This folder includes simulated and real data used in validating CNETML, a new maximum likelihood method designed to reconstruct the evolutionary history of multiple samples of a single patient which may be taken at different locations and/or times, which can take as input (relative) total integer copy numbers called from shallow whole genome sequencing data
Summary:Copy number variation is an important and abundant source of variation in the human genome, ...
Received on; revised on; accepted on Motivation: DNA copy number variants (CNV) are gains and losses...
Copy number variation (CNV) is a prevalent form of critical genetic variation that leads to an abnor...
This folder includes simulated and real data used in validating CNETML, a new maximum likelihood met...
This folder includes the source code for CNETML v1.0 (https://github.com/ucl-cssb/cneta), a new maxi...
Recent advances in sequencing technologies provide the means for identifying copy number variation (...
Maximum likelihood phylogeny generated using partitioned analysis in RAxML for 309 species, includin...
Maximum likelihood phylogeny generated via RAxML and associated nonparametric bootstrap replicates f...
Recent advances in genomics have underscored the surprising ubiquity of DNA copy number variants (CN...
Maximum likelihood phylogeny generated using partitioned analysis in RAxML for 164 species
The CNest methods allow large scale CNV detection from very large WGS and WES datasets and generates...
Background Detection of copy number variation (CNV) in genes associated with disease is important in...
<p>The core genome phylogeny obtained by the maximum-likelihood method with x100 bootstrapping.</p
Copy number variation (CNV) is a type of genomic structural variation which has been associated with...
Analyses were based on full genomic sequences (i.e. including both variant and invariant sites)
Summary:Copy number variation is an important and abundant source of variation in the human genome, ...
Received on; revised on; accepted on Motivation: DNA copy number variants (CNV) are gains and losses...
Copy number variation (CNV) is a prevalent form of critical genetic variation that leads to an abnor...
This folder includes simulated and real data used in validating CNETML, a new maximum likelihood met...
This folder includes the source code for CNETML v1.0 (https://github.com/ucl-cssb/cneta), a new maxi...
Recent advances in sequencing technologies provide the means for identifying copy number variation (...
Maximum likelihood phylogeny generated using partitioned analysis in RAxML for 309 species, includin...
Maximum likelihood phylogeny generated via RAxML and associated nonparametric bootstrap replicates f...
Recent advances in genomics have underscored the surprising ubiquity of DNA copy number variants (CN...
Maximum likelihood phylogeny generated using partitioned analysis in RAxML for 164 species
The CNest methods allow large scale CNV detection from very large WGS and WES datasets and generates...
Background Detection of copy number variation (CNV) in genes associated with disease is important in...
<p>The core genome phylogeny obtained by the maximum-likelihood method with x100 bootstrapping.</p
Copy number variation (CNV) is a type of genomic structural variation which has been associated with...
Analyses were based on full genomic sequences (i.e. including both variant and invariant sites)
Summary:Copy number variation is an important and abundant source of variation in the human genome, ...
Received on; revised on; accepted on Motivation: DNA copy number variants (CNV) are gains and losses...
Copy number variation (CNV) is a prevalent form of critical genetic variation that leads to an abnor...