Cancer is a complex and deadly disease that is caused by genetic lesions in somatic cells. Further research in computational methodology for detecting and characterizing somatic mutations is necessary in order to understand the comprehensive systems level model of the roles of those lesions in cancer development. In the first project, I trained a list of supervised machine learning classifiers that classify false positive versus true positive somatic single nucleotide variants (SNVs). I was able to show an improvement of somatic SNV detection on the data set over the reported classifier. In the second project, we developed PhyloSub model that uses a nonparametric Bayesian prior over a set of trees to cluster SNVs, and infer the subclonal ph...
BackgroundNext-generation sequencing (NGS) panels for mature B-cell neoplasms (MBNs) are widely appl...
Somatic mutations promote the transformation of normal cells to cancer. Accurate identification of s...
A recent study showed that somatic mutations of well-known cancer driver genes, found in circulating...
Cancer is a complex and deadly disease that is caused by genetic lesions in somatic cells. Further r...
Motivation: The study of cancer genomes now routinely involves using next-generation sequencing tech...
Abstract Background High-throughput sequencing allows...
Copyright © 2015 Yukun Chen et al. This is an open access article distributed under the Creative Com...
International audienceSince 2017, we have used IonTorrent NGS platform in our hospital to diagnose a...
Deep learning could be applied to the challenge of somatic variant calling in cancer by making use o...
BackgroundNext-generation sequencing (NGS) panels for mature B-cell neoplasms (MBNs) are widely appl...
Somatic single nucleotide variants (SNVs) are mutations resulting from the substitution of a single ...
SomaticSeq is an accurate somatic mutation detection pipeline implementing a stochastic boosting alg...
BackgroundNext-generation sequencing (NGS) panels for mature B-cell neoplasms (MBNs) are widely appl...
In 2018, an estimated 1,762,450 new cases of cancer will be diagnosed in the United States and 606,8...
International audienceAbstract Background Next generation sequencing instruments are providing new o...
BackgroundNext-generation sequencing (NGS) panels for mature B-cell neoplasms (MBNs) are widely appl...
Somatic mutations promote the transformation of normal cells to cancer. Accurate identification of s...
A recent study showed that somatic mutations of well-known cancer driver genes, found in circulating...
Cancer is a complex and deadly disease that is caused by genetic lesions in somatic cells. Further r...
Motivation: The study of cancer genomes now routinely involves using next-generation sequencing tech...
Abstract Background High-throughput sequencing allows...
Copyright © 2015 Yukun Chen et al. This is an open access article distributed under the Creative Com...
International audienceSince 2017, we have used IonTorrent NGS platform in our hospital to diagnose a...
Deep learning could be applied to the challenge of somatic variant calling in cancer by making use o...
BackgroundNext-generation sequencing (NGS) panels for mature B-cell neoplasms (MBNs) are widely appl...
Somatic single nucleotide variants (SNVs) are mutations resulting from the substitution of a single ...
SomaticSeq is an accurate somatic mutation detection pipeline implementing a stochastic boosting alg...
BackgroundNext-generation sequencing (NGS) panels for mature B-cell neoplasms (MBNs) are widely appl...
In 2018, an estimated 1,762,450 new cases of cancer will be diagnosed in the United States and 606,8...
International audienceAbstract Background Next generation sequencing instruments are providing new o...
BackgroundNext-generation sequencing (NGS) panels for mature B-cell neoplasms (MBNs) are widely appl...
Somatic mutations promote the transformation of normal cells to cancer. Accurate identification of s...
A recent study showed that somatic mutations of well-known cancer driver genes, found in circulating...