Somatic structural variants are an important contributor to cancer development and evolution. Accurate detection of these complex variants from whole genome sequencing data is influenced by a multitude of parameters. However, there are currently no tools for guiding study design nor are there applications that could predict the performance of somatic structural variant detection. To address this gap, we developed Shiny-SoSV, a user-friendly web-based calculator for determining the impact of common variables on the sensitivity, precision and F1 score of somatic structural variant detection, including choice of variant detection tool, sequencing depth of coverage, variant allele fraction, and variant breakpoint resolution. Using simulation st...
[eng] The identification and analysis of genomic variation across individuals has been central in bi...
Structural variants (SVs) are the hidden architecture of the human genome, and are critical for us t...
Cancer, which affects hundreds of thousands of people worldwide every year and costs billions in tre...
BackgroundThe phenotypes of cancer cells are driven in part by somatic structural variants. Structur...
BackgroundThe phenotypes of cancer cells are driven in part by somatic structural variants. Structur...
Abstract Background The phenotypes of cancer cells ar...
Abstract Background The phenotypes of cancer cells ar...
BackgroundThe phenotypes of cancer cells are driven in part by somatic structural variants. Structur...
Abstract Background The phenotypes of cancer cells are driven in part by somatic structural variants...
SomaticSeq is an accurate somatic mutation detection pipeline implementing a stochastic boosting alg...
Structural variations (SVs) are genomic variants that typically impact more than 50 nucleotides in l...
Motivation: Despite widespread prevalence of somatic structural variations (SVs) across most tumor t...
The identification and analysis of genomic variation across individuals has been central in biology,...
Motivation: Despite widespread prevalence of somatic structural variations (SVs) across most tumor t...
Motivation: Despite widespread prevalence of somatic structural variations (SVs) across most tumor t...
[eng] The identification and analysis of genomic variation across individuals has been central in bi...
Structural variants (SVs) are the hidden architecture of the human genome, and are critical for us t...
Cancer, which affects hundreds of thousands of people worldwide every year and costs billions in tre...
BackgroundThe phenotypes of cancer cells are driven in part by somatic structural variants. Structur...
BackgroundThe phenotypes of cancer cells are driven in part by somatic structural variants. Structur...
Abstract Background The phenotypes of cancer cells ar...
Abstract Background The phenotypes of cancer cells ar...
BackgroundThe phenotypes of cancer cells are driven in part by somatic structural variants. Structur...
Abstract Background The phenotypes of cancer cells are driven in part by somatic structural variants...
SomaticSeq is an accurate somatic mutation detection pipeline implementing a stochastic boosting alg...
Structural variations (SVs) are genomic variants that typically impact more than 50 nucleotides in l...
Motivation: Despite widespread prevalence of somatic structural variations (SVs) across most tumor t...
The identification and analysis of genomic variation across individuals has been central in biology,...
Motivation: Despite widespread prevalence of somatic structural variations (SVs) across most tumor t...
Motivation: Despite widespread prevalence of somatic structural variations (SVs) across most tumor t...
[eng] The identification and analysis of genomic variation across individuals has been central in bi...
Structural variants (SVs) are the hidden architecture of the human genome, and are critical for us t...
Cancer, which affects hundreds of thousands of people worldwide every year and costs billions in tre...