--- author: Sam White toc-title: Contents toc-depth: 5 toc-location: left date: 2015-12-19 07:15:06+00:00 layout: post slug: bioanalyzer-bisulfite-treated-olyc-gigas-dna title: Bioanalyzer - Bisulfite-treated Oly/C.gigas DNA categories: - 2015 - BS-seq Libraries for Sequencing at Genewiz - Olympia oyster reciprocal transplant tags: - 1NF11 - 1NF15 - 1NF16 - 1NF17 - 2NF5 - 2NF6 - 2NF7 - 2NF8 - bioanalyzer - Crassostrea gigas - electropherogram - Katherine Silliman - Katie Lotterhos - M2 - M3 - NF2_18 - NF2_6 - olympia oyster - Ostrea lurida - Pacific oyster - RNA Pico 6000 --- Following the guidelines of the [TruSeq DNA Methylation Library Prep Guide (Illumina)(https://github.com/sr320/LabDocs/blob/master/protocols/Commercial_Protocols/Illumina_truseq-dna-methylation-library-prep-guide-15066014-a.pdf), I ran 1μL of each sample on an RNA Pico 6000 chip on the Seeb Lab's Bioanalyzer 2100 (Agilent) to confirm that [bisulfite conversion from earlier today](https://robertslab.github.io/sams-notebook/posts/2015/2015-12-18-bisulfite-treatment-oly-reciprocal-transplant-dna-c-gigas-lotterhos-dna-for-bs-seq/) worked. Results: Data File 1(Bioanlyzer 2100): [2100 expert_Eukaryote Total RNA Pico_DE72902486_2015-12-18_21-05-04.xad](https://eagle.fish.washington.edu/Arabidopsis/Bioanalyzer%20Data/2100%20expert_Eukaryote%20Total%20RNA%20Pico_DE72902486_2015-12-18_21-05-04.xad) Data File 1(Bioanlyzer 2100): [2100 expert_Eukaryote Total RNA Pico_DE72902486_2015-12-18_21-42-55.xad](https://eagle.fish.washington.edu/Arabidopsis/Bioanalyzer%20Data/2100%20expert_Eukaryote%20Total%20RNA%20Pico_DE72902486_2015-12-18_21-42-55.xad) ![](https://eagle.fish.washington.edu/Arabidopsis/20151218_bioanalyzer_RNApico_oly_bisulfite_01.jpg)(http://eagle.fish.washington.edu/Arabidopsis/20151218_bioanalyzer_RNApico_oly_bisulfite_01.jpg) ![](https://eagle.fish.washington.edu/Arabidopsis/20151218_bioanalyzer_RNApico_oly_bisulfite_02.jpg)(http://eagle.fish.washington.edu/Arabidopsis/20151218_bioanalyzer_RNApico_oly_bisulfite_02.jpg) Firstly, the ladder failed to produce any peaks. Not sure why this happened. Possibly not denatured? Seems unlikely, but next time I run the Pico assay, I'll denature the ladder aliquot I use prior to running. Overall, the samples look as they should (see image from TruSeq DNA Methylation Kit manual below), albeit some are a bit lumpy. ![](https://eagle.fish.washington.edu/Arabidopsis/20151218_bioanalyzer_illumina_bisulfite.jpg)(http://eagle.fish.washington.edu/Arabidopsis/20151218_bioanalyzer_illumina_bisulfite.jpg)