clean the data you will need access to a copy of GenomeStudio from Illumina or similar software from a 3rd party vendor that uses .idat files as input.  Our data release will include the standard .egt file from Illumina, but it will not have been optimized for your specific data.  

You should expect an FTE data analyst to spend at least two weeks cleaning the data after you receive it from us.

This service level includes:

• Study duplicates at no additional cost
• Full data release, which includes hapmap concordance, reproducibility of genotype calculations broken down by MAF bin for each sample pair, GenomeStudio project, SNP and samples tables, full SNP technical filter applied, samples reclustered on own data, final reports, PLINK file and README docs explaining the data in each directory

Samples will be run as submitted, with no pretesting.  We will not supply any controls nor will we redo any samples that fail.  Each sample will be run once in the lab.

This service level includes: 

• idtats, a GenomeStudio project and a PLINK file.  

Samples will be run as submitted, with no pretesting.  We will not supply any controls nor will we redo any samples that fail.  Each sample will be run once in the lab.

We will not run a technical filter on your data, so you will need to clean and remove all failed assays from the provided data set.  To visualize and clean the data you will need access to a copy of GenomeStudio from Illumina or similar software from a 3rd party vendor that uses .idat files as input.  Our data release will include the standard .egt file from Illumina, but it will not have been optimized for your specific data.  

You should expect an FTE data analyst to spend at least two weeks cleaning the data after you receive it from us.

This service level includes: 

• idtats, a GenomeStudio project and a PLINK file.  

Samples will be run as submitted, with no pretesting.  We will not supply any controls nor will we redo any samples that fail.  Each sample will be run once in the lab.

We will not run a technical filter on your data, so you will need to clean and remove all failed assays from the provided data set.  To visualize and clean the data you will need access to a copy of GenomeStudio from Illumina or similar software from a 3rd party vendor that uses .idat files as input.  Our data release will include the standard .egt file from Illumina, but it will not have been optimized for your specific data.  

You should expect an FTE data analyst to spend at least two weeks cleaning the data after you receive it from us.

This service level includes:

• Study duplicates at no additional cost
• 2 Controls per plate
• Individual sample reruns in the lab for poor performance (repeated 1X)
• idtats, a GenomeStudio project and a PLINK file.  

We will not run a technical filter on your data, so you will need to clean and remove all failed assays from the provided data set.  To visualize and clean the data you will need access to a copy of GenomeStudio from Illumina or similar software from a 3rd party vendor that uses .idat files as input.  Our data release will include the standard .egt file from Illumina, but it will not have been optimized for your specific data.  

You should expect an FTE data analyst to spend at least two weeks cleaning the data after you receive it from us.

This service level includes:

• Study duplicates at no additional cost
• 2 Controls per plate
• Individual sample reruns in the lab for poor performance (repeated 1X)
• idtats, a GenomeStudio project and a PLINK file.  

We will not run a technical filter on your data, so you will need to clean and remove all failed assays from the provided data set.  To visualize and clean the data you will need access to a copy of GenomeStudio from Illumina or similar software from a 3rd party vendor that uses .idat files as input.  Our data release will include the standard .egt file from Illumina, but it will not have been optimized for your specific data.  

You should expect an FTE data analyst to spend at least two weeks cleaning the data after you receive it from us.

Service for ONT library prep

Service for ONT sequencing.  

Covaris truXTRAC Covaris truXTRAC or Qiagen 

Covaris truXTRAC Covaris truXTRAC or Qiagen 

2 preps, Covaris truXTRAC Covaris truXTRAC or Qiagen 

2 preps, Covaris truXTRAC Covaris truXTRAC or Qiagen 

The processing costs and chip costs are billed separately.  This charge is for the processing costs, which vary depending on the type of chip and number of chips processed. Price shown is for 10 chips, price will be adjusted based on actual number of chips run.

The processing costs and chip costs are billed separately.  This charge is for the processing costs, which vary depending on the type of chip and number of chips processed. Price shown is for 20 chips, price will be adjusted based on actual number of chips run.

