A webtool for the clinical interpretation of CNVs in rare disease patients
#博客#A fully-functional & foolproof Laravel Blog + Publishing Platform built on https://github.com/cnvs/canvas
Package for easy and fast prediction and interpretation of the clinical impact of Copy Number Variants (CNVs)
Automated Validation of CNV calls from SNPs array
This is the github repository for the Eichler lab Amazon Web Services (AWS) pipelines
Codes for genome sequencing class being taught by Tychele N. Turner, Ph.D.
Codes for exome sequencing class being taught by Tychele N. Turner, Ph.D.
Supporting material for H3Africa Structural and Copy Number Variant paper: summary data and scripts
CNVs-study-from-SNPs-arrays describes a workflow to detect and analyze CNVs out of large scale microarray-based genotype data.