refphase: an R package for multi-region reference phasing of somatic copy-number alteration profiles from cancer sample
Abstract Background Somatic copy number alterations (CNAs) contribute to the clinically targetable a...
National audienceMPAgenomics, standing for multi-patients analysis of genomicmarkers, is an R-packag...
Archive contains a readme and an R source package for installation of MethylCIBERSORT. Validation an...
a) Refphase creates a minimum consistent segmentation across the single-sample segmentations input f...
Summary: The use of high-density SNP arrays for investigating copy number alterations in clinical tu...
A new procedure to align single nucleotide polymorphism (SNP) microarray signals for copy number ana...
Most computational methods that infer somatic copy number alterations (SCNAs) from bulk sequencing o...
Collections of genomic intervals are a common data type across many areas of computational biology. ...
deconstructSigs R package and README Takes sample information in the form of the fraction of mutati...
Background: Last generations of Single Nucleotide Polymorphism (SNP) arrays allow to study copy-numb...
AluScanCNV2 is an R package that integrates the cross-platform CNV detection and tumor prediction fu...
A new procedure to align single-nucleotide polymorphism (SNP) microarray signals for copy number ana...
The application of genome-wide approaches to the molecular characterization of cancer was investigat...
Motivation: Despite widespread prevalence of somatic structural variations (SVs) across most tumor t...
Submission contains R script for calculation of three signatures of Homologous Recombination Deficie...
Abstract Background Somatic copy number alterations (CNAs) contribute to the clinically targetable a...
National audienceMPAgenomics, standing for multi-patients analysis of genomicmarkers, is an R-packag...
Archive contains a readme and an R source package for installation of MethylCIBERSORT. Validation an...
a) Refphase creates a minimum consistent segmentation across the single-sample segmentations input f...
Summary: The use of high-density SNP arrays for investigating copy number alterations in clinical tu...
A new procedure to align single nucleotide polymorphism (SNP) microarray signals for copy number ana...
Most computational methods that infer somatic copy number alterations (SCNAs) from bulk sequencing o...
Collections of genomic intervals are a common data type across many areas of computational biology. ...
deconstructSigs R package and README Takes sample information in the form of the fraction of mutati...
Background: Last generations of Single Nucleotide Polymorphism (SNP) arrays allow to study copy-numb...
AluScanCNV2 is an R package that integrates the cross-platform CNV detection and tumor prediction fu...
A new procedure to align single-nucleotide polymorphism (SNP) microarray signals for copy number ana...
The application of genome-wide approaches to the molecular characterization of cancer was investigat...
Motivation: Despite widespread prevalence of somatic structural variations (SVs) across most tumor t...
Submission contains R script for calculation of three signatures of Homologous Recombination Deficie...
Abstract Background Somatic copy number alterations (CNAs) contribute to the clinically targetable a...
National audienceMPAgenomics, standing for multi-patients analysis of genomicmarkers, is an R-packag...
Archive contains a readme and an R source package for installation of MethylCIBERSORT. Validation an...
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