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JSU Bioinformatics
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0:09:54
The NCBI Minute: Find All Variants with ClinVar
0:08:51
How to Search ClinVar
0:12:41
Using ClinVar: what it is, why it matters, and how to incorporate it into your variant reviews
0:00:39
ClinVar Reaches One Million Variants!
0:42:12
Webinar: MedGen, GTR, and Clinvar
0:00:39
(Audio Described Version) ClinVar Reaches One Million Variants!
0:16:03
The NCBI Minute: The New ClinVar Submission Wizard
0:06:26
Search ClinVar with Ease
0:39:46
Presentation - Use of and Submission to ClinVar (Melissa Landrum)
0:45:43
Using ClinVar - For the ClinGen Biocurator Working Group
0:34:46
ClinVar Miner
0:19:20
ClinGen and ClinVar: Complementary resources - Erin Riggs
0:23:10
ClinVar Data: Current Limitations for Germline Variants | Center for Genomic Interpretation | Oct&ap...
0:33:11
Using NCBI Data with Tools that Predict the Functional Impact of Genomic Variants
0:20:01
Panel 2: Consistency of Interpretation of Variants Across Expert Labs/Groups, ClinVar Submissions
0:06:37
Clinvar
1:00:23
Using Mastermind’s New ClinVar Integration to Accelerate Clinical Diagnoses
0:03:23
ASHG 2018 - Jennifer Poitras on QCI concordance with ClinVar
0:05:09
Understanding Variant Interpretation Discrepancy in ClinVar [Part 1]
0:01:21
ClinVar 10th Anniversary
0:01:43
Introducing the ClinVar Submission API
0:20:47
Genomic Medicine X: ClinGen and ClinVar - Heidi Rehm
0:05:32
What is ClinVar? A database for variant interpretation! [Today's paper]
0:45:38
GenomeConnect and ClinVar Webinar