 | | Working with RNA-seq data (bam) | | | Question | | | Can I work with RNA-seq data? | | Answer | | Yes you can analyze RNA-seq data already with the base module. If you also have the NGS Module you can analyze your RNA-seq data both by doing statistical filtering on expression levels and by doing filtering on genomic entities and inspecting results in the Genome browser. | | Related articles | - How to import data (RNA-seq, Illumina, Olink, Affymetrix, 10x, Agilent, Wizard, tab separated, csv, txt, bam)
- Low expression levels RNA-seq data filtering
- BAM file sort order
- Biosulfite sequencing
- ChIP-seq and ATAC-seq
- DESeq2
- How are counts counted when importing bam files?
- How does Qlucore calculate the length of the gene to do the normalization?
- How to import 10X single cell data
- Normalization of imported RNA-seq data
- Normalize RNA-seq data in R
- RNAseq and array technologies
- RNA-seq normalization for BAM files
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