[HTML][HTML] Full-length transcript sequencing of human and mouse cerebral cortex identifies widespread isoform diversity and alternative splicing

SK Leung, AR Jeffries, I Castanho, BT Jordan, K Moore… - Cell reports, 2021 - cell.com
Alternative splicing is a post-transcriptional regulatory mechanism producing distinct mRNA
molecules from a single pre-mRNA with a prominent role in the development and function of …

Exploring the relationship between fusion genes and MicroRNAs in cancer

S Panicker, G Chengizkhan, R Gor, I Ramachandran… - Cells, 2023 - mdpi.com
Fusion genes are key cancer driver genes that can be used as potential drug targets in
precision therapies, and they can also serve as accurate diagnostic and prognostic …

Sequencing strategies for fusion gene detection

EE Heyer, J Blackburn - Bioessays, 2020 - Wiley Online Library
Fusion genes formed by chromosomal rearrangements are common drivers of cancer.
Recent innovations in the field of next‐generation sequencing (NGS) have seen a dynamic …

22q11. 2 low copy repeats expanded in the human lineage

L Vervoort, N Dierckxsens, Z Pereboom… - Frontiers in …, 2021 - frontiersin.org
Segmental duplications or low copy repeats (LCRs) constitute duplicated regions
interspersed in the human genome, currently neglected in standard analyses due to their …

Low copy repeats in the genome: From neglected to respected

L Vervoort, JR Vermeesch - Exploration of Medicine, 2023 - explorationpub.com
DNA paralogs that have a length of at least 1 kilobase (kb) and are duplicated with a
sequence identity of over 90% are classified as low copy repeats (LCRs) or segmental …

Bursts of novel composite gene families at major nodes in animal evolution

PO Mulhair, RJ Moran, JS Pathmanathan, D Sussfeld… - bioRxiv, 2023 - biorxiv.org
A molecular level perspective on how novel phenotypes evolve is contingent on our
understanding of how genomes evolve through time, and of particular interest is how novel …

Full-length transcript sequencing of human and mouse identifies widespread isoform diversity and alternative splicing in the cerebral cortex

AR Jeffries, SK Leung, I Castanho, K Moore, JP Davies… - bioRxiv, 2020 - biorxiv.org
Alternative splicing is a post-transcriptional regulatory mechanism producing multiple
distinct mRNA molecules from a single pre-mRNA. Alternative splicing has a prominent role …

An atlas of expressed transcripts in the prenatal and postnatal human cortex

R Bamford, SK Leung, VK Chundru, AR Jeffries… - bioRxiv, 2024 - biorxiv.org
Alternative splicing is a post-transcriptional mechanism that increases the diversity of
expressed transcripts and plays an important role in regulating gene expression in the …

Eukaryote genes are more likely than prokaryote genes to be composites

Y Ou, JO McInerney - Genes, 2019 - mdpi.com
The formation of new genes by combining parts of existing genes is an important
evolutionary process. Remodelled genes, which we call composites, have been investigated …

[图书][B] Genomic characterisation of Alzheimer's disease risk genes using long-read sequencing

SK Leung - 2022 - search.proquest.com
Alzheimer's disease (AD) is a devastating neurodegenerative disorder characterised by
progressive intracellular accumulation of hyperphosphorylated tau and extracellular …