Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by J. Glessner
PennCNV: An Integrated Hidden Markov Model Designed for High-Resolution Copy Number Variation Detection in Whole-Genome SNP Genotyping Data
Genome Research
Genetics
Related publications
cnvHiTSeq: Integrative Models for High-Resolution Copy Number Variation Detection and Genotyping Using Population Sequencing Data
Genome Biology
An Evaluation of Copy Number Variation Detection Tools for Cancer Using Whole Exome Sequencing Data
BMC Bioinformatics
Biochemistry
Applied Mathematics
Computer Science Applications
Structural Biology
Molecular Biology
Genome-Wide Copy Number Variations Using SNP Genotyping in a Mixed Breed Swine Population
PLoS ONE
Multidisciplinary
A High Resolution Map of Segmental DNA Copy Number Variation in the Mouse Genome
PLoS Genetics
Evolution
Ecology
Genetics
Molecular Biology
Cancer Research
Systematics
Behavior
High-Resolution Copy Number Analysis of Paraffin-Embedded Archival Tissue Using SNP BeadArrays
Genome Research
Genetics
A Hidden Markov Model to Estimate Population Mixture and Allelic Copy-Numbers in Cancers Using Affymetrix SNP Arrays
BMC Bioinformatics
Biochemistry
Applied Mathematics
Computer Science Applications
Structural Biology
Molecular Biology
Genome-Wide Mapping of Copy Number Variations Using SNP Arrays
Transfusion Medicine and Hemotherapy
Allergy
Immunology
Hematology
High-Resolution Whole-Genome Haplotyping Using Limited Seed Data
Nature Methods
Biochemistry
Biotechnology
Cell Biology
Molecular Biology
Quantitative Assessment of Single-Cell Whole Genome Amplification Methods for Detecting Copy Number Variation Using Hippocampal Neurons
Scientific Reports
Multidisciplinary
