Paper Details

Paper Title

aRgus: Multilevel visualization of non-synonymous single nucleotide variants & advanced pathogenicity score modeling for genetic vulnerability assessment.

Paper Journal Title

Comput Struct Biotechnol J

Paper Citation Count

Paper Publication Year

2023

Bio Mention

ClinVar, amino acid, candidate genes, chromosomal exon-intron structure, gene, gnomAD variant, human, human genome, non-synonymous single nucleotide variants, protein regions

Mesh Descriptor

Author Name	Affiliation
Sebastian Uhrig	National Center for Tumor Diseases (NCT), German Cancer Research Center (DKFZ)
Daniel H??bschmann	National Center for Tumor Diseases (NCT), German Cancer Research Center (DKFZ)
Daniel H??bschmann
Daniel H??bschmann	Heidelberg Institute for Stem Cell Technology and Experimental Medicine (HI-STEM)
Daniel H??bschmann	National Center for Tumor Diseases (NCT), German Cancer Research Center (DKFZ)
Daniel H??bschmann
Daniel H??bschmann	Heidelberg Institute for Stem Cell Technology and Experimental Medicine (HI-STEM)

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Dataset	Description	Source Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link

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