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Comparison Between Seq Platforms
Comparison Between Seq Platforms 12-11-26 8:13 PM
Ion Proton vs MiSeq: any suggestion which platform is better? Our
main application is targeted sequencing of cancer panel for clinical
diagnosis.
Shawn Baker ? Allen, as of right now Id say the MiSeq is the better bet.
Its a more established technology than the Proton (which has just been
released) and it seems to be producing higher quality data. But of the Ion
Torrent systems, I would thought the PGM would be a better match than the
Proton for targeted sequencing. Will you need the output of the PI chip
(~10Gb)?
Dale Yuzuki ? Im unafraid admit my bias - Im involved with Marketing the
Ion Proton, for crying out loud - but will chime in here for the case that the
Proton does represent the future, and that depending on the kinds of cancer
panels you are looking at, the future of cancer clinical dx (i.e. whether whole
exomes of tumor/normal pairs become routine), and the sample volume /
turnaround time requirement, it isnt an easy which one is better answer,
rather than which one is better for my present and expected future needs.
A few examples will suffice. Say you want a comprehensive set of cancer-
related genes for a wide-net screening project, a total of over 400 genes
(represented by 16,000 amplicons). (Heres a link to the product flyer for
reference:/content/sfs/brochures/Ion_CompCan
cerPanel_Flyer.pdf) A 318 run can do about 350x coverage of a single
sample, but a PI chip on the Proton could do multiple samples in a single 4-
hour run.
The MiSeq, by comparison, would have about the same coverage (doing
2x150bp reads) on the same target size (say using their TruSeq Custom
Amplicon as they dont have an equivalent panel).2x250 reads wont help, as
the insert size of the targets are too small, and would take about 27h for the
run to finish.
If you would then price out the relative sequencing costs, for the PGM 318
that would be a bit over $1,000 for a single sample, the MiSeq
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