Training materials
Scientific topics: Sanger sequencing
and Keywords: Variant analysis
and Contributors: Erasmus Medical Center
1 material found
- Home
- Materials
Filters
Sort
-
-
Filter Clear filters
-
-
Scientific topic
- Sanger sequencing
- Chromosome walking1
- Clone verification1
- Comparative transcriptomics1
- DNA-Seq1
- DNase-Seq1
- High throughput sequencing1
- High-throughput sequencing1
- MicroRNA sequencing1
- NGS1
- NGS data analysis1
- Next gen sequencing1
- Next generation sequencing1
- Panels1
- Primer walking1
- RNA sequencing1
- RNA-Seq1
- RNA-Seq analysis1
- Sequencing1
- Small RNA sequencing1
- Small RNA-Seq1
- Small-Seq1
- Targeted next-generation sequencing panels1
- Transcriptome1
- Transcriptome profiling1
- Transcriptomics1
- Variant pattern analysis1
- WTSS1
- Whole transcriptome shotgun sequencing1
- miRNA-seq1
- Show N_FILTERS more
-
-
-
Content provider
- Glittr.org1
- Show N_FILTERS more
-
-
-
Difficulty level
- Not specified1
- Show N_FILTERS more
-
-
-
Contributor
- Erasmus Medical Center
- UC Davis Bioinformatics Core Training Page2
- Cloud-SPAN1
- Cornell University1
- Dipannita Ghosh1
- 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 Griffith Lab1
- The McDonnell Genome Institute1
- Waldron Lab at the CUNY SPH1
- liulab-dfci1
- rapidspeciation1
- Show N_FILTERS more
-
- Show archived materials
