hgu95av2MAP package:hgu95av2.db R Documentation _M_a_p _b_e_t_w_e_e_n _M_a_n_u_f_a_c_t_u_r_e_r _I_d_e_n_t_i_f_i_e_r_s _a_n_d _c_y_t_o_g_e_n_e_t_i_c _m_a_p_s/_b_a_n_d_s _D_e_s_c_r_i_p_t_i_o_n: hgu95av2MAP is an R object that provides mappings between manufacturer identifiers and cytoband locations. _D_e_t_a_i_l_s: Each manufacturer identifier is mapped to a vector of cytoband locations. The vector length may be one or longer, if there are multiple reported chromosomal locations for a given gene. An 'NA' is reported for any manufacturer identifiers that cannot be mapped to a cytoband at this time. Cytogenetic bands for most higher organisms are labeled p1, p2, p3, q1, q2, q3 (p and q are the p and q arms), etc., counting from the centromere out toward the telomeres. At higher resolutions, sub-bands can be seen within the bands. The sub-bands are also numbered from the centromere out toward the telomere. Thus, a label of 7q31.2 indicates that the band is on chromosome 7, q arm, band 3, sub-band 1, and sub-sub-band 2. The physical location of each band on a chromosome can be obtained from another object named "organism"CYTOLOC in a separate data package for human(humanCHRLOC), mouse(mouseCHRLOC), and rat(ratCHRLOC). Mappings were based on data provided by: Entrez Gene ( ftp://ftp.ncbi.nlm.nih.gov/gene/DATA ) on 2008-Apr2 _R_e_f_e_r_e_n_c_e_s: _E_x_a_m_p_l_e_s: x <- hgu95av2MAP # Get the probe identifiers that are mapped to any cytoband mapped_probes <- mappedkeys(x) # Convert to a list xx <- as.list(x[mapped_probes]) if(length(xx) > 0) { # Get the MAP for the first five probes xx[1:5] # Get the first one xx[[1]] }