Table 2.
Genome-wide interrogation goal | Estimated cost per sample |
||
---|---|---|---|
SNP arraya | Next-generation sequencerb | References | |
SNP genotypingc | $700 | $36 000d | (12,13) |
SNP/point mutation discoveryc | NA | $180 000 | (84,85) |
LOH detectione | $1400 | $72 000d | (12,13) |
Copy number assessment | $700 | $2000 | (31,60,82,83) |
Inversion detection | NA | $2000–$180 000f | (82,83) |
Translocation detection | NA | $2000–$180 000f | (82,83) |
aAt flat cost of $700 per array.
bAt $2000 per experiment, each producing 1 Gb of sequence.
cAt 30X coverage for reliable SNP/mutation calling.
dAfter first performing a complexity-reduction step (similar to SNP array protocols) yielding ∼1 M fragments of average size 600 bp.
eUsing both tumor and matched normal DNA samples.
fDepending upon level of resolution desired.
N.B. All costs are very approximate, and will vary with different platforms, economies of scale and other factors.