Browse Articles | Genetics in Medicine
Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.
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
リリース、障害情報などのサービスのお知らせ
最新の人気エントリーの配信
j次のブックマーク
k前のブックマーク
lあとで読む
eコメント一覧を開く
oページを開く
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
https://bioinformatics.oxfordjournals.org/content/early/2015/07/25/bioinformatics.btv440.abstract
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
Redirecting...
PON-P2
Error - Cookies Turned Off
FoldX tools in YASARA - FoldX plugin for YASARA
FoldX plugin for YASARA - FoldX plugin for YASARA
Training exercises - FoldX plugin for YASARA