Get Brown University Genomics Core Next Generation Sample ...

This guide provides a clear and supportive approach to completing the Brown University Genomics Core Next Generation Sample Sequencing Form online. By following the steps outlined below, users can ensure accurate and efficient submission of their information.

Follow the steps to successfully complete the form.

1. Click ‘Get Form’ button to obtain the form and open it in the editor.
2. Begin by filling out the customer information section. Input your principal investigator (PI) name, institution, email address, department, grant number, and phone number as required.
3. Select the sample type by marking the appropriate checkbox from the options provided, including gDNA, small RNA, PCR amplicon, mRNA, cDNA, ChIP, or other. If you choose 'other', please specify.
4. Provide the source organism's name in the designated field, and input the purification method used.
5. Indicate the concentration measurement method by checking one of the options: Nanodrop, PicoGreen, bioanalyzer, or other. If other, please specify.
6. For requested experiments, select the applicable services, such as library preparation, clustering and sequencing, single read, or paired end.
7. Select the desired run length by marking one of the provided options: 35 bp, 50 bp, 75 bp, or 100 bp.
8. Proceed to the sample information section and fill in the sample name, concentration (ng/µL), A260/A280, volume (µL), and total DNA (µg) for each sample listed (up to eight samples).
9. If available, attach an image of an EtBr-stained 2% agarose gel or E-gel showing 1 µL of each sample, with a 1 kb ladder as a reference. Clearly indicate sample identity in each lane.
10. Once all fields are completed, finalize your submission process. You can save changes, download, print, or share the form as needed.

Complete your Brown University Genomics Core Next Generation Sample Sequencing Form online today.