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• Can I buy a DNA sequencer from SEQme?
• Which qPCR instruments do you provide training for?
• You offer refurbished sequencers, what exactly does that mean?
• I am interested in qPCR courses but there are no dates announced, what to do?
• Why do you offer refurbished sequencers only and not new ones?
• I want to register for your course as a private person, how can I do this?
• I got lost which sequencer to choose, please advice!
• Can I ask you to optimize my qPCR primers and probes?
• Can I buy a new sequencer Applied Biosystems® 310 or 3130/xl?
• How do I order Next-Generation Sequencing?
• How do I order Sanger sequencing or Fragment analysis?
• Why should I choose SEQme as an instrument or service provider?
• Can I run the Applied Biosystems® 310 sequencer with the newer OS than Windows XP?
• Why should I upgrade the Applied Biosystems® 310 sequencer to Windows 10?
• Can you also upgrade Applied Biosystems® 3130/xl sequencers to Windows 10?
• General rules of sample preparation
• Sample submission guidelines
• What are the electrical requirements when installing sequencers 3130 or 3130xl?
• Is it necessary to air-condition the room where the sequencer is installed?
• How do I ship samples?
• Do you recommend using other then original reagents and consumables, i.e. capillaries, polymers, buffers etc.?
• Guidelines for Ready-to-Run libraries (Illumina only)
• Guidelines for sample preparation for DNA metabarcoding - Tailed-amplicon sequencing (Illumina only)
• Additional sample submission guidelines - PacBio sequencing
• Additional sample submission guidelines - Oxford Nanopore sequencing
• StandardSeq – Preparation of samples
• Sample shipment guidelines
• RapidSeq - Preparation of samples
• ColonySeq – Preparation of samples
• CleanSeq – Preparation of samples
• HairpinSeq – Preparation of samples
• What is the difference between sequencing protocols you offer?
• How are RapidSeq protocol results evaluated?
• Fragment analysis – Preparation of samples
• Can I copy-paste into the order form?
• How do I measure DNA/RNA concentration?
• Universal primers
• My own primers
• What primers do you use for taxonomic analysis (based on 16S rDNA gene and other regions)?
• How should I specify primer sequences?
• I want to use my own primer which you use as a universal primer, how can I do this?
• How should I specify the template size?
• There is a limit on template length in the order form for Sanger sequencing. Why?
• Can I copy-paste into the NGS order form?
• Which fields in order forms are compulsory?
• Must I print and send the order confirmation together with samples?
• Should I provide any specific data about my samples when submitting NGS order?
• What sequencing capacity should I allocate?
• I cannot send the online order
• What data will I receive after my sequencing experiment has been finished?
• Can you guarantee what amount of NGS sequencing data I will get?
• Where and how long do you store my results?
• What happens with my NGS samples in SEQme lab?
• What if my NGS samples do not pass quality control in SEQme lab?
• Will the data I finally get be analyzed?
• Where and how long do you store my NGS results?
• Subscribing sequencing services
• Subscribing sequencing services