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Process / pipelineBioinformatics / omics

Uchambuzi wa Tofauti ya Idadi ya Nakala kwa Kutumia Mtandao

Uchambuzi wa tofauti ya idadi ya nakala (CNV) kwa kutumia mtandao huunganisha data ya CNV ya jenomu nzima na mitandao ya mwingiliano wa kibiolojia — kama vile mwingiliano wa protini-protini (PPI) au mitandao ya njia — ili kutambua maeneo yenye utendaji thabiti, jeni tegemezi, na subnetworks zilizobadilika ambazo utambuzi wa CNV pekee usingeweza kuziona. Kwa kusambaza ishara za CNV kupitia grafu ya mtandao, njia hii hufichua usawa wa kipimo cha jenomu ulioratibiwa unaoelekea kwenye kazi za kawaida za kibiolojia, na kuifanya kuwa na nguvu hasa katika jenomiki ya saratani na tafiti za magonjwa adimu.

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Vyanzo

  1. Vandin, F., Upfal, E., & Raphael, B. J. (2012). De novo discovery of mutated driver pathways in cancer. Genome Research, 22(2), 375–385. DOI: 10.1101/gr.120477.111
  2. Leiserson, M. D. M., Vandin, F., Wu, H.-T., Dobson, J. R., Eldridge, J. V., Thomas, J. L., Papoutsaki, A., Kim, Y., Niu, B., McLellan, M., Lawrence, M. S., Gonzalez-Perez, A., Tamborero, D., Cheng, Y., Ryslik, G. A., Lopez-Bigas, N., Getz, G., Ding, L., & Raphael, B. J. (2015). Pan-cancer network analysis identifies combinations of rare somatic mutations across pathways and protein complexes. Nature Genetics, 47(2), 106–114. DOI: 10.1038/ng.3168

Jinsi ya kunukuu ukurasa huu

ScholarGate. (2026, June 3). Network-Based Copy Number Variation Analysis. ScholarGate. https://scholargate.app/sw/bioinformatics/network-based-copy-number-variation-analysis

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ScholarGateNetwork-based copy number variation analysis (Network-Based Copy Number Variation Analysis). Imepatikana 2026-06-15 kutoka https://scholargate.app/sw/bioinformatics/network-based-copy-number-variation-analysis · Seti ya data: https://doi.org/10.5281/zenodo.20539026