Software

CaraVaN python script

Monash University
Gulrez Chahal (Aggregated by) Mirana Ramialison (Aggregated by) Sonika Tyagi (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:doi10.26180/15057237.v2&rft.title=CaraVaN python script&rft.identifier=https://doi.org/10.26180/15057237.v2&rft.publisher=Monash University&rft.description=This is the CaraVaN script based on XGBoost method to prioritise potential pathogenic variants in Congenital heart disease and related heart diseases. This script is modification of ncER tool (https://github.com/TelentiLab/ncER_datasets) for cardiac utility.&rft.creator=Gulrez Chahal&rft.creator=Mirana Ramialison&rft.creator=Sonika Tyagi&rft.date=2021&rft_rights=CC-BY-4.0&rft_subject=Congenital Heart Diseases&rft_subject=heart disease&rft_subject=bioinformatics analyses&rft_subject=variant prioritization pipelines&rft_subject=non-coding genomic sequences&rft_subject=Bioinformatics&rft_subject=Health Informatics&rft_subject=Bioinformatics Software&rft.type=Computer Program&rft.language=English Access the software
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CC-BY

CC-BY-4.0

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This is the CaraVaN script based on XGBoost method to prioritise potential pathogenic variants in Congenital heart disease and related heart diseases. This script is modification of ncER tool (https://github.com/TelentiLab/ncER_datasets) for cardiac utility.

Issued: 2021-07-27

Created: 2021-07-27

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Subjects
Bioinformatics | Bioinformatics Software | Congenital Heart Diseases | Health Informatics | bioinformatics analyses | heart disease | non-coding genomic sequences | variant prioritization pipelines |

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