RiboLace, a novel method using a unique puromycin derivative molecule, specifically captures actively translating ribosomes, enabling detailed analysis of genome-wide translation activity at single-nucleotide resolution.
Ribosome profiling identifies translating RNA, but sequencing struggles with abundant rRNA. Removing rRNA boosts relevant reads (80-90%). Different methods have advantages and limitatations. Choosing the best method depends on your experiment.
Nano-tRNAseq, a new method using nanopores, allows for simultaneous quantification of tRNA abundance and modifications in a single experiment. This overcomes limitations of previous methods and reveals details of tRNA populations in yeast under stress.
Ribo-Zero rRNA depletion kit discontinued. New alternatives unsuited for ribosome profiling. Consider traditional biotinylated oligos for accurate translation analysis.
SMN protein, linked to spinal muscular atrophy (SMA), steers ribosomes on specific mRNAs affecting translation of key neuronal proteins. Loss of SMN disrupts this process, contributing to SMA.
New R package (expressyouRcell) simplifies visualizing complex gene expression data across time, space, and single cells. It uses dynamic cell pictographs for clear communication of results, improving on traditional quantitative methods.
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