cnv
Here are 90 public repositories matching this topic...
eXome Hidden Markov model (XHMM) - Copy Number Variants (CNVs) from Whole Exome Sequencing Data
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Apr 26, 2017 - Shell
A fork of the project Excavator2 from sourceforge.
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Jun 29, 2017 - R
Copy number estimation of highly duplicated sequences
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Aug 15, 2017 - Perl
Epicopy R package for CNV identification from methylation microarrays.
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Sep 19, 2017 - R
A tool to call CNV (Copy Number Variation) from bulk ATAC-Seq data
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Jun 4, 2018 - R
Materials & Methods for CNV calling with Genalice software against a benchmark dataset
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Jun 6, 2018 - Shell
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Aug 17, 2018 - R
Short reads aligner for NIPT/CNV
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Oct 10, 2018 - C
Workflow for running PennCNV with Illumina platform final report
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Apr 1, 2019 - Shell
Inference of subclonal populations in cancer genomes using smoothing splines
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Apr 11, 2019
X11 related utilities for hts
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May 10, 2019 - C++
Using Convolutional Neural Networks to model an association between a genomic sequence and the number of sequenced reads that align to it
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Jul 18, 2019 - Jupyter Notebook
Workflow for running PennCNV with Affymetrix platform files
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Oct 2, 2019 - Shell
This is a group project
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Nov 15, 2019 - R
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