I’m working on a ddRADseq project. We are planning to sequence 2,800 individual lizards from a closed island population. Our plan is to use 48 separate inline barcodes and 59 pcr indices to identify individual samples. We digested with EcoRI and SphI and after size selection expect 7-8,000 fragments per individual. The current plan is to combine samples from all 2,800 individuals into a single pool and sequence all individuals in each HiSeq lane. We will then run as many lanes of sequencing as needed to attain desired coverage (~20x)?
Does pooling this number of individuals seem reasonable to people with experience on ddRAD projects with large numbers of samples?
Does pooling this number of individuals seem reasonable to people with experience on ddRAD projects with large numbers of samples?
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