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. 2010 Jan 7;38(7):2168–2176. doi: 10.1093/nar/gkp1204

Table 1.

Data sets used in this study

ID Platform Number regular probes Number negative controls Experiment description
1 MouseWG-6 V1.1 46 657 1603 Six cell types: hematopoietic stem cells, CMPs, GMPs, pro DC precursors, neutrophils and macrophages. Number of arrays per cell type: 4, 2, 1, 3, 1 and 3, respectively.
2 MouseWG-6 V1.1 46 657 1603 Two cell types: wild type and Aire knockout MHCIIhi mTECs. Number of arrays per cell type: 3.
3 MouseWG-6 V2 45 281 936 Three cell types: pro DC precursors, neutrophils and macrophages. Number of arrays per cell type: 9, 3 and 3, respectively.
4 MouseWG-6 V2 45 281 936 Four cell types: hematopoietic stem cells, CMPs, GMPs and MEPs. Number of arrays per cell type: 3.
5 HumanWG-6 V1 47 312 1517 Six conditions: MCF7 and Jurkat samples were mixed at six different proportions (see Figure 4a). Number of arrays per condition: 2.
6 HumanWG-6 V1 47 312 1517 Four conditions: Universal Human Reference RNA(UHRR) and Human Brain Reference RNA(HBRR) were mixed at four different proportions (see Figure 4b). Number of arrays per condition: 5. Published in ref. (15)
7 HumanWG-6 V2 48 687 1374 Six conditions: three subtypes of T lymphocytes taken from two patients infected with hepatitis C virus. Number of arrays per condition: 1. Published in ref. (16)
8 HumanHT-12 48 799 759 Twelve samples. Bone marrow from seven malaria-infected and five uninfected donors. Number of arrays per sample: 1.
9 HumanWG-6 V3 48 803 759 Four cell types: LinCD49fhiEpCAM, LinCD49fEpCAM, LinCD49fEpCAM+ and LinCD49f+EpCAM+ mammary subpopulations. Number of arrays per cell type: 3. Published in ref. (17)