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I am not quite sure about the TOUs but I assume the data is no longer under embargo as of the publication of the paper. |
ahernank
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Apr 24, 2026
| "source": [ | ||
| "## Whole-genome sequencing and variant calling\n", | ||
| "\n", | ||
| "All samples in `Adar1.0` have been sequenced individually to high coverage using Illumina technology at the Wellcome Sanger Institute. These sequence data have then been analysed to identify genetic variants such as single nucleotide polymorphisms (SNPs). After variant calling, both the samples and the variants have been through a range of quality control analyses, to ensure the data are of high quality. Both the raw sequence data and the curated variant calls are openly available for download and analysis. " |
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Can you update this to include:
- A brief description from the methods in the paper
- Point out to the paper with the full methods.
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Same with QC and site filters below, we didn't do bits from there, could we please exclude?
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Update to only to only include data that is currently available & hosted by us.
Co-authored-by: Anastasia Hernandez-Koutoucheva <ah32@sanger.ac.uk>
Co-authored-by: Anastasia Hernandez-Koutoucheva <ah32@sanger.ac.uk>
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Addresses #113 .