deepBreaks , a computational method, aims to identify important changes in association with the phenotype of interest using multi-alignment sequencing data from a population.
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Updated
Aug 15, 2024 - Jupyter Notebook
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phenotype-genotype-information
Here are 5 public repositories matching this topic...
Web tool for visualizing phenotype-similarity gene networks
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Dec 10, 2024 - Jupyter Notebook
Indonesia Exome Rare Disease Variant Discovery Pipeline. Phenotype analysis part available on Streamlit and PyPi
gene-prioritization phenotype-exchange-format phenotype-ontologies exome-sequencing-analysis rare-variant-analysis phenotype-prediction rare-disease phenotype-genotype-information
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Aug 6, 2024 - Jupyter Notebook
IdeRare Phenotype Analysis suite : Convert Indonesia SATUSEHAT terminology (SNOMED-CT, LOINC, ICD-10) to Rare Disease Terminology / Ontology (HPO, OMIM) and find the likelihood differential gene and disease explaining patient phenotype
phenotype phenotype-exchange-format phenotype-ontologies phenotype-prediction rare-disease phenotype-genotype-information
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Dec 23, 2024 - Jupyter Notebook
Repository for the ancestry analysis of essential genes in eukaryotes
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Jun 2, 2021 - R
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