Table 1. Patient and healthy samples analyzed on the Infinium DNA methylation BeadChip.
Disease | Sample ID | Gender | Type | Relation | Status |
---|---|---|---|---|---|
HGP |
AG15694 |
Female |
Immortalized |
Daughter |
Non-mutant |
HGP |
AG15695 |
Female |
Immortalized |
Daughter |
Non-mutant |
HGP |
AG15693 |
Male |
Immortalized |
Father |
Non-mutant |
WS |
AG19911 |
Female |
Immortalized |
None |
LMNA mutant |
WS |
AG03364 |
Male |
Immortalized |
None |
Non-mutant |
WS |
AG07896 |
Female |
Immortalized |
None |
WRN mutant |
WS |
AG11385 |
Male |
Immortalized |
None |
WRN mutant |
PBMC |
PBMC11 |
Male |
Naive |
None |
Healthy donor |
PBMC |
PBMC12 |
Female |
Naive |
None |
Healthy donor |
PBMC |
PBMC14 |
Female |
Naive |
None |
Healthy donor |
LCL |
LCL5 |
Female |
Immortalized |
None |
Healthy donor |
LCL |
LCL6 |
Female |
Immortalized |
None |
Healthy donor |
LCL |
LCL7 |
Female |
Immortalized |
None |
Healthy donor |
B-cells |
Bcell01 |
Female |
Naive |
None |
Healthy donor |
B-cells |
Bcell02 |
Male |
Naive |
None |
Healthy donor |
B-cells | Bcell03 | Male | Naive | None | Healthy donor |
HGP: Hutchinson-Gilford Progeria syndrome; WS: Werner syndrome; LCL: lymphoblastoid cell line, LMNA: lamin A, WRN: Werner syndrome RecQ helicase like.