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SFHS_pedigrees

Deep (>25x mean coverage) whole genome sequencing on 5-10 families drawn from the Scottish Family Health Study with four or more children.

Click on a Dataset ID in the table below to learn more, and to find out who to contact about access to these data

Dataset ID Description Technology Samples
EGAD00001001214 Illumina HiSeq 2000 19
EGAD00001003211 HiSeq X Ten 57
Publications Citations
Timing, rates and spectra of human germline mutation.
Nat Genet 48: 2016 126-133
270
Similarities and differences in patterns of germline mutation between mice and humans.
Nat Commun 10: 2019 4053
43