17 results on '"Salerno, William J."'
Search Results
2. Open-source mapping and variant calling for large-scale NGS data from original base-quality scores
3. Sparse Project VCF: efficient encoding of population genotype matrices
4. Parliament2: Accurate structural variant calling at scale
5. SVCollector: Optimized sample selection for cost-efficient long-read population sequencing
6. Quality control and integration of genotypes from two calling pipelines for whole genome sequence data in the Alzheimer's disease sequencing project
7. VCPA: genomic variant calling pipeline and data management tool for Alzheimer’s Disease Sequencing Project
8. Sparse Project VCF: efficient encoding of population genotype matrices
9. VCPA: genomic variant calling pipeline and data management tool for Alzheimer’s Disease Sequencing Project
10. O3‐06‐01: WHOLE EXOME SEQUENCING STUDY IDENTIFIES RARE COPY NUMBER VARIATIONS FOR LATE‐ONSET ALZHEIMER'S DISEASE: THE ALZHEIMER'S DISEASE SEQUENCING PROJECT CASE‐CONTROL ANALYSIS
11. P4‐044: THE GCAD CLOUD‐BASED WORKFLOW FOR PROCESSING WHOLE EXOME AND WHOLE GENOME DATA FROM THE ALZHEIMER'S DISEASE SEQUENCING PROJECT
12. GLnexus: joint variant calling for large cohort sequencing
13. SVCollector: Optimized sample selection for validating and long-read resequencing of structural variants
14. SVachra: a tool to identify genomic structural variation in mate pair sequencing data containing inward and outward facing reads
15. Assessing structural variation in a personal genome—towards a human reference diploid genome
16. PBHoney: identifying genomic variants via long-read discordance and interrupted mapping
17. Solution Structure of a CUE-Ubiquitin Complex Reveals a Conserved Mode of Ubiquitin Binding
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.