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Prohlédněte si vybrané metody vedle sebe; řádky, které se liší, jsou zvýrazněny.

De novo sestavení transkriptomu×Analýza CRISPR screeningů×
OborBioinformatikaBioinformatika
RodinaProcess / pipelineProcess / pipeline
Rok vzniku20112013
TvůrceAviv RegevFeng Zhang
TypSequence assembly pipelineHigh-throughput genetic screen pipeline
Původní zdrojGrabherr, M. G., Haas, B. J., Yassour, M., Levin, J. Z., Thompson, D. A., Amit, I., ... & Regev, A. (2011). Full-length transcriptome assembly from RNA-Seq data without a reference genome. Nature Biotechnology, 29(7), 644-652. DOI ↗Shalem, O., Sanjana, N. E., Hartenian, E., Shi, X., Scott, D. A., Mikkelsen, T. S., ... & Zhang, F. (2014). Genome-scale CRISPR-Cas9 knockout screening in human cells. Science, 343(6166), 84-87. DOI ↗
Další názvytranscriptome assembly, de novo assembly, RNA-Seq assemblyCRISPR pooled screen, genetic screen analysis
Příbuzné33
ShrnutíDe novo transcriptome assembly reconstructs full-length messenger RNA sequences directly from sequencing reads without requiring a reference genome. Pioneered by Regev, Haas, and colleagues, this pipeline enables transcript discovery in non-model organisms and detection of novel isoforms, fusion genes, and splice variants.CRISPR screen analysis processes data from pooled genetic screens using CRISPR-Cas9 to identify genes required for cell growth, survival, or phenotype in specific conditions. Developed by Zhang, Sanjana, and others, this computational pipeline transforms sequencing readouts of guide RNA abundances into ranked lists of functional genes.
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ScholarGatePorovnat metody: De Novo Transcriptome Assembly · CRISPR Screen Analysis. Získáno 2026-06-18 z https://scholargate.app/cs/compare