BackgroundThe barcoding of next generation sequencing libraries has become an essential part of the experimental design. Barcoding not only allows the sequencing of more than one sample per lane, but also reduces technical bias. However, current barcoding strategies impose significant limitations and/or technical barriers in their implementation for ChIP-sequencing.FindingsConverting Y-shaped sequencing adapters to double stranded DNA prior to agarose gel size selection reduces adapter dimer contamination and quantitating the number of cycles required for amplification of the library with qPCR prior to library amplification eliminates library over-amplification.ConclusionsWe describe an efficient and cost effective method for making barcoded ChIP-seq libraries for sequencing on the Illumina platform.
A method for generating highly multiplexed ChIP-seq libraries
E. Ford,Chrysa Nikopoulou,Antonis Kokkalis,D. Thanos
Published 2014 in BMC Research Notes
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- Publication year
2014
- Venue
BMC Research Notes
- Publication date
2014-05-22
- Fields of study
Biology, Medicine
- Identifiers
- External record
- Source metadata
Semantic Scholar, PubMed
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