You signed in with another tab or window. Reload to refresh your session.You signed out in another tab or window. Reload to refresh your session.You switched accounts on another tab or window. Reload to refresh your session.Dismiss alert
What's the general guidance for generating PFB files for a multi ancestry cohort that is genotyped? How should generation of PFB files (or PennCNV) be approached alternatively for a multi-ancestry cohort..compared to a cohort of uniform ancestry..Thanks.
The text was updated successfully, but these errors were encountered:
In practice the actual PFB values have minor influence on CNV calling.
So it is totally fine to use multi-ancestry cohort to build PFB files,
which actually increase the likelihood of polymorphic alleles.
This allows more unbiased comparison of CNV calls on multiple cohorts, when
using the same PFB file for CNV calling.
On Sun, Feb 14, 2021 at 6:01 AM psychrb ***@***.***> wrote:
What's the general guidance for generating PFB files for a multi ancestry
cohort that is genotyped? How should generation of PFB files (or PennCNV)
be approached alternatively for a multi-ancestry cohort..compared to a
cohort of uniform ancestry..Thanks.
—
You are receiving this because you are subscribed to this thread.
Reply to this email directly, view it on GitHub
<#68>, or unsubscribe
<https://github.com/notifications/unsubscribe-auth/ABNG3OAGYGWGZA3SYI3ZLZTS66UQLANCNFSM4XTDWRVA>
.
What's the general guidance for generating PFB files for a multi ancestry cohort that is genotyped? How should generation of PFB files (or PennCNV) be approached alternatively for a multi-ancestry cohort..compared to a cohort of uniform ancestry..Thanks.
The text was updated successfully, but these errors were encountered: