# Calculating LOD from Olink® Explore data

#### Compiled: September 24, 2025

## Introduction

This tutorial describes how to use Olink® Analyze to integrate Limit of Detection (LOD) into Olink® Explore HT, Olink® Reveal, and Olink® Explore 384/3072 datasets. Although it is recommended to use all Olink Explore data in downstream analyses, LOD information can be useful when performing technical evaluations of a dataset.

In this tutorial, you will learn how to use `olink_lod()` to add LOD information to your Olink Explore dataset. Note that Olink Analyze does not contain example Olink Explore HT or Olink Explore 384/3072 datasets within the package, so external data will be necessary for the code below to work. The external data should contain internal and external controls for proper calculation and normalization. All file paths should be replaced with a path to your data and fixed LOD reference file (if applicable).

## Integrating LOD

Limit of Detection (LOD) is a metric that indicates the lowest measurable value of a protein. LOD can be helpful when performing technical evaluations of NPX™ datasets, such as calculating CVs. As a note, LOD is less important in downstream statistical analyses as values under LOD typically converge across groups. As such, including data below LOD is unlikely to increase the risk of false positive discoveries. Furthermore, data below LOD can be instrumental in downstream analyses such as biomarker discovery as a protein may be well expressed in one group and not measured in another group. In this case, this protein can be a strong biomarker candidate for specific groups.

LOD can be added to Olink Explore NPX datasets using `olink_lod()`. This function can calculate LOD from an NPX dataset using the dataset’s negative controls or a list of predetermined fixed LOD values (available in the Document Download Center at olink.com). As the default setting, `olink_lod()` will calculate LOD using a dataset’s negative controls.

Olink Explore data is commonly delivered plate control (PC) normalized or intensity normalized (the normalization type employed is indicated in the NPX file column Normalization), where the latter is dependent on that the analyzed samples are randomized. These are reported in the two respective columns PCNormalizedNPX and NPX. Please notice that for PC normalized datasets the content in these two columns will be identical, while for intensity normalized datasets the NPX column will include the intensity normalized values. Similarly, the `olink_lod()` function adds two columns to your dataset; PCNormalizedLOD and LOD respectively. For a PC normalized dataset the content in these two columns will be identical, while for an intensity normalized dataset the LOD column will contain intensity normalized LOD values. Examples of results for plate control and intensity normalization are shown in the tables below.

Example results from Plate Control Normalized Project
SampleID | SampleType | OlinkID | UniProt | Assay | Count | NPX | PCNormalizedNPX | Normalization | LOD | PCNormalizedLOD
--- | --- | --- | --- | --- | --- | --- | --- | --- | --- | ---
A1 | SAMPLE | OID01216 | O00533 | CHL1 | 1425 | 12.96 | 12.96 | Plate control | 2.37 | 2.37
A2 | SAMPLE | OID01216 | O00533 | CHL1 | 1240 | 11.27 | 11.27 | Plate control | 2.37 | 2.37
A3 | SAMPLE | OID01216 | O00533 | CHL1 | 2800 | 25.45 | 25.45 | Plate control | 2.37 | 2.37
A4 | SAMPLE | OID01216 | O00533 | CHL1 | 1590 | 14.45 | 14.45 | Plate control | 2.37 | 2.37
A5 | SAMPLE | OID01216 | O00533 | CHL1 | 839 | 7.63 | 7.63 | Plate control | 2.37 | 2.37
A6 | SAMPLE | OID01216 | O00533 | CHL1 | 695 | 6.32 | 6.32 | Plate control | 2.37 | 2.37

Example results from Intensity Normalized Project
SampleID | SampleType | OlinkID | UniProt | Assay | Count | NPX | PCNormalizedNPX | Normalization | LOD | PCNormalizedLOD
--- | --- | --- | --- | --- | --- | --- | --- | --- | --- | ---
A1 | SAMPLE | OID01216 | O00533 | CHL1 | 1425 | 17.12 | 12.96 | Intensity | 6.53 | 2.37
A2 | SAMPLE | OID01216 | O00533 | CHL1 | 1240 | 15.43 | 11.27 | Intensity | 6.53 | 2.37
A3 | SAMPLE | OID01216 | O00533 | CHL1 | 2800 | 29.61 | 25.45 | Intensity | 6.53 | 2.37
A4 | SAMPLE | OID01216 | O00533 | CHL1 | 1590 | 18.61 | 14.45 | Intensity | 6.53 | 2.37
A5 | SAMPLE | OID01216 | O00533 | CHL1 | 839 | 11.79 | 7.63 | Intensity | 6.53 | 2.37
A6 | SAMPLE | OID01216 | O00533 | CHL1 | 695 | 10.48 | 6.32 | Intensity | 6.53 | 2.37

## Import Olink Explore datasets

Olink Explore datasets are standard Olink Explore HT and Olink Explore 384/3072 NPX tables. The `read_NPX()` function can be used to import an NPX file in parquet form as generated by Olink Software. More information on using `read_NPX()` can be found in the Olink Analyze Overview tutorial.

    explore_npx <- read_NPX("~/Explore_NPX_file.parquet")

## Integrating Negative Control LOD

The negative control (NC) LOD method requires at least 10 negative controls in a dataset. Negative control data is available in the standard exported Explore HT and Explore 384/3072 NPX parquet files. NCs can be identified through the SampleID and SampleType columns.

A negative control will not contribute to the minimum number of required NCs if the negative control does not pass sample QC criteria (sample QC failure or warning) in all of the data (i.e. all Explore HT blocks, all Explore 3072 panels, or all Explore 384 panels that were measured)

Negative controls are used to calculate LOD from either PC normalized NPX or counts. For assays with more than 150 counts in one of the negative controls, LOD is calculated using the median PC normalized NPX and adding 3 standard deviations, or 0.2 NPX whichever is larger. For assays with fewer than 150 counts in all negative controls, LOD is calculated using the count values which are then converted into PC normalized NPX.

#### A note on calculating LOD from counts

Some assays will use count values as the LOD because the assay receives very few counts in the negative controls. For the convenience of data processing, the LOD in count values are converted to NPX values in the `olink_lod()` function. The LOD value for this assay (in counts) will become many LOD values in NPX (as extension control counts will vary across all samples). This is due to the fact that minor changes on the counts scale can result in significant changes on the NPX scale when working with small counts. The reason for this is that NPX is a relative scale, which is calculated by dividing the counts of the assay by the counts of the extension control. For example, given that the extension control values remain constant, if a count value were to change from 1 count to 2 counts, this would be a change of 1 NPX, while a change from 1000 counts to 1001 counts would be negligible on the NPX scale.

Furthermore, due to the low number of counts, the NPX values calculated from these counts do not correlate to true background levels. The converted NPX values should not be used as LOD values for these assays.

The resulting LOD is the PC normalized negative control LOD. In the event that the Explore dataset is intensity normalized, an intensity normalization adjustment factor is applied and the resulting intensity normalized LOD is reported in the LOD column and the PC normalized LOD is reported in the PCNormalizedLOD column.

    # Integrating negative control LOD for intensity normalized data
    explore_npx <- read_NPX("Path_to/Explore_NPX_file.parquet")
    olink_lod(explore_npx, lod_method = "NCLOD")

## Integrating Fixed LOD

The fixed LOD method uses fixed LOD values that have been calculated on negative controls used in Olink reference runs using the method described above for negative control LOD. These values are specific to the Data Analysis Reference ID, which can be found in your dataset. The fixed LOD data is available in an external CSV file which can be downloaded from the Document Download Center at olink.com. The fixed LOD values reported in this CSV file are the PC normalized LODs.

The fixed LOD file is read into the `olink_lod()` function to be integrated into an Explore dataset. In the event that the Explore dataset is intensity normalized, an intensity normalization adjustment factor is applied and the resulting intensity normalized LOD is reported in the LOD column and the PC normalized LOD is reported in the PCNormalizedLOD column.

    # Reading in Fixed LOD file path into R environment
    fixedLOD_filepath <- "Path_to/ExploreHT_fixedLOD.csv"

    # Integrating Fixed LOD for intensity normalized data
    explore_npx <- read_NPX("~/Explore_NPX_file.parquet")
    olink_lod(explore_npx, lod_file_path = fixedLOD_filepath, lod_method = "FixedLOD")

## When to use Fixed LOD vs NC LOD

For smaller sized studies (<10 NCs) we recommend using fixed LOD to integrate LOD values into your NPX dataset, as LOD calculations on fewer NCs may provide non-accurate values. However, it is important to keep in mind that fixed LOD values are not specific to your project, rather these values are generated by Olink when a new lot of reagents is released.

For larger projects we recommend calculating LOD from NC to obtain LOD values that are specific to your project. However, this requires that the dataset has at least 10 NCs with passing SampleQC.

## Integrating Both NC LOD and Fixed LOD

There is also the option to calculate both NC LOD and Fixed LOD for a data file by setting lod_method to “Both”. The resulting data will have 4 additional columns, starting with NC or Fixed to indicate the method used to calculate LOD, followed by LOD or PCNormalizedLOD as explained above. An example of the file format is shown below. Note that these columns will not automatically be recognized by other functions within Olink Analyze that use LOD (for example `olink_bridgeselector()`). To use these functions, the LOD value to be used should have “LOD” as the column name.

Example results using both LOD calculation methods
SampleID | SampleType | OlinkID | UniProt | Assay | Count | NPX | Normalization | PCNormalizedNPX | FixedLOD | FixedPCNormalizedLOD | NCLOD | NCPCNormalizedLOD
--- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | ---
A1 | SAMPLE | OID01216 | O00533 | CHL1 | 1425 | 17.12 | Intensity | 12.96 | 6.53 | 2.37 | 4.19 | 0.03
A2 | SAMPLE | OID01216 | O00533 | CHL1 | 1240 | 15.43 | Intensity | 11.27 | 6.53 | 2.37 | 4.19 | 0.03
A3 | SAMPLE | OID01216 | O00533 | CHL1 | 2800 | 29.61 | Intensity | 25.45 | 6.53 | 2.37 | 4.19 | 0.03
A4 | SAMPLE | OID01216 | O00533 | CHL1 | 1590 | 18.61 | Intensity | 14.45 | 6.53 | 2.37 | 4.19 | 0.03
A5 | SAMPLE | OID01216 | O00533 | CHL1 | 839 | 11.79 | Intensity | 7.63 | 6.53 | 2.37 | 4.19 | 0.03
A6 | SAMPLE | OID01216 | O00533 | CHL1 | 695 | 10.48 | Intensity | 6.32 | 6.53 | 2.37 | 4.19 | 0.03

## Adjusting LOD for Intensity Normalized Data

If an Olink Explore dataset is intensity normalized, a normalization adjustment factor is applied to the PC normalized LOD within the `olink_lod()` function.

For each assay, this adjustment factor is calculated as the median NPX of all samples (excluding Olink’s external controls) within each plate. For Olink Explore 3072, overlapping assays are assessed separately, within their respective panels. The intensity normalized negative control LOD is calculated by subtracting this adjustment factor from the PC normalized negative control LOD.

The intensity normalization LOD adjustment is applied to both the negative control and fixed LOD methods.

## Export Olink Explore Data with LOD

Olink Explore data with LOD data can be exported using arrow::write_parquet to export Olink Explore data as a parquet file in long format.

    # Exporting Olink Explore data with LOD information as a parquet file
    explore_npx <- read_NPX("Path_to/Explore_NPX_file.parquet")

    explore_npx_NC_LOD <- explore_npx %>%
      olink_lod(lod_method = "NCLOD")

    # Add metadata for export
    df <- explore_npx_NC_LOD |>
      arrow::as_arrow_table()

    df$metadata$FileVersion <- "NA"
    df$metadata$ExploreVersion <- "NA"
    df$metadata$ProjectName <- "NA"
    df$metadata$SampleMatrix <- "NA"
    df$metadata$DataFileType <- "Olink Analyze Export File"
    df$metadata$ProductType <- "ExploreHT" # "ExploreHT", "Explore3072", or "Reveal"
    df$metadata$Product <- "ExploreHT" # "ExploreHT", "Explore3072", or "Reveal"

    arrow::write_parquet(x = df, sink = "path_to_output.parquet")

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