Illumina Technology

User Guide

The instructions in this guide must be followed carefully to achieve the best possible results and avoid delays in processing your request.

Any samples that do not comply with the recommendations may be rejected without compensation.

Note that delays in the processing of libraries will vary depending on the size of the project. It is recommended to contact the Client Management Office for information regarding processing time.

Genomic DNA is usually the material used for all protocols except the circulating DNA protocol. If the starting material is different, you must contact a member of the Client Management Office to discuss feasibility.

Practical advice and good laboratory practices
  • Samples should exhibit the highest possible quality and purity. Quality is not assessed at the CES; only quantification is performed
  • DNA concentration should be measured using fluorometric methods (e.g., Qubit, PicoGreen) rather than spectrophotometric methods (e.g., Nanodrop), which tend to overestimate sample concentration and may result in an inadequate amount of starting material.
  • DNA should be extracted using commercial kits rather than homemade solutions.
  • If Trizol is used to extract DNA samples, a final cleanup should be performed (e.g., using a column‑based cleanup kit) before submitting the samples.
  • Samples should be treated with RNase to eliminate the possibility of RNA contamination.
  • DNA should be resuspended in 10 mM Tris‑HCl pH 8.0; 0.1 mM EDTA, in commercial RNase/DNase‑free water, or in the elution buffer provided in commercial kits.
  • Samples should not contain insoluble material, RNA, chelating agents (e.g., EDTA), divalent cations, phenol, detergents, or contaminants originating from the source material (organism or tissue).
Library preparation typeQuantityConcentrationVolumeQuality
Shotgun with PCR≥150ng≥5 ng/µL≥30 µLRatio 260:280 1.8-2.0 Ratio 260:230 ≥2.0
PCR Free Shotgun≥600ng≥20 ng/µL≥30 µLRatio 260:280 1.8-2.0 Ratio 260:230 ≥2.0
Methyl-seq≥150 ng≥5 ng/µL≥30 µLRatio 260:280 1.8-2.0 Ratio 260:230 ≥2.0
Whole Exome (Agilent SureSelect Probes)≥150 ng≥5 ng/µL≥30 µLRatio 260:280 1.8-2.0 Ratio 260:230 ≥2.0
Whole Exome (Roche KAPA HyperExome Probes)≥150 ng≥5 ng/µL≥30 µLRatio 260:280 1.8-2.0 Ratio 260:230 ≥2.0
cfDNA libraries≥30 ng≥1 ng/µL≥30 µLRatio 260:280 1.8-2.0 Ratio 260:230 ≥2.0
Replacement samples are accepted and must meet the same criteria as the original samples. Partial replacements (‘top‑ups’) are not accepted.
  • Samples must be sent in 96‑well plates, regardless of the number of samples
  • Each plate must contain only samples belonging to a single Nanuq project. 
  • Each plate must be clearly identified, and the samples must be placed exactly as indicated in the sample submission form.
Accepted FormatsUnaccepted Formats
Recommanded full skirt plates :

– BioRad Hard-Shell 96-Well PCR Plates, skirted, Cat# HSP9601               
– Eppendorf twin.tec, Cat# 951020401 
– Corning Thermowell GOLD, Cat# 3752 
– Half-skirt plates
– Non skirted plates
– Cell culture plates
Recommanded adhesive films
 
– Life Technologies MicroAmp® Clear Adhesive Film, Cat# 4306311
– Thermo Scientific™ Adhesive PCR Plate Seals, Cat# AB0558
– VWR Aluminum Foils for PCR and Cold Storage, Cat# 60941-074
 

Click on request a service and submit samples to view the instructions.

Click on Samples shipment preparation to view the instructions.

A message is sent to all contact persons listed in the Nanuq project as soon as the results of the initial sample quality control are available. The same applies when the library quality control results become available

An automated notification from Nanuq will be sent to the principal investigator and project contacts once sequencing data are available.

Sequencing results are directly accessible via the Nanuq web application.

For more information on downloading data and available files, please refer to the Frequently Asked Questions page.

Version 2.0_2026-04-21