Different cell lines have different data qualities and resolutions as well
DNA labeling: BrdU vs EdU. PFA Fixation affects the map
Quality controls list
Variation in sized in a typical experiment (for QC)
2.- Processing E/L method
Shape recognition for “ripples”, are those discontinuities in replication domains?
To what extent the resolution is limited by cell-to-cell variation instead of technology. Combination of single cells experiments are needed
3. Repli-chip vs Repli-seq
In most of the cases Repli-chip is adequate but not all cases.
4. Repli-seq biases and QC
Are there additional information that will be useful to evaluate Repli-seq data? Those data can be included when depositing Repli-seq data. A second session can be scheduled to discuss about these.
4dn/phase1/omicswg/minutes-03-13-2017.1550254760.txt.gz · Last modified: 2025/04/22 16:21 (external edit)