विधियों की तुलना करें
चुनी हुई विधियों की आमने-सामने समीक्षा करें; भिन्नता वाली पंक्तियाँ रेखांकित हैं।
| CRISPR स्क्रीन विश्लेषण× | डी नोवो ट्रांसक्रिप्टोम असेंबली (De Novo Transcriptome Assembly)× | |
|---|---|---|
| क्षेत्र | जैव सूचना विज्ञान | जैव सूचना विज्ञान |
| परिवार | Process / pipeline | Process / pipeline |
| उद्भव वर्ष≠ | 2013 | 2011 |
| प्रवर्तक≠ | Feng Zhang | Aviv Regev |
| प्रकार≠ | High-throughput genetic screen pipeline | Sequence assembly pipeline |
| मौलिक स्रोत≠ | 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 ↗ | Grabherr, 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 ↗ |
| उपनाम≠ | CRISPR pooled screen, genetic screen analysis | transcriptome assembly, de novo assembly, RNA-Seq assembly |
| संबंधित | 3 | 3 |
| सारांश≠ | 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. | De 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. |
| ScholarGateडेटासेट ↗ |
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