The following pages link to GATK (Q23953):
Displayed 16 items.
- An overview of multiple sequence alignments and cloud computing in bioinformatics (Q470592) (← links)
- Detecting mutations in mixed sample sequencing data using empirical Bayes (Q714364) (← links)
- A Bayesian feature allocation model for tumor heterogeneity (Q746649) (← links)
- Variance in estimated pairwise genetic distance under high versus low coverage sequencing: the contribution of linkage disequilibrium (Q1746104) (← links)
- TreeClone: reconstruction of tumor subclone phylogeny based on mutation pairs using next generation sequencing data (Q2318663) (← links)
- An external-memory algorithm for string graph construction (Q2362353) (← links)
- An empirical Bayes testing procedure for detecting variants in analysis of next generation sequencing data (Q2441858) (← links)
- Estimating Latent Cell Subpopulations with Bayesian Feature Allocation Models (Q2800190) (← links)
- Empirical Bayes scan statistics for detecting clusters of disease risk variants in genetic studies (Q2809542) (← links)
- Error Correction in Methylation Profiling From NGS Bisulfite Protocols (Q3305529) (← links)
- CUSHAW Suite: Parallel and Efficient Algorithms for NGS Read Alignment (Q3305533) (← links)
- Efficiently Inferring the Demographic History of Many Populations With Allele Count Data (Q5120682) (← links)
- Computational Genomics with R (Q5151092) (← links)
- (Q5212398) (← links)
- A statistical method for detecting differentially expressed SNVs based on next‐generation RNA‐seq data (Q5347401) (← links)
- (Q5371992) (← links)