I am unsure as to whether my already extracted DNA is of a high enough quality for SeqSNP. If I submit my samples, and they are of suboptimal quality, will I be notified? learn more
How much DNA do I need to run on an agarose gel to initially assess whether my DNA is suitable for SeqSNP? learn more
I wish to screen F2 segregating populations in which each SNP can be both homozygous and heterozygous. Will SeqSNP provide enough depth of coverage to allow for this level of discrimination? learn more
When sending plant samples for extraction and sequencing, can I send the samples in a deep well plate? learn more
I have some historic leaf punch samples which I stored at -20 °C without any buffer (due to buffer salt crystallisation on thawing). Would it be possible to send these leaf punches to LGC Biosearch Technologies for extraction and sequencing? learn more
I have a lower-than-recommended concentration of DNA. Can I perform whole genome amplification (WGA) on my DNA prior to submitting it for SeqSNP? learn more
For my SeqSNP project, can I submit my DNA in both 96-well plate and 384-well plate format? learn more
I have already sent primary samples/DNA to LGC, Biosearch Technologies for an all-inclusive project/sequencing project in the past. Can these samples be used for SeqSNP? learn more
I have a combination of both extracted DNA and primary samples for extraction for a single SeqSNP project. Can I submit both DNA and primary samples? learn more
I have limited amounts of DNA remaining for my project. What is the minimum DNA concentration I can submit without impacting library preparation too much? learn more
I wish to submit regular samples for the same markers over an extended period of time. How will this affect the expected turnaround times? learn more
