Abstract
Different ChIP-Seq protocols may have a significant impact on the final outcome in terms of quality, number and distribution of called peaks. Sample DNA undergoes a long procedure before the final sequencing step, and damaged DNA can result in excessive mismatches in the alignment with reference genome. In this letter, we present the effect of well-defined modifications (timing of formaldehyde crosslink reversal, brand of the sonicator) of standard ChIP-Seq protocol on parallel samples derived from the same cell line correlating the initial DNA quality control metrics to the final bioinformatics analysis results.
| Original language | English |
|---|---|
| Pages (from-to) | N/A-N/A |
| Journal | Briefings in Functional Genomics |
| DOIs | |
| Publication status | Published - 2014 |
Keywords
- ChIP-Seq
- bioinformatics analysis
- chromatin immunoprecipitation
- next-generation sequencing
- two-dimensional strandness-dependent electrophoresis
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