FHIR Chat · Tracking WES data · implementers

Stream: implementers

Topic: Tracking WES data


view this post on Zulip Damien Jones (Jun 23 2020 at 20:54):

Hi All,
Forgive me if something like this has already been dealt with, I tried searching and didn't see anything obvious. We're trying to capture all the data generated by whole exome sequencing.

From a sample we get this data: raw reads (fastq files), an aligned genome (bam file), and variants (vcf files).

Are Observations appropriate for tracking these files? Would it make sense to bundle them in a Component?

Any guidance would be welcome.

Thanks.

view this post on Zulip Lloyd McKenzie (Jun 23 2020 at 21:21):

I'd recommend re-asking on the #genomics stream

view this post on Zulip Damien Jones (Jun 23 2020 at 21:55):

I'll do that, thanks


Last updated: Apr 12 2022 at 19:14 UTC