Allele-specific multi-sample copy number segmentation in ASCAT

被引:16
|
作者
Ross, Edith M. [1 ]
Haase, Kerstin [2 ]
Van Loo, Peter [2 ]
Markowetz, Florian [1 ]
机构
[1] Univ Cambridge, Canc Res UK Cambridge Inst, Cambridge CB2 0RE, England
[2] Francis Crick Inst, London NW1 1AT, England
基金
英国医学研究理事会; 英国惠康基金;
关键词
D O I
10.1093/bioinformatics/btaa538
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: Allele-specific copy number alterations are commonly used to trace the evolution of tumours. A key step of the analysis is to segment genomic data into regions of constant copy number. For precise phylogenetic inference, breakpoints shared between samples need to be aligned to each other. Results: Here, we present asmultipcf, an algorithm for allele-specific segmentation of multiple samples that infers private and shared segment boundaries of phylogenetically related samples. The output of this algorithm can directly be used for allele-specific copy number calling using ASCAT.
引用
收藏
页码:1909 / 1911
页数:3
相关论文
共 50 条
  • [21] Inferring allele-specific copy number aberrations and tumor phylogeography from spatially resolved transcriptomics
    Ma, Cong
    Balaban, Metin
    Liu, Jingxian
    Chen, Siqi
    Ding, Li
    Raphael, Benjamin J.
    CANCER RESEARCH, 2024, 84 (06)
  • [22] Patchwork: allele-specific copy number analysis of whole-genome sequenced tumor tissue
    Markus Mayrhofer
    Sebastian DiLorenzo
    Anders Isaksson
    Genome Biology, 14
  • [23] CYP2D6 Allele-Specific Copy Number Determination by Digital PCR
    Wang, Wendy
    Boone, Erin
    Lin, Lancy
    Stevens, Junko
    Gaedigk, Andrea
    PHARMACOGENETICS AND GENOMICS, 2025, 35 (01): : 15 - 16
  • [24] Inferring Allele-Specific Copy Number Aberrations and Tumor Phylogeography from Spatially Resolved Transcriptomics
    Ma, Cong
    Balaban, Metin
    Liu, Jingxian
    Chen, Siqi
    Ding, Li
    Raphael, Benjamin J.
    RESEARCH IN COMPUTATIONAL MOLECULAR BIOLOGY, RECOMB 2024, 2024, 14758 : 466 - 469
  • [25] Inferring allele-specific copy number aberrations and tumor phylogeography from spatially resolved transcriptomics
    Ma, Cong
    Balaban, Metin
    Liu, Jingxian
    Chen, Siqi
    Wilson, Michael J.
    Sun, Christopher H.
    Ding, Li
    Raphael, Benjamin J.
    NATURE METHODS, 2024, 21 (12) : 2239 - 2247
  • [26] Patchwork: allele-specific copy number analysis of whole-genome sequenced tumor tissue
    Mayrhofer, Markus
    DiLorenzo, Sebastian
    Isaksson, Anders
    GENOME BIOLOGY, 2013, 14 (03):
  • [27] Integrative single-cell analysis of allele-specific copy number alterations and chromatin accessibility in cancer
    Wu, Chi-Yun
    Lau, Billy T.
    Kim, Heon Seok
    Sathe, Anuja
    Grimes, Susan M.
    Ji, Hanlee P.
    Zhang, Nancy R.
    NATURE BIOTECHNOLOGY, 2021, 39 (10) : 1259 - +
  • [28] Bamgineer: Introduction of simulated allele-specific copy number variants into exome and targeted sequence data sets
    Samadian, Soroush
    Bruce, Jeff P.
    Pugh, Trevor J.
    PLOS COMPUTATIONAL BIOLOGY, 2018, 14 (03)
  • [29] Integrative single-cell analysis of allele-specific copy number alterations and chromatin accessibility in cancer
    Chi-Yun Wu
    Billy T. Lau
    Heon Seok Kim
    Anuja Sathe
    Susan M. Grimes
    Hanlee P. Ji
    Nancy R. Zhang
    Nature Biotechnology, 2021, 39 : 1259 - 1269
  • [30] Robust analysis of allele-specific copy number alterations from scRNA-seq data with XClone
    Huang, Rongting
    Huang, Xianjie
    Tong, Yin
    Yan, Helen Y. N.
    Leung, Suet Yi
    Stegle, Oliver
    Huang, Yuanhua
    NATURE COMMUNICATIONS, 2024, 15 (01)