Minimum order 10 chips, 144 samples per chip

Minimum order 60 chips, 16 samples/chip

Minimum order 10 chips, 96 samples/chip.

Covaris truXTRAC Covaris truXTRAC or Qiagen 

(~200mm2 for a 5µm section), Covaris truXTRAC or Qiagen 

(~200mm2 for a 5µm section), Covaris truXTRAC or Qiagen 

Covaris truXTRAC Covaris truXTRAC or Qiagen 

Covaris truXTRAC Covaris truXTRAC or Qiagen 

2 preps, Covaris truXTRAC Covaris truXTRAC or Qiagen 

2 preps, Covaris truXTRAC Covaris truXTRAC or Qiagen 

Full service includes:

• Pretesting with the ability to replace/drop poor performing samples
• 2 Controls per plate
• Study duplicates at no additional cost
• Individual sample reruns in the lab for poor performance (repeated 1X)
• Full data release which includes hapmap concordance, reproducibility of genotype calculations broken down by MAF bin for each sample pair, GenomeStudio project, SNP and samples tables, full SNP technical filter applied, samples reclustered on own data, final reports, PLINK file and README docs explaining the data in each directory

Full service includes:

• Pretesting with the ability to replace/drop poor performing samples
• 2 Controls per plate
• Study duplicates at no additional cost
• Individual sample reruns in the lab for poor performance (repeated 1X)
• Full data release which includes hapmap concordance, reproducibility of genotype calculations broken down by MAF bin for each sample pair, GenomeStudio project, SNP and samples tables, full SNP technical filter applied, samples reclustered on own data, final reports, PLINK file and README docs explaining the data in each directory

Full service includes:

• Pretesting with the ability to replace/drop poor performing samples
• 2 Controls per plate
• Study duplicates at no additional cost
• Individual sample reruns in the lab for poor performance (repeated 1X)
• Full data release which includes hapmap concordance, reproducibility of genotype calculations broken down by MAF bin for each sample pair, GenomeStudio project, SNP and samples tables, full SNP technical filter applied, samples reclustered on own data, final reports, PLINK file and README docs explaining the data in each directory

This service level includes:

• Pretesting with the ability to replace/drop poor performing samples
• Study duplicates at no additional cost
• Full data release, which includes hapmap concordance, reproducibility of genotype calculations broken down by MAF bin for each sample pair, GenomeStudio project, SNP and samples tables, full SNP technical filter applied, samples reclustered on own data, final reports, PLINK file and README docs explaining the data in each directory

We will not supply any controls nor will we redo any samples that fail.  Each sample will be run once in the lab.

This service level includes:

• Pretesting with the ability to replace/drop poor performing samples
• Study duplicates at no additional cost
• Full data release, which includes hapmap concordance, reproducibility of genotype calculations broken down by MAF bin for each sample pair, GenomeStudio project, SNP and samples tables, full SNP technical filter applied, samples reclustered on own data, final reports, PLINK file and README docs explaining the data in each directory

We will not supply any controls nor will we redo any samples that fail.  Each sample will be run once in the lab.

This service level includes:

• Pretesting with the ability to replace/drop poor performing samples
• Study duplicates at no additional cost
• idtats, a GenomeStudio project and a PLINK file.  

We will not run a technical filter on your data, so you will need to clean and remove all failed assays from the provided data set.  To visualize and clean the data you will need access to a copy of GenomeStudio from Illumina or similar software from a 3rd party vendor that uses .idat files as input.  Our data release will include the standard .egt file from Illumina, but it will not have been optimized for your specific data.  

You should expect an FTE data analyst to spend at least two weeks cleaning the data after you receive it from us.

This service level includes:

• Pretesting with the ability to replace/drop poor performing samples
• Study duplicates at no additional cost
• idtats, a GenomeStudio project and a PLINK file.  

We will not run a technical filter on your data, so you will need to clean and remove all failed assays from the provided data set.  To visualize and clean the data you will need access to a copy of GenomeStudio from Illumina or similar software from a 3rd party vendor that uses .idat files as input.  Our data release will include the standard .egt file from Illumina, but it will not have been optimized for your specific data.  

You should expect an FTE data analyst to spend at least two weeks cleaning the data after you receive it from us.

This service level includes:

• Study duplicates at no additional cost
• Full data release, which includes hapmap concordance, reproducibility of genotype calculations broken down by MAF bin for each sample pair, GenomeStudio project, SNP and samples tables, full SNP technical filter applied, samples reclustered on own data, final reports, PLINK file and README docs explaining the data in each directory

Samples will be run as submitted, with no pretesting.  We will not supply any controls nor will we redo any samples that fail.  Each sample will be run once in the lab.

This service level includes: 

• idtats, a GenomeStudio project and a PLINK file.  

Samples will be run as submitted, with no pretesting.  We will not supply any controls nor will we redo any samples that fail.  Each sample will be run once in the lab.

We will not run a technical filter on your data, so you will need to clean and remove all failed assays from the provided data set.  To visualize and clean the data you will need access to a copy of GenomeStudio from Illumina or similar software from a 3rd party vendor that uses .idat files as input.  Our data release will include the standard .egt file from Illumina, but it will not have been optimized for your specific data.  

You should expect an FTE data analyst to spend at least two weeks cleaning the data after you receive it from us.

This service level includes: 

• idtats, a GenomeStudio project and a PLINK file.  

Samples will be run as submitted, with no pretesting.  We will not supply any controls nor will we redo any samples that fail.  Each sample will be run once in the lab.

We will not run a technical filter on your data, so you will need to clean and remove all failed assays from the provided data set.  To visualize and clean the data you will need access to a copy of GenomeStudio from Illumina or similar software from a 3rd party vendor that uses .idat files as input.  Our data release will include the standard .egt file from Illumina, but it will not have been optimized for your specific data.  

You should expect an FTE data analyst to spend at least two weeks cleaning the data after you receive it from us.

This service level includes:

• Study duplicates at no additional cost
• 2 controls per plate
• Individual sample reruns in the lab for poor performance (repeated 1X)
• Full data release, which includes hapmap concordance, reproducibility of genotype calculations broken down by MAF bin for each sample pair, GenomeStudio project, SNP and samples tables, full SNP technical filter applied, samples reclustered on own data, final reports, PLINK file and README docs explaining the data in each directory

Samples will be run as submitted, with no pretesting.

This service level includes:

• Study duplicates at no additional cost
• 2 Controls per plate
• Individual sample reruns in the lab for poor performance (repeated 1X)
• idtats, a GenomeStudio project and a PLINK file.  

We will not run a technical filter on your data, so you will need to clean and remove all failed assays from the provided data set.  To visualize and clean the data you will need access to a copy of GenomeStudio from Illumina or similar software from a 3rd party vendor that uses .idat files as input.  Our data release will include the standard .egt file from Illumina, but it will not have been optimized for your specific data.  

You should expect an FTE data analyst to spend at least two weeks cleaning the data after you receive it from us.

This service level includes:

• Study duplicates at no additional cost
• 2 Controls per plate
• Individual sample reruns in the lab for poor performance (repeated 1X)
• idtats, a GenomeStudio project and a PLINK file.  

We will not run a technical filter on your data, so you will need to clean and remove all failed assays from the provided data set.  To visualize and clean the data you will need access to a copy of GenomeStudio from Illumina or similar software from a 3rd party vendor that uses .idat files as input.  Our data release will include the standard .egt file from Illumina, but it will not have been optimized for your specific data.  

You should expect an FTE data analyst to spend at least two weeks cleaning the data after you receive it from us.

This service level includes:

• Study duplicates at no additional cost
• 2 Controls per plate
• Individual sample reruns in the lab for poor performance (repeated 1X)
• idtats, a GenomeStudio project and a PLINK file.  

We will not run a technical filter on your data, so you will need to clean and remove all failed assays from the provided data set.  To visualize and clean the data you will need access to a copy of GenomeStudio from Illumina or similar software from a 3rd party vendor that uses .idat files as input.  Our data release will include the standard .egt file from Illumina, but it will not have been optimized for your specific data.  

You should expect an FTE data analyst to spend at least two weeks cleaning the data after you receive it from us.

This service level includes:

• Study duplicates at no additional cost
• 2 Controls per plate
• Individual sample reruns in the lab for poor performance (repeated 1X)
• idtats, a GenomeStudio project and a PLINK file.  

We will not run a technical filter on your data, so you will need to clean and remove all failed assays from the provided data set.  To visualize and clean the data you will need access to a copy of GenomeStudio from Illumina or similar software from a 3rd party vendor that uses .idat files as input.  Our data release will include the standard .egt file from Illumina, but it will not have been optimized for your specific data.  

You should expect an FTE data analyst to spend at least two weeks cleaning the data after you receive it from us.

Full service includes:

• Pretesting with the ability to replace/drop poor performing samples
• 2 controls per plate
• Study duplicates at no additional cost
• Individual sample reruns in the lab for poor performance (repeated 1X)
• Full data release, which includes hapmap concordance, reproducibility of genotype calculations broken down by MAF bin for each sample pair, GenomeStudio project, SNP and samples tables, full SNP technical filter applied, samples reclustered on own data, final reports, PLINK file and README docs explaining the data in each directory

This service level includes:

• Study duplicates at no additional cost
• 2 controls per plate
• Individual sample reruns in the lab for poor performance (repeated 1X)
• Full data release, which includes hapmap concordance, reproducibility of genotype calculations broken down by MAF bin for each sample pair, GenomeStudio project, SNP and samples tables, full SNP technical filter applied, samples reclustered on own data, final reports, PLINK file and README docs explaining the data in each directory

Samples will be run as submitted, with no pretesting.

This service level includes:

• Pretesting with the ability to replace/drop poor performing samples
• Study duplicates at no additional cost
• Full data release, which includes hapmap concordance, reproducibility of genotype calculations broken down by MAF bin for each sample pair, GenomeStudio project, SNP and samples tables, full SNP technical filter applied, samples reclustered on own data, final reports, PLINK file and README docs explaining the data in each directory

We will not supply any controls nor will we redo any samples that fail.  Each sample will be run once in the lab.

This service level includes:

• Study duplicates at no additional cost
• 2 Controls per plate
• Individual sample reruns in the lab for poor performance (repeated 1X)
• idtats, a GenomeStudio project and a PLINK file.  

We will not run a technical filter on your data, so you will need to clean and remove all failed assays from the provided data set.  To visualize and clean the data you will need access to a copy of GenomeStudio from Illumina or similar software from a 3rd party vendor that uses .idat files as input.  Our data release will include the standard .egt file from Illumina, but it will not have been optimized for your specific data.  

You should expect an FTE data analyst to spend at least two weeks cleaning the data after you receive it from us.

This service level includes:

• Study duplicates at no additional cost
• 2 Controls per plate
• Individual sample reruns in the lab for poor performance (repeated 1X)
• idtats, a GenomeStudio project and a PLINK file.  

We will not run a technical filter on your data, so you will need to clean and remove all failed assays from the provided data set.  To visualize and clean the data you will need access to a copy of GenomeStudio from Illumina or similar software from a 3rd party vendor that uses .idat files as input.  Our data release will include the standard .egt file from Illumina, but it will not have been optimized for your specific data.  

You should expect an FTE data analyst to spend at least two weeks cleaning the data after you receive it from us.

This service level includes:

• 2 controls per plate
• Study duplicates at no additional cost
• Individual sample reruns in the lab for poor performance (repeated 1X)
• Full data release, which includes hapmap concordance, reproducibility of genotype calculations broken down by MAF bin for each sample pair, GenomeStudio project, SNP and samples tables, full SNP technical filter applied, samples reclustered on own data, final reports, PLINK file and README docs explaining the data in each directory

This service level includes:

• 2 controls per plate
• Study duplicates at no additional cost
• Individual sample reruns in the lab for poor performance (repeated 1X)
• Full data release, which includes hapmap concordance, reproducibility of genotype calculations broken down by MAF bin for each sample pair, GenomeStudio project, SNP and samples tables, full SNP technical filter applied, samples reclustered on own data, final reports, PLINK file and README docs explaining the data in each directory

This service level includes:

• Study duplicates at no additional cost
• Full data release, which includes hapmap concordance, reproducibility of genotype calculations broken down by MAF bin for each sample pair, GenomeStudio project, SNP and samples tables, full SNP technical filter applied, samples reclustered on own data, final reports, PLINK file and README docs explaining the data in each directory

We will not supply any controls nor will we redo any samples that fail.  Each sample will be run once in the lab.

This service level includes:

• Study duplicates at no additional cost
• Full data release, which includes hapmap concordance, reproducibility of genotype calculations broken down by MAF bin for each sample pair, GenomeStudio project, SNP and samples tables, full SNP technical filter applied, samples reclustered on own data, final reports, PLINK file and README docs explaining the data in each directory

We will not supply any controls nor will we redo any samples that fail.  Each sample will be run once in the lab.

This service level includes:

• Study duplicates at no additional cost
• idtats, a GenomeStudio project and a PLINK file.  

We will not run a technical filter on your data, so you will need to clean and remove all failed assays from the provided data set.  To visualize and clean the data you will need access to a copy of GenomeStudio from Illumina or similar software from a 3rd party vendor that uses .idat files as input.  Our data release will include the standard .egt file from Illumina, but it will not have been optimized for your specific data.  

You should expect an FTE data analyst to spend at least two weeks cleaning the data after you receive it from us.

This service level includes:

• Study duplicates at no additional cost
• idtats, a GenomeStudio project and a PLINK file.  

We will not run a technical filter on your data, so you will need to clean and remove all failed assays from the provided data set.  To visualize and clean the data you will need access to a copy of GenomeStudio from Illumina or similar software from a 3rd party vendor that uses .idat files as input.  Our data release will include the standard .egt file from Illumina, but it will not have been optimized for your specific data.  

You should expect an FTE data analyst to spend at least two weeks cleaning the data after you receive it from us.

This service level includes:

• Study duplicates at no additional cost
• idtats, a GenomeStudio project and a PLINK file.  

We will not run a technical filter on your data, so you will need to clean and remove all failed assays from the provided data set.  To visualize and clean the data you will need access to a copy of GenomeStudio from Illumina or similar software from a 3rd party vendor that uses .idat files as input.  Our data release will include the standard .egt file from Illumina, but it will not have been optimized for your specific data.  

You should expect an FTE data analyst to spend at least two weeks cleaning the data after you receive it from us.

This service level includes:

• Study duplicates at no additional cost
• idtats, a GenomeStudio project and a PLINK file.  

We will not run a technical filter on your data, so you will need to clean and remove all failed assays from the provided data set.  To visualize and clean the data you will need access to a copy of GenomeStudio from Illumina or similar software from a 3rd party vendor that uses .idat files as input.  Our data release will include the standard .egt file from Illumina, but it will not have been optimized for your specific data.  

You should expect an FTE data analyst to spend at least two weeks cleaning the data after you receive it from us.

This special process repairs highly fragmented DNA (such as from FFPE or CF DNA) so that it is usuable on any Illumina array.

For 8 channel or less pipettes.

For pipettes with 9 or more channels.

Service for ONT library prep

Service for ONT sequencing.  

The processing costs and chip costs are billed separately.  This charge is for the processing costs, which vary depending on the type of chip and number of chips processed. Price shown is for 10 chips, price will be adjusted based on actual number of chips run.

The processing costs and chip costs are billed separately.  This charge is for the processing costs, which vary depending on the type of chip and number of chips processed. Price shown is for 20 chips, price will be adjusted based on actual number of chips run.

Minimum order 10 chips, 144 samples per chip

Minimum order 60 chips, 16 samples/chip

Minimum order 10 chips, 96 samples/chip.