Abstract
Different ChIP-Seq protocolsmay 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.
| Lingua originale | Inglese |
|---|---|
| pagine (da-a) | 156-162 |
| Numero di pagine | 7 |
| Rivista | Briefings in Functional Genomics |
| Volume | 14 |
| DOI | |
| Stato di pubblicazione | Pubblicato - 2015 |
Keywords
- Algorithms
- Animals
- Biochemistry
- Bioinformatics analysis
- Brain Stem
- ChIP-Seq
- Chromatin Immunoprecipitation
- Chromatin immunoprecipitation
- Computational Biology
- DNA
- Electrophoresis, Gel, Two-Dimensional
- Genetics
- Mice
- Molecular Biology
- Next-generation sequencing
- Sequence Analysis, DNA
- Statistics as Topic
- Two-dimensional strandness-dependent electrophoresis
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