| load_manifest | R Documentation |
This dataset is a combination of the following two datasets from https://support.illumina.com/array/array_kits/humanomni5-4-beadchip-kit/downloads.html:
load_manifest()
A data frame with 4,327,108 rows (probes) and 18 variables:
Name of probe
Illumina ID of probe
rs number of probe
Chromosome
Address A of probe
Address B of probe
The possible bases of the SNP
TOP/BOT/PLUS/MINUS
TOP/BOT/PLUS/MINUS
The content of the .[.]. part of TopGenomicSeq (not included), including the flanking left and right parts
The left flanking of TopGenomicSeqSBE
The right flanking of TopGenomicSeqSBE
Bead set ID
3 or 2
+/-
II (only address A) or I (address A and B)
Signals whether SNP has alleles on same color channel (ambiguous) or not (unambiguous), or potentially is an INDEL (insertion/deletion): AMBiguous for AT-SNPs ([A/T] or [T/A]) and CG-SNPs; INDEL for INDELs; UNAMBiguous for the rest (e.g. AC-SNPs)
Some probes should be excluded (cf. above), this indicate those
InfiniumOmni5-4v1-2_A2.csv
Infinium Omni5-4 v1.2 Product Files -> Infinium Omni5-4 v1.2 Manifest File (CSV Format - GRCh38)
InfiniumOmni5-4v1-2_A1_b144_rsids.txt
Infinium Omni5-4 v1.2 Support Files -> Infinium Omni5-4 v1.2 Loci Name to rsID Conversion File
Note that the following probes have Exclude = FALSE (all others have Exclude = TRUE)
because they are ambiguous (SNP is C/G), but they are a Type-II probe (i.e. do not have an AddressB_ID),
so the bases cannot be distinguish as both C and G are detected by the green channel:
Name rs28362918 (Illumina ID rs28362918-131_T_R_1908372611)
Name rs28897688 (Illumina ID rs28897688-131_T_R_1908379219)
https://support.illumina.com/array/array_kits/humanomni5-4-beadchip-kit/downloads.html
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