Data

CaraVaN score for non-coding variants in Chr12 (GRCh38)

Monash University
Gulrez Chahal (Aggregated by)
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ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Adc&rfr_id=info%3Asid%2FANDS&rft_id=info:doi10.26180/15057870.v1&rft.title=CaraVaN score for non-coding variants in Chr12 (GRCh38)&rft.identifier=https://doi.org/10.26180/15057870.v1&rft.publisher=Monash University&rft.description=This data presents CaraVaN score for cardiac pathogenicity of non-coding variants in Chr 12 on a scale of 0-1 where 0 is the least pathogenic to 1 as highly pathogenic. &rft.creator=Gulrez Chahal&rft.date=2021&rft_rights=CC-BY-4.0&rft_subject=Variant prioritisation&rft_subject=Congenital Heart Diseases&rft_subject=heart disease&rft_subject=bioinformatic methodology&rft_subject=machine learning-based&rft_subject=Bioinformatics&rft_subject=Health Informatics&rft_subject=Bioinformatics Software&rft.type=dataset&rft.language=English Access the data
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This data presents CaraVaN score for cardiac pathogenicity of non-coding variants in Chr 12 on a scale of 0-1 where 0 is the least pathogenic to 1 as highly pathogenic.

Issued: 2021-07-27

Created: 2021-07-27

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Subjects
Bioinformatics | Bioinformatics Software | Congenital Heart Diseases | Health Informatics | Variant prioritisation | bioinformatic methodology | heart disease | machine learning-based |

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