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1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 f_cpdb_select_pathway <- function ( lc_res, grep_i_p_list= NULL ) { if ( is.null ( grep_i_p_list) ) { grep_i_p_list = list ( chemokines = "^CXCCCLCCRCX3XCLXCR" , th1 = "IL2IL12IL18IL27IFNGIL10TNF$TNF LTALTBSTAT1CCR5CXCR3IL12RB1IFNGR1TBX21STAT4" , th2 = "IL4IL5IL25IL10IL13AREGSTAT6GATA3IL4R" , th17 = "IL21IL22IL24IL26IL17AIL17AIL17FIL17RAIL10RORCRORASTAT3CCR4CCR6IL23RATGFB" , treg = "IL35IL10FOXP3IL2RATGFB" , costimulatory = "CD86CD80CD48LILRB2LILRB4TNFCD2ICAMSLAMLT[AB]NECTIN2CD40CD70CD27CD28CD58TSLPPVRCD44CD55CD[1-9]" , coinhibitory = "SIRPCD47ICOSTIGITCTLA4PDCD1CD274LAG3HAVCRVSIR" , niche = "CSF" ) } lc_res$ grep_i_p_list = list ( ) for ( name in names ( grep_i_p_list) ) { lc_res$ grep_i_p_list[[ name] ] = unique( grep( grep_i_p_list[[ name] ] , lc_res$ s_m_p$ interacting_pair, value = T ) ) } lc_res}
R
1 2 3 4 f_cpdb_select_cluster <- function ( lc_res, grep_celltype) { lc_res$ grep_celltype <- unique( grep( grep_celltype, lc_res$ s_m_p$ celltype, value = T ) ) lc_res}
R
1 2 3 4 5 6 7 8 9 10 11 f_cpdb <- function ( lc_res) { res <- lc_res$ s_m_p if ( ! is.null ( lc_res$ grep_i_p_list) ) { res <- res %>% dplyr:: filter( interacting_pair %in% reduce( lc_res$ grep_i_p_list, c ) ) } if ( ! is.null ( lc_res$ grep_celltype) ) { res <- res %>% dplyr:: filter( celltype %in% lc_res$ grep_celltype) } res}
R
示例1 2 3 4 5 6 7 sce <- f_readcellphoneDB( 'crpc_strom_epi_new' ) sce <- f_cpdb_select_cluster( sce, 'iCAF' ) grep_i_p_list = list ( vegf = "VEGFFGFIGF" ) sce <- f_cpdb_select_pathway( sce, grep_i_p_list) f_cDB_dotplot( f_cpdb( sce) )
R
cellphoneDB:筛选细胞和通路
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