Showing: clinvarreset
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Find common entries between VCF and ClinVar VCF
vcf clinvar written 22 days ago by win720 • updated 22 days ago by Sean Davis24k
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VCF mining & interpretation tools (hg38 build)
vcf annotation clinvar snp mining written 5 months ago by elsayedhegazy10 • updated 7 weeks ago by Biostar ♦♦ 20
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How to change snp ID to Variation ID of Clinvar Database
python clinvar snp written 2.1 years ago by cnhuangxy0 • updated 10 months ago by m66110220
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Clinical significance explanation
clinvar clinical significance written 16 months ago by abedkurdi1020 • updated 16 months ago by Devon Ryan76k
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Clinical significance ClinVar
clinvar clinical significance written 18 months ago by onemoreuser0 • updated 18 months ago by Denise - Open Targets4.2k
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ClinVar view from API
clinvar written 18 months ago by win720
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ClinVar local install
clinvar written 22 months ago by win720 • updated 22 months ago by Dan Gaston6.9k
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How to get customized information from OMIM/ClinVar?
clinvar omim snp variants written 2.0 years ago by nkav20 • updated 2.0 years ago by Sean Davis24k
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Find Rare SNPs (dbSNP/clinVar)
clinvar dbsnp snp written 2.4 years ago by jonikuebler0 • updated 2.4 years ago by Dan Gaston6.9k
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is there a Quick way to link variants in a VCF to Genetic Testing Registry
gtr vcf clinvar written 3.0 years ago by Rm7.6k • updated 3.0 years ago by Pierre Lindenbaum104k
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ClinVar download sources
ncbi ftp clinvar snp clinical written 3.3 years ago by Vivek2.0k • updated 3.3 years ago by Sean Davis24k
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ClinVar Mutation representations and Descriptions
representation clinvar variant snp annotation written 3.7 years ago by vigprasud60 • updated 3.6 years ago by nilakshafreezon110
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Finding important predispositions using R
R clinvar read.csv written 3.7 years ago by nilakshafreezon110 • updated 3.7 years ago by Michael Dondrup43k
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