Browse Articles | Genetics in Medicine
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Topics – GATK
Genome Analysis Toolkit Variant Discovery in High-Throughput Sequencing Data Need Help? Search our documentation Community Forum Hi, How can we help? Developed in the Data Sciences Platform at the Broad Institute, the toolkit offers a wide variety of tools with a primary focus on variant discovery and genotyping. Its powerful processing engine and high-performance computing features make it capabl
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GitHub - pbnjay/lollipops: This is the development fork - Stable code has been moved to ==>
Improving genetic diagnosis in Mendelian disease with transcriptome sequencing – a walk through
FermiKit: assembly-based variant calling for Illumina resequencing data
Home - QIAGEN Digital Insights
A Guide to the Exome Aggregation Consortium (ExAC) Data Set
GATK
Variant Notation: In simplicity we find complexity - The Golden Helix Blog
GitHub - konradjk/loftee
AAAS
Exome Sequencing Links Corticospinal Motor Neuron Disease to Common Neurodegenerative Disorders
Gerstein Lab Tools
GitHub - bcbio/bcbio-nextgen: Validated, scalable, community developed variant calling, RNA-seq and small RNA analysis
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FoldX tools in YASARA - FoldX plugin for YASARA
FoldX plugin for YASARA - FoldX plugin for YASARA
Training exercises - FoldX plugin for YASARA
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