RNA-seq has the potential to be used as a rapid diagnostic tool in genomic medicine

January 3, 2019 Leave a comment 2,868 Views

High-throughput next-generation sequencing technologies have led to a rapid increase in the number of sequence variants identified in clinical practice via diagnostic genetic tests. Current bioinformatic analysis pipelines fail to take adequate account...

RNA-Seq Blog Transcriptome Research & Industry News

Tag Archives: Sequence variants

RNA-seq has the potential to be used as a rapid diagnostic tool in genomic medicine

Normalized counts performs better than TPM, FPKM for hierarchical clustering of replicate RNA-Seq samples

COVseq – Low-cost method for finding new coronavirus variants

Labcorp adopts Molecular Loop SARS-CoV-2 targeted RNA sequencing panel for large-scale viral surveillance

Integration of millions of transcriptomes using batch-aware triplet neural networks

Profiling gene expression in plant embryos one nucleus at a time

Single-cell CUT&Tag to identify cell states in normal and disease tissue

The triumphs and limitations of computational methods for scRNA-seq