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Merge pull request #8 from mellybelly/patch-1
Update requirements.md
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requirements.md

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@@ -43,6 +43,7 @@ fields optional unless explicitly stated:
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* age of onset of disease
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* 1 to N positive phenotype associations for each person - REQUIRED
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* 0 to M negative phenotype associations for each person
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* Variants in HGVS notation, confirmed or set of variants
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TBD: is this sufficient? Below are some additional complex attributes.
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Note that if these are included in the format, then the complexity
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### Siblings/Cohorts
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From M: "be able to represent patients, siblings, and cohorts"
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Represent more than one patient, which could include siblings, parents, and other members of a cohort.
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What does this mean? Represent relationships between them? Or is the
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requirement simply that more than one human can be included in a
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submission?
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I assume the latter. Note for relationships between the individuals,
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the ped file would be used. TODO: investigate who identifiability is
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Note for relationships between the individuals, the ped file would be included. TODO: investigate who identifiability is
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handled in a ped file, as this will impact how we use id fields.
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