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ANNOVAR
Whole Genome Sequencing Identifies Novel Structural Variant in a Large Indian Family Affected with X - Linked Agammaglobulinemia
Exome Sequencing and Functional Validation in Zebrafish Identify
Genomic Approaches for Understanding the Genetics of Complex Disease
QTL Analysis Reveals Genomic Variants Linked to High-Temperature
A Comprehensive Database of Putative Human Microrna Target Site
Interleukin 10 Mutant Zebrafish Have an Enhanced Interferon
Comparison of Structural and Short Variants Detectedby Linked-Read
Variant Annotation
1 Mapping Challenging Mutations by Whole-Genome Sequencing Harold
Phase 3. Functional Variant Discovery
A Pipeline for Identifying Saccharomyces Cerevisiae Mutations
Gain-Of-Function Mutation of Microrna-140 in Human Skeletal Dysplasia
Improving Isobutanol Productivity Through Adaptive Laboratory Evolution in Saccharomyces Cerevisiae
Translating Cardiac and Cardiometabolic GWAS Using Zebrafish
Varaft: a Variant Annotation and Filtration System for Human Next
A Comprehensive Database of Putative Human Microrna Target Site
Genome-Wide Association Study Identifies Genetic Susceptibility Loci
An Integrated Platform for Cohort-Based Annotation
Top View
Caenorhabditis Elegans Is a Useful Model for Anthelmintic Discovery
Long-Read Sequencing Improves the Detection of Structural Variations Impacting Complex Non-Coding Elements of the Genome
Accurate Mutation Annotation and Functional Prediction Enhance the Applicability of -Omics Data in Precision Medicine
Genome-Wide Profiling of the C. Elegans Dsrnaome
Mutation of NEKL-4/NEK10 and TTLL Genes Opposes Loss of the CCPP-1 Deglutamylase and Prevents Neuronal Ciliary Degeneration
Rapid Online Variant Annotation and Natural-Language Filtering at Whole-Genome Scale Alex V
Intrastrain Genomic and Phenotypic Variability of the Commercial
Whole Genome Sequencing for The
Variant Annotation and Functional Prediction
Improving Dbnsfp
Using C. Elegans to Model Human TWIST Variants
Zebrafish Illumina Data Analysis Protocol
Whole-Exome Sequencing Identifies MST1R As a Genetic Susceptibility Gene in Nasopharyngeal Carcinoma
A Truncating Mutation in CEP55 Is the Likely Cause of MARCH, a Novel
Exome Sequencing Reveals Pathogenic Mutations in 91 Strains of Mice with Mendelian Disorders
Genomic Evolution of Saccharomyces Cerevisiae Under Chinese Rice Wine Fermentation
C. Elegans Development, Cell Biology, & Gene Expression Meeting 2012
Discriminating Somatic and Germline Mutations in Tumour DNA Samples Without Matching Normals