Copy number variant caller and depth visualization utility for PacBio HiFi reads
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Oct 22, 2024 - Shell
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cnv
Here are 13 public repositories matching this topic...
eXome Hidden Markov model (XHMM) - Copy Number Variants (CNVs) from Whole Exome Sequencing Data
pipeline ngs next-generation-sequencing duplication pca-analysis pca hidden-markov-model cnv copy-number-variation exomes deletion exome xhmm
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Apr 26, 2017 - Shell
Walk through Red Hat MTV
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Apr 5, 2022 - Shell
Materials & Methods for CNV calling with Genalice software against a benchmark dataset
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Jun 6, 2018 - Shell
Workflow for running PennCNV with Illumina platform final report
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Apr 1, 2019 - Shell
Workflow for running PennCNV with Affymetrix platform files
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Oct 2, 2019 - Shell
A workflow for using SpeedSeq to align and call SVs from WGS data
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Aug 24, 2024 - Shell
Whole genome sequence simulation of DUF1220 domains and testing of alignment strategies
genomics genome simulation alignment cnv copy-number-variation duf1220 alignment-strategies simulating-reads
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Oct 4, 2020 - Shell
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