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Genetic insights into childhood-onset schizophrenia: The yield of clinical exome sequencing - ScienceDirect
Technologies for Genomic Medicine: The GMW, A Genetic Medical Workflow Engine The Team1: Phillips Owen, RENCI Research Software
GitHub - BCM-Lupskilab/HMZDelFinder: CNV calling algorithm for detection of homozygous and hemizygous deletions from whole exome sequencing data
20110114 Next Generation Sequencing Course
Analysis workflow to assess de novo genetic variants from human whole-exome sequencing - ScienceDirect
Whole-exome sequencing of individuals from an isolated population implicates rare risk variants in bipolar disorder | Translational Psychiatry
The Application of Validation and Proficiency Testing Concepts From Current Clinical Genetic Diagnostics For the Implementation of New Genetic Technologies. - ppt download
A survey of computational tools to analyze and interpret whole exome sequencing data - Document - Gale Academic OneFile
Whole Exome Sequencing - Are only protein-coding regions the best?
Exome-seq | Biostat Wiki
Copy-number: exomes vs genomes, proposing a better strategy - Enseqlopedia
Discovery and annotation of variants by exome analysis using NGS
JCI Insight - Whole-exome sequencing uncovers oxidoreductases DHTKD1 and OGDHL as linkers between mitochondrial dysfunction and eosinophilic esophagitis
Exome sequencing - Wikipedia
Whole genome sequencing - Wikipedia
Sequencing of 640,000 exomes identifies GPR75 variants associated with protection from obesity | Science
miRMut: Annotation of mutations in miRNA genes from human whole-exome or whole-genome sequencing - ScienceDirect
Exome Sequencing Identifies Genes and Gene Sets Contributing to Severe Childhood Obesity, Linking PHIP Variants to Repressed POMC Transcription - ScienceDirect