CNV analysis based on the depth of coverage of Illumina data
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Sep 5, 2024 - Python
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gene-panels
Here are 5 public repositories matching this topic...
Human gene annotations for the oncology domain
gene driver-genes annotations cancer-genomics cancer-research functional-annotation oncogenes gene-panels tumor-suppressor-genes
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Jan 16, 2025 - R
Simple perl script to extract mappability from a ROI file
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Sep 24, 2019 - Perl
Integrated analysis of Structural and Copy Number Variants on clinical targeted sequencing data
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Oct 27, 2022 - Perl
GUI coupled to a local database that centralize all NGS variant data and annotations, and to provide powerful filtering tools that are easily accessible to the biologist.
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Jan 13, 2025 - Java
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