ScholarGate
دستیار

مقایسهٔ روش‌ها

روش‌های انتخابی خود را کنار هم مرور کنید؛ ردیف‌های متفاوت برجسته شده‌اند.

تحلیل فیلوژنتیک تک‌سلولی×تحلیل تغییرات تعداد کپی×
حوزهزیست‌اطلاعاتیزیست‌اطلاعاتی
خانوادهProcess / pipelineProcess / pipeline
سال پیدایش2014-2020 (rapid development period)1998–2006
پدیدآورMultiple groups; foundational tools: Trapnell et al. (Monocle, 2014), Jones et al. (Cassiopeia, 2020)Pinkel et al. (array CGH); Redon et al. (genome-wide CNV map)
نوعComputational phylogenetic inference pipelineGenomic structural variant detection pipeline
منبع بنیادینJones, M. G., Khodaverdian, A., Quinn, J. J., Chan, M. M., Hussmann, J. A., Wang, R., Xu, C., Weissman, J. S., & Yosef, N. (2020). Inference of single-cell phylogenies from lineage tracing data using Cassiopeia. Genome Biology, 21(1), 92. DOI ↗Redon, R., Ishikawa, S., Fitch, K. R., et al. (2006). Global variation in copy number in the human genome. Nature, 444(7118), 444–454. DOI ↗
نام‌های دیگرscPhylogeny, single-cell lineage tracing, clonal phylogenetics, single-cell tree inferenceCNV analysis, copy number variant detection, CNV calling, somatic copy number alteration analysis
مرتبط46
خلاصهSingle-cell phylogenetic analysis reconstructs evolutionary or developmental trees from single-cell sequencing data, tracing how individual cells diverged from a common ancestor. By leveraging somatic mutations, CRISPR-introduced barcodes, or copy-number changes as heritable characters, this method maps clonal relationships within tumors, developing tissues, or immune repertoires with unprecedented cellular resolution.Copy number variation (CNV) analysis is a genomic pipeline for detecting regions where individuals carry fewer or more copies of a DNA segment than the reference genome. CNVs span kilobases to megabases and are a major class of structural variation implicated in cancer, neurodevelopmental disorders, and population diversity. The pipeline typically processes SNP array intensities or read-depth signals from whole-genome sequencing, applies segmentation algorithms, calls gain and loss events, and annotates them against gene and clinical databases.
ScholarGateمجموعه‌داده
  1. v1
  2. 2 منابع
  3. PUBLISHED
  1. v1
  2. 2 منابع
  3. PUBLISHED

رفتن به جست‌وجو دریافت اسلایدها

ScholarGateمقایسهٔ روش‌ها: Single-cell Phylogenetic Analysis · Copy Number Variation Analysis. بازیابی‌شده در 2026-06-18 از https://scholargate.app/fa/compare