GATK

swMATH12019MaRDI QIDQ23953FDOQ23953

Author name not available (Why is that?)

Cited In (16)

• Empirical Bayes scan statistics for detecting clusters of disease risk variants in genetic studies
• Error correction in methylation profiling from NGS bisulfite protocols
• TreeClone: reconstruction of tumor subclone phylogeny based on mutation pairs using next generation sequencing data
• A statistical method for detecting differentially expressed SNVs based on next-generation RNA-seq data
• Detecting mutations in mixed sample sequencing data using empirical Bayes
• Estimating Latent Cell Subpopulations with Bayesian Feature Allocation Models
• An empirical Bayes testing procedure for detecting variants in analysis of next generation sequencing data
• Variance in estimated pairwise genetic distance under high versus low coverage sequencing: the contribution of linkage disequilibrium
• An external-memory algorithm for string graph construction
• A Bayesian feature allocation model for tumor heterogeneity
• An overview of multiple sequence alignments and cloud computing in bioinformatics
• Computational exome and genome analysis
• Analysis of expression profile and gene variation via development of methods for next generation sequencing data
• Computational genomics with R. With the assistance of Verdan Franke, Bora Uyar and Jonathan Ronen
• CUSHAW suite: parallel and efficient algorithms for NGS read alignment
• Efficiently inferring the demographic history of many populations with allele count data

This page was built for software: GATK