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Since the Spiral_Genetics_insertions.bed file contains only complex insertions, are duplications available?
In case of an insertion, does the third column of the file represent the starting coordinate + the insertion length? That is my guess since, usually, VCF files represent insertions with starting coordinate equal to ending coordinate.
Since in the NA24385 VCF file all variants have SVTYPE equal to DEL or INS, do INS variants include also duplications, or are these only complex insertions?
Thank you very much,
Simone
The text was updated successfully, but these errors were encountered:
In general, I would recommend only using NA24385 as a benchmark for SV calls at this time, since the NA12878 data is a few years old. For NA24385 you should use both the Tier 1 vcf and Tier 1 bed file with truvari to get FPs and FNs, as suggested in the README here:
ftp://ftp-trace.ncbi.nlm.nih.gov/giab/ftp/data/AshkenazimTrio/analysis/NIST_SVs_Integration_v0.6/
Ok, so I can use VCF file in NIST_SVs_Integration_v0.6, even though Truvari documentation says that "This currently only works with GIAB SV v0.5", right?
Thank you very much for the kind information.
On Tue, Dec 11, 2018 at 12:15 PM MaestSi ***@***.***> wrote:
Ok, so I can use VCF file in NIST_SVs_Integration_v0.6, even though
*Truvari* documentation says that "*This currently only works with GIAB
SV v0.5*", right?
Thank you very much for the kind information.
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Dear all,
I would like to use preliminary reference SV calls from GIAB to benchmark some SV calling tools.
For NA24385 sample I am planning to use GIAB VCF file ftp://ftp-trace.ncbi.nlm.nih.gov/giab/ftp/data/AshkenazimTrio/analysis/NIST_SVs_Integration_v0.6/HG002_SVs_Tier1_v0.6.vcf.gz, and maybe I could perform comparisons with some software predictions using Truvari.
While, for NA12878 sample I have found GIAB bed files ftp://ftp-trace.ncbi.nlm.nih.gov/giab/ftp/technical/svclassify_Manuscript/Supplementary_Information/Person
alis_1000_Genomes_deduplicated_deletions.bed and ftp://ftp-trace.ncbi.nih.nlm.gov/giab/ftp/technical/svclassif
y_Manuscript/Supplementary_Information/Spiral_Genetics_insertions.bed.
Since I have no reference VCF file, I think you should use bedtools intersect to make comparisons with my predictions.
My questions are:
Thank you very much,
Simone
The text was updated successfully, but these errors were encountered: