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SNP array
Genome-Wide Human SNP Array 6.0
An Integrated Map of Genetic Variation from 1,092 Human Genomes
Chromosome SNP Microarray a New High-Density Allele-Specific Diagnostic Platform
Identity-By-Descent Detection Across 487,409 British Samples Reveals Fine Scale Population Structure and Ultra-Rare Variant Asso
Regions of Homozygosity Identified by SNP Microarray Analysis Aid in The
Genetic Profiles of 103,106 Individuals in the Taiwan Biobank Provide Insights Into the Health and History of Han Chinese
SNP Ascertainment Bias in Population Genetic Analyses: Why It Is Important, and How to Correct It Recently in Press
Mutagenesys: Estimating Individual Disease Susceptibility Based On
Pharmacogenomics and Personalized Medicine: the Plunge Into Next-Generation Sequencing Mia Wadelius1* and Ana AlRevic2
Human Identification by Genotyping Single Nucleotide Polymorphisms (Snps) Using an APEX Microarray
Genome-Wide Human SNP Array 5.0. Data Sheet
Europe PMC Funders Group Author Manuscript Nat Genet
Impact of SNP Microarray Analysis of Compromised DNA on Kinship Classification
Basic Principles and Laboratory Analysis of Genetic Variation Jesus Gonzalez-Bosquet and Stephen J
Statistical Analysis of Single Nucleotide Polymorphism Microarrays in Cancer Studies Pierre Neuvial, Henrik Bengtsson, Terence Speed
Integrating Sequence and Array Data to Create an Improved 1000 Genomes Project Haplotype Reference Panel
SNP-Array Lesions in Core Binding Factor Acute Myeloid Leukemia
The 1000 Genomes Project
Top View
Molecular Genetic Testing and the Future of Clinical Genomics
The Cytoscan HD Array in the Diagnosis of Neurodevelopmental Disorders
A Fast and Accurate SNP Detection Algorithm for Next-Generation Sequencing Data
Genome Organization and Pharmacogenomics
A 62K Genic-SNP Chip Array for Genetic Studies and Breeding Applications in Pigeonpea (Cajanus Cajan L
Personal Genomics
High-Density Single Nucleotide Polymorphism Array Analysis and ASXL1 Gene Mutation Screening in Chronic Myeloid Leukemia During Disease Progression
Axiom® Genome-Wide EUR 1 Array
Genetic Data
Acquired Copy Number Alterations in Adult Acute Myeloid Leukemia Genomes
The 1000 Genomes Project Datasets
CLOSING CASES with a SINGLE SNP ARRAY: INTEGRATED GENETIC GENEALOGY, DNA PHENOTYPING, and KINSHIP ANALYSES Ellen Greytak, Cece Moore Parabon Nanolabs, Inc
Application of Genome-Wide Single-Nucleotide Polymorphism Arrays to Understanding Dog Disease and Evolution
Cytogenetics Into Cytogenomics: SNP Arrays Expand the Screening Capabilities of Genetics Laboratories Contributed by Laura K
Pharmacogenomics: JMP® Right In!
Comparison of Array Platforms for Detection of Copy-Number Variation and Copy-Neutral Abnormalities
Affymetrix® Genome-Wide Human SNP Nsp/Sty Assay 5.0
Development and Validation of a Combined Species SNP Array for the European Seabass (Dicentrarchus Labrax) and Gilthead Seabream (Sparus Aurata)
Pharmacogenetics Pharmacogenetics of Severe Adverse Drug Reaction
NHANES Genetics Program Update
Using Whole-Genome Sequencing Data to Derive the Homologous Recombination Deficiency Scores
Cytogenetic Analysis by High-Resolution SNP Array
The Korea Biobank Array: Design and Identification of Coding Variants
Pharmacogenomics: Accessing Important Alleles by Imputation from Commercial Genome-Wide SNP Arrays
UK Biobank Axiom Array UK Biobank Axiom Array Advancing Human Health Studies with Powerful Genotyping Technology
The Rewards and Challenges of Array-Based Karyotyping for Clinical Oncology Applications
Population Assignment from Cancer Genome Profiling Data
Genomic Alterations in High-Risk Chronic Lymphocytic Leukemia Frequently Affect Cell Cycle Key Regulators and NOTCH1-Regulated Transcription
SNP Array Pre-Test Counseling Information
Data Sheet,Axiom Genome-Wide Pan-African Array
Technologies for Pharmacogenomics: a Review
Development and Evaluation of the Ancestry Informative Marker Panel of the VISAGE Basic Tool
The Power of High-Resolution SNP Arrays for Detecting Inherited Chromosomal Anomalies
Comprehensive Performance Comparison of High-Resolution Array Platforms for Genome-Wide Copy Number Variation (CNV) Analysis in Humans Rajini R
Array Differences in Genomic Coverage and Data Quality Impact GWAS Success David Delano, Michael Eberle, Luana Galver, and Carsten Rosenow*
Whole Genome SNP Arrays As a Potential Diagnostic Tool for the Detection of Characteristic Chromosomal Aberrations in Renal Epithelial Tumors
1 Technical Design Document for a SNP Array That Is Optimized For
Agilent's Sureprint G3 CGH+SNP Microarray Platform
Removing the SNP with the Lowest Combined Mtdna-CN GWAS and TFAM Eqtl P-Value
High Density SNP Microarray Also Known As: Copy Number + SNP Array
Recent Large-Scale Genotyping and Phenotyping of Plant Genetic Resources of Vegetatively Propagated Crops
The Use of ``Genotyping-By-Sequencing
Genotype Fingerprints Enable Fast and Private Comparison of Genetic Testing Results for Research and Direct-To-Consumer Applications
SNP Array Interpretation Guide