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updated 6.7 years ago by
igor
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written 6.7 years ago by
Daisy
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It depends on the exact reference used. There is too little information to go off of here, but usually hg19 and GRCh37 are not compatible in annotation operations.
[...] but usually hg19 and GRCh37 are not compatible in annotation
operations.
Do you mean because hg19 (UCSC) prefixed the chromomes with "chr" and GRCh37 not? Otherwise hg19 and GRCh37 should be (nearly) identical for the primary assembly.
That could be a reason why, but the usual reason is that by the time annotation swings by, you're too far invested in one version already. I think there are reasons beyond just the name, but maybe I'm mistaken.
You should spot-check the variants that get successfully annotated (in a genome browser). Do those make sense? That will tell you if the annotation is working properly.
It's possible that all the "dots" you see are non-coding. Depending on how the variants were called, it's possible that most of them are non-coding.
I inspected some, they don't make sense, but don't know how to correct. I can't regenerate the raw vcf, it is old, and we don't have it raw data. But I can change annovar annotations if possible
It depends on the exact reference used. There is too little information to go off of here, but usually hg19 and GRCh37 are not compatible in annotation operations.
so what can be used by annovar that matches build 37? Thanks
Do you mean because hg19 (UCSC) prefixed the chromomes with "chr" and GRCh37 not? Otherwise hg19 and GRCh37 should be (nearly) identical for the primary assembly.
fin swimmer
That could be a reason why, but the usual reason is that by the time annotation swings by, you're too far invested in one version already. I think there are reasons beyond just the name, but maybe I'm mistaken.