Home page | Genome Biology
Home page | Genome Biology
Structural variant calling: the long and the short of it - UCL Discovery
Opportunities and challenges in long-read sequencing data analysis | Genome Biology | Full Text
Genome Biology
Strand-specific RNA sequencing reveals extensive regulated long antisense transcripts that are conserved across yeast species | Genome Biology | Full Text
Sequence context affects the rate of short insertions and deletions in flies and primates | Genome Biology | Full Text
Articles | Genome Biology
PDF) Paragraph: A graph-based structural variant genotyper for short-read sequence data
Genome Project Under Way, at Last | Science
PDF) Consequences and opportunities arising due to sparser single-cell RNA-seq datasets
Giotto: a toolbox for integrative analysis and visualization of spatial expression data | Genome Biology | Full Text
A high-resolution single-molecule sequencing-based Arabidopsis transcriptome using novel methods of Iso-seq analysis | Genome Biology | Full Text
PDF) ALLPATHS 2: Small genomes assembled accurately and with high continuity from short paired reads
PDF) Tsai IJ, Otto TD, Berriman M.. Improving draft assemblies by iterative mapping and assembly of short reads to eliminate gaps. Genome Biol 11: R41
A large-sample crisis or not? Exaggerated false positives by popular differential expression methods on human population RNA-seq samples | by Jingyi Jessica Li | Towards Data Science
Structural variant calling: the long and the short of it | Genome Biology | Full Text
Sequence context affects the rate of short insertions and deletions in flies and primates | Genome Biology | Full Text
Current status and applications of genome-scale metabolic models | Genome Biology | Full Text
Opportunities and challenges in long-read sequencing data analysis | Genome Biology | Full Text
EMIRGE: reconstruction of full-length ribosomal genes from microbial community short read sequencing data | Genome Biology | Full Text
Best practices for the interpretation and reporting of clinical whole genome sequencing | npj Genomic Medicine
