Training materials
Keywords: Variant analysis
and Scientific topics: NGS data analysis
and Contributors: The Griffith Lab
1 material found
- Home
- Materials
Filter
Sort
-
-
Filter Clear filters
-
-
Scientific topic
- NGS data analysis
- CWL1
- Chromosome walking1
- Clone verification1
- Common Workflow Language1
- CommonWL1
- Comparative transcriptomics1
- DNA-Seq1
- DNase-Seq1
- Exomes1
- Genome annotation1
- Genomes1
- Genomics1
- High throughput sequencing1
- High-throughput sequencing1
- NGS1
- Next gen sequencing1
- Next generation sequencing1
- Panels1
- Personal genomics1
- Primer walking1
- Sanger sequencing1
- Sequencing1
- Synthetic genomics1
- Targeted next-generation sequencing panels1
- Transcriptome1
- Transcriptomics1
- Variant pattern analysis1
- Viral genomics1
- Whole genomes1
- Show N_FILTERS more
-
-
-
Content provider
- Glittr.org1
- Show N_FILTERS more
-
-
-
Difficulty level
- Not specified1
- Show N_FILTERS more
-
-
-
Licence
- MIT License1
- Show N_FILTERS more
-
-
-
Contributor
- The Griffith Lab
- UC Davis Bioinformatics Core Training Page2
- Cloud-SPAN1
- Cornell University1
- Dipannita Ghosh1
- Erasmus Medical Center1
- Fred Hutch Data Science Lab1
- Galaxy Project1
- Institut Français de Bioinformatique (IFB)1
- Jio Institute1
- NBIS - National Bioinformatics Infrastructure Sweden1
- Nina Overgaard Therkildsen1
- SIB Swiss Institute of Bioinformatics1
- St. Jude Children's Research Hospital1
- Teaching materials at the Harvard Chan Bioinformatics Core1
- The McDonnell Genome Institute1
- Waldron Lab at the CUNY SPH1
- liulab-dfci1
- rapidspeciation1
- Show N_FILTERS more
-
- Show disabled materials
- Show archived materials
