[HTML][HTML] Next-generation biology: sequencing and data analysis approaches for non-model organisms

RR da Fonseca, A Albrechtsen, GE Themudo… - Marine genomics, 2016 - Elsevier
As sequencing technologies become more affordable, it is now realistic to propose studying
the evolutionary history of virtually any organism on a genomic scale. However, when …

RNA sequencing data: hitchhiker's guide to expression analysis

K Van den Berge, KM Hembach… - Annual Review of …, 2019 - annualreviews.org
Gene expression is the fundamental level at which the results of various genetic and
regulatory programs are observable. The measurement of transcriptome-wide gene …

Transcriptome assembly from long-read RNA-seq alignments with StringTie2

S Kovaka, AV Zimin, GM Pertea, R Razaghi… - Genome biology, 2019 - Springer
RNA sequencing using the latest single-molecule sequencing instruments produces reads
that are thousands of nucleotides long. The ability to assemble these long reads can greatly …

A high quality Arabidopsis transcriptome for accurate transcript-level analysis of alternative splicing

R Zhang, CPG Calixto, Y Marquez… - Nucleic acids …, 2017 - academic.oup.com
Alternative splicing generates multiple transcript and protein isoforms from the same gene
and thus is important in gene expression regulation. To date, RNA-sequencing (RNA-seq) is …

Accurate assembly of transcripts through phase-preserving graph decomposition

M Shao, C Kingsford - Nature biotechnology, 2017 - nature.com
We introduce Scallop, an accurate reference-based transcript assembler that improves
reconstruction of multi-exon and lowly expressed transcripts. Scallop preserves long-range …

Leveraging transcript quantification for fast computation of alternative splicing profiles

GP Alamancos, A Pagès, JL Trincado, N Bellora… - Rna, 2015 - rnajournal.cshlp.org
Alternative splicing plays an essential role in many cellular processes and bears major
relevance in the understanding of multiple diseases, including cancer. High-throughput RNA …

Accurate genotyping across variant classes and lengths using variant graphs

JA Sibbesen, L Maretty… - Nature …, 2018 - nature.com
Genotype estimates from short-read sequencing data are typically based on the alignment of
reads to a linear reference, but reads originating from more complex variants (for example …

BaRTv2: a highly resolved barley reference transcriptome for accurate transcript‐specific RNA‐seq quantification

M Coulter, JC Entizne, W Guo, M Bayer… - The Plant …, 2022 - Wiley Online Library
Accurate characterisation of splice junctions (SJs) as well as transcription start and end sites
in reference transcriptomes allows precise quantification of transcripts from RNA‐seq data …

TransComb: genome-guided transcriptome assembly via combing junctions in splicing graphs

J Liu, T Yu, T Jiang, G Li - Genome biology, 2016 - Springer
Transcriptome assemblers aim to reconstruct full-length transcripts from RNA-seq data. We
present TransComb, a genome-guided assembler developed based on a junction graph …

Effects of transcriptional noise on estimates of gene and transcript expression in RNA sequencing experiments

A Varabyou, SL Salzberg, M Pertea - Genome research, 2021 - genome.cshlp.org
RNA sequencing is widely used to measure gene expression across a vast range of animal
and plant tissues and conditions. Most studies of computational methods for gene …