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  • Dataset: Whole genome ChIP-seq of histone H3 threonine 11 phosphorylation in Saccharomyces cerevisiae
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  • Summary
  • Conditions

Dataset: Whole genome ChIP-seq of histone H3 threonine 11 phosphorylation in Saccharomyces cerevisiae

External ID
GSE100564
Reference
Kniewel R, et al. (2017)
Channels
1
Conditions
10
Description
We used ChIP-seq to determine the whole-genome enrichment of histone H3 threonine 11 phosphorylation (H3 T11ph) during Saccharomyces cerevisiae meiosis. S. cerevisiae SK1 cells were synchronized for meiotic entry and 3 and 4 hour meiotic samples were obtained. As H3 T11ph is dependent on the formation of meiotic double strand breaks (DSBs), a negative control ChIP-seq sample was obtained from a strain lacking DSBs (spo11-yf). Concurrently, ChIP-seq was carried out for histone H3 as a control for comparision.
Categories
histone modification, DNA replication, recombination and repair

Conditions

Increase the total number of rows showing on this page using the pull-down located below the table, or use the page scroll at the table's top right to browse through the table's pages; use the arrows to the right of a column header to sort by that column; filter the table using the "Filter" box at the top of the table.

ConditionExternal ID
anti-H3 spo11yf 3.5hGSM2686871
anti-H3 T11ph spo11yf 3.5hGSM2686876
anti-H3 T11ph Wild type culture #1 3hGSM2686872
anti-H3 T11ph Wild type culture #1 4hGSM2686873
anti-H3 T11ph Wild type culture #2 3hGSM2686874
anti-H3 T11ph Wild type culture #2 4hGSM2686875
anti-H3 Wild type culture #1 3hGSM2686867
anti-H3 Wild type culture #1 4hGSM2686868
anti-H3 Wild type culture #2 3hGSM2686869
anti-H3 Wild type culture #2 4hGSM2686870
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