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- W2765999819 endingPage "95" @default.
- W2765999819 startingPage "89" @default.
- W2765999819 abstract "In the past decade, chromatin immunoprecipitation sequencing (ChIP-seq) has emerged as the dominant technique for those wishing to perform genome-wide protein:DNA profiling. Owing to the tissue- and cell-type-specific nature of epigenetic marks, the field has been driven towards obtaining data from ever-lower cell numbers. In this review, we focus on the methodological developments that have lowered input requirements and the biological findings they have enabled, as we strive towards the ultimate goal of robust single-cell ChIP-seq." @default.
- W2765999819 created "2017-11-10" @default.
- W2765999819 creator A5001878179 @default.
- W2765999819 creator A5018231357 @default.
- W2765999819 date "2017-10-26" @default.
- W2765999819 modified "2023-09-25" @default.
- W2765999819 title "How low can you go? Pushing the limits of low-input ChIP-seq" @default.
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- W2765999819 doi "https://doi.org/10.1093/bfgp/elx037" @default.
- W2765999819 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/29087438" @default.
- W2765999819 hasPublicationYear "2017" @default.
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