Common Garden 2b-RAD
Gel extracted 2b-rad PCR samples from Wednesday 10/14/15 using the Qiagen Gel Extraction Kit. Incubated 40 uL of elution buffer on the column for 5 minutes. Decided that going forward I would run PCR product out on a low melt gel and use gelase instead of the kit to save time/money.
Quantified gel extracted samples with High Sensitivity Qubit. Multiplied 37 uL by the lowest concentration to get ng per sample to add to pool, then calculated how many uL of each sample to add to pool. 37 * .373 = 13.8 ng.
| Population | Sample | ng/uL after gel | Vol to add to pool (uL) |
| Oyster Bay | BS_2_6 | 0.907 | 15.21499449 |
| Oyster Bay | BS_2_7 | 0.388 | 35.56701031 |
| Oyster Bay | BS_2_8 | 0.661 | 20.8774584 |
| Hood Canal | BS_1_5 | 0.731 | 18.87824897 |
| Hood Canal | BS_1_6 | 1.45 | 9.517241379 |
| Hood Canal | BS_1_7 | 0.853 | 16.17819461 |
| Hood Canal | BS_1_8 | 0.96 | 14.375 |
| Fidalgo | BS_1_4 | 0.873 | 15.80756014 |
| Fidalgo | BS_1_5 | 0.373 | 36.99731903 |
| Fidalgo | BS_1_6 | 1.07 | 12.89719626 |
GBS Population Structure
Made new annealed adaptors for GBS as the current stock was over 2 years old. Followed Buckler lab protocol. buckler_lab_genotyping_by_sequencing_protocol_20110808
Getting My Genes Wet 
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