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Frequently asked questions
Our Scientific Applications Support team has assembled a list of frequently asked questions to help you find answers quickly. Filter using one or more categories to focus on specific topics, or use the search bar to perform a text search.
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How do I analyze CRISPR-editing next generation sequencing (NGS) data with the rhAmpSeq™ CRISPR Analysis Tool?
For compatibility with the rhAmpSeq CRISPR Analysis Tool, we recommend submitting the targets of interest to the rhAmpSeq Design Tool as a 6-column BED file that includes the following information: chromosome, start, stop, desired name, mismatch # (or a 0), and strand (+ or –).
You can use the rhAmpSeq CRISPR Analysis Tool user guide for further information about input file formatting.
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