Expert-led courses in genomics, proteomics, Python/R for biology, NGS analysis, and more. Join our research community today.
Every course, grouped by topic
Build a clear foundation in NGS analysis—from raw FASTQ reads and quality control to al...
Learn a practical CNV workflow for NGS data—from paired-end preparation and ExomeDepth ...
A focused introduction to phage genome assembly that takes you through the de novo anal...
Start using R and RStudio for bioinformatics through biological data, visualization, st...
Turn raw WES and targeted-panel reads into an analysis-ready VCF by processing FASTQ da...
Move from a raw VCF to prioritized candidates through annotation, evidence-based filter...
Turn complex WES findings into a clear molecular report, address secondary findings, an...
Master an integrated expression-analysis pathway covering bulk RNA-seq, single-cell RNA...
Build a complete bulk RNA-seq workflow—from experimental design and differential expres...
Progress from raw scRNA-seq reads to a cellular count matrix and Seurat-based clusterin...
A focused two-session course on discovering communication patterns between cell populat...
Connect the complete molecular workflow—from extraction and primer design to PCR, Sange...
Follow MLPA from sample preparation and laboratory execution to data analysis with Gene...
Insights, research, and updates from AD Bioinformatics
راهنمای جامع VarSage برای اولویت‌بندی و تفسیر واریانت‌های بیماری‌های نادر؛ آشنایی با تحلیل Singleton و Trio، غربالگری ناقل بودن، ورودی‌های WES/WGS، تط...
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دانلود منابع NGS بر اساس کاربرد: ژنوم مرجع، BQSR، VQSR، Mutect2 و پایگاه‌های ANNOVAR؛ همراه با نسخه ژنوم و لینک مستقیم.
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نحوه استفاده از نرم افزار 123VCF; ابزاری برای فیلتر فایل‌های VCF https://dl.adbioinformatics.net/PostVids/123VCF.mp4 دانلود مستقیم آخرین نسخه نرم‌افزا...
